Abstract
Many visualization techniques are available to explore the cardiovascular system from usual ultrasound echography and velocimetry, multislice spiral computed tomography particularly for cardiac imaging, and magnetic resonance imaging for blood flow assessment, to magnetocardiography, diode laser, and optical coherence tomography. Functional magnetic resonance imaging is based on increased blood flow gushing in target regions that are responding to imposed stimuli. Ultrasound scattering from Rayleigh fractal aggregates is proposed for imaging flow dynamics of deformable or hardened red cell clusters in dense suspension.
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Notes
- 1.
The wavelength is reduced in the human body according to the permittivity and conductivity of crossed tissues.
- 2.
Diffusion of water within a tissue excited by a magnetic field gradient causes MRI signal attenuation. The eigenvectors and eigenvalues of the voxel-averaged diffusion tensor specify the principal directions and rates of water diffusion in each voxel of the tissue image. The eigenvector corresponding to the maximum eigenvalue of the diffusion tensor points in the direction of maximum rate of diffusion assumed to be the direction of the axis of a cylindrical fiber. The orientation of the eigenvectors can be defined by inclination and transverse angles. The inclination angle of the myofiber is the angle between: (1) the intersection line of the image plane and the plane parallel to the epicardial tangent plane at the corresponding azimuthal position (tangent plane); and (2) the projection of the eigenvector onto the tangent plane. The transverse angle is the angle between: (1) the intersection line, and (2) the projection of the eigenvector onto the image plane. The correlation has been checked by experiments performed in an excised portion of the right ventricle by comparison of DTMRI and histology myofiber angles [23, 24], but DTMRI time and space resolutions, especially in vivo, were too large to get an accurate map of myofiber angles. More recently, space resolution of 310 to 390 μm in the slice plane with a slice thickness of 0.8 to 1 mm has been obtained in isolated dog hearts [25]. These authors extract 2 local angles, the myofiber main axis angle and the cross-sheet (from endocardium to epicardium) angle. The myofiber angle is defined by the angle between the local circumferential tangent vector of the reconstructed mesh of the heart wall and projection of the primary eigenvector of the voxel-related water diffusion tensor onto the epicardial tangent plane. The cross-sheet angle is determined by the radial vector and the projection of the tertiary eigenvector of the diffusion tensor, which is parallel to the cardiac sheet normal, onto the plane defined by the radial and circumferential vectors. Images can be obtained using a slice-selection fast spin-echo diffusion-weighted technique coupled with gradient recalled acquisition in the steady-state (GRASS) imaging mode to define epicardial and endocardial surfaces [26].
- 3.
The diffusivities along the 3 principal axes of the ellipsoid.
- 4.
The displacement of the aortic valve has been estimated to be equal to 15–20 mm.
- 5.
Comb excitation enables simultaneous tagging in multiple parallel planes during breathhold.
- 6.
IVUS-based virtual histology results from signal processing by autoregressive spectral analysis of radiofrequency ultrasound backscatter signals to assess plaque composition that is not complex. However, necrotic cores that surround calcified zones can be artefacts. Wavelet analysis of radiofrequency US signals represents an alternative modality.
- 7.
Displacement of the tissue between 2 images can be used to assess the bulk rheology of a region of interest of the explored tissue. Elastographic scanning maps strain magnitude (image brightness) and sign (color hue associated with compression or distention, for instance).
- 8.
Broad bandwidth lights can be generated from superluminescent diodes or femtosecond laser pulses.
- 9.
IVUS technique has a 100 μm axial resolution.
- 10.
Elastin serves as the axial backbone of alveolar ducts and alveolar entrances. It also resides in the sheath of extraalveolar microvessels.
- 11.
Vessel bore and wall smoothness depend on the threshold.
- 12.
The snakes are dilated by external and internal forces using a finite element method to solve the minimization problem, only taking into account the suitable edge points that have been extracted by an edge detector.
- 13.
The contour is then defined as the location of the maxima of the gradient of the image intensity in the gradient direction. Vascular modeling relies on the assumption of a Gaussian intensity profile with a first derivative maximal at the vessel wall and a second derivative maximal on the vessel axis, the vessel being supposed to have a circular cross section. When the vessel axis is determined and local radii are estimated, the vessel wall is reconstructed.
- 14.
In straight pipes, the axial pressure difference, which varies either nonlinearly in the entry length or linearly when the flow is fully developed, is exhibited in any duct section that is not normal to the centerline.
- 15.
The surface element size depends on the local surface curvature. The stronger the curvature, the smaller the size.
- 16.
Quickly varying pressures must be measured by transducers, which convert pressures into electrical signals, able to accurately sense high frequencies. Sensitivity, linear output for the whole pressure range, suitable frequency response, and spatial resolution are the main features of transducers. In particular, the transducer size must be smaller than the distance over which exist spatial pressure variations.
- 17.
The nonlinear soliton equation was developed by D.J. Korteweg and G. de Vries at the end of the nineteenth century. The nonlinear term balances the dispersion. The existence and uniqueness of solution to the Cauchy problem for the nonlinear Korteweg–de Vries equation and local controllability around the origin given by the nonlinear term has been proved [93]. Signal processing using progressive wave speed analysis is more appropriate than employing frequency analysis suitable for stationary waves.
- 18.
The soliton is a wave that propagates without dispersion. Solitons interact without losing their identity, keeping shape and amplitude. An n-soliton solution refers to n components of different amplitude that interact. The propagation speed is proportional to wave amplitude. The higher the amplitude, the faster the propagation. Soliton solutions are used to model fast dynamics of pressure wave propagation and an associated windkessel model to take slow dynamics into account.
- 19.
The second wave of the 2-soliton model is associated with the dicrotic wave due to the aortic valve closure. The 3-soliton model is used to fit bifid pressure waves. A bifid curve exhibits an incisure in the ascending systolic part near the peak value rather than an usual monotonic soaring aspect.
- 20.
- 21.
The resistivity of the lungs is approximately 20 times that of the blood.
- 22.
The resistivity of bones increases about a 100-fold with respect to blood.
- 23.
Electric and magnetic leads are different. The signal-to-noise ratio for the electrical and magnetic recordings are affected by different factors. Although the electrical resistivity of the lung parenchyma is relatively high, the magnetic permeability of body tissues resembles that of a free space, allowing easy recordings from the posterior face of the thorax.
- 24.
Magnetocardiographic signals have been computed using a model with a source represented by an uniform double layer and with a heterogeneous, multicompartmental model of the thorax, the geometry of which is derived from magnetic resonance imaging [124]. Computed and measured magnetic signals were in good agreement. The magnetocardiogram and electrocardiogram have a common basis.
- 25.
The propagation speed of sound waves at 310 K is equal to 354, 357, and 352 m/s in partially humidified air, in air saturated with water vapor, and in exhaled air, respectively.
- 26.
\(\upsigma _{t}^{2}\, \propto \,\overline{\mathcal{D}}_{\mathrm{app}}\bar{t}/V _{q}^{2}\), where \(\mathcal{D}_{\mathrm{app}}/\mathcal{D}\ =\ \kappa \mathrm{Pe}_{T}^{2}\) (Pe T : Péclet number in the trachea) varies according to literature data both at inspiration (1.1–1.5) and expiration (0.4–0.5) [132, 133].
- 27.
The association speed of carbon monoxide on hemoglobin is slower than that of oxygen, but its dissociation rate is a thousand times slower than its association rate. Carbon monoxide is thus said to have a high affinity for hemoglobin.
- 28.
The usual tracer is radiolabeled diethylenetriaminepentaacetic acid (DTPA).
- 29.
The clearance \((dQ/dt)/cV\) (dimension: T −1) is the flux of tracer (dQ∕dt, Q: substance quantity) divided by the luminal tracer content, the latter being the product of tracer luminal concentration c by volume V of airway surface film, itself the product of the airway surface area (tracer uptake area) by the liquid film thickness. The uptake rate can also be evaluated from the decay rate constant, assuming a monoexponential relationship with time, although the clearance can follow a biexponential evolution. The clearance of DTPA from human lungs ranges 0.59–1.56.10−2/s, with a mean of about 10−2/s, varying with the aerosol size and the working group [142].
- 30.
The population comprises 114 volunteers, 27 to 58-yr old, with 15 nonsmokers, and 43 ex-smokers. Smoking habits have been defined according to the amount (1 cigar being equivalent to 5 cigarettes, 1 cigarillo to 2 cigarettes, 1 g of tabacco to 1 cigarette), to the quality (with or without smoke inhalation), ex-smokers being subdivided into 2 groups whether they have stopped more than one month or more than one year. Slight smokers were defined by less than 5 cigarettes per day over any period of time or more than 5 cigarettes per day for less than one year. Smokers include 2 categories, according to the existence of respiratory symptoms.
- 31.
Transit time moments are computed using the entire maneuver. They then depend on the effort performed at the end of the test. Forced expirations terminate more or less prematurely, at unrepeatable times in a given subject. A better repeatability is obtained using truncated spirograms. The values then strongly depend on the arbitrary chosen threshold.
References
Introduction
Bachelard G (1938 [1969]) La psychanalyse du feu [The Psychoanalysis of Fire]. Gallimard, Paris
Chap. 1. Anatomy of the Cardiovascular System
Echtler K, Stark K, Lorenz M, Kerstan S, Walch A, Jennen L, Rudelius M, Seidl S, Kremmer E, Emambokus NR, von Bruehl ML, Frampton J, Isermann B, Genzel-Boroviczny O, Schreiber C, Mehilli J, Kastrati A, Schwaiger M, Shivdasani RA, Massberg S (2010) Platelets contribute to postnatal occlusion of the ductus arteriosus. Nature – Medicine 16:75–82
Hong Z, Kutty S, Toth PT, Marsboom G, Hammel JM, Chamberlain C, Ryan JJ, Zhang HJ, Sharp WW, Morrow E, Trivedi K, Weir EK, Archer SL (2013) Role of dynamin-related protein 1 (drp1)-mediated mitochondrial fission in oxygen sensing and constriction of the ductus arteriosus. Circulation Research 112:802–815
Gray H (1995) Gray’s anatomy: anatomy descriptive and surgical. Barnes and Noble, New York
Rouvire H, Delmas A (2002) Anatomie humaine descriptive, topographique et fonctionnelle [Descriptive, Topographical, and Functional Human Anatomy], Vols. I–IV. Masson, Paris
Iacobellis G, Corradi D, Sharma AM (2005) Epicardial adipose tissue: anatomic, biomolecular and clinical relationships with the heart. Nature – Clinical Practice Cardiovascular Medicine 2:536–543.
Badano LP, Agricola E, Perez de Isla L, Gianfagna P, Zamorano JL (2009) Evaluation of the tricuspid valve morphology and function by transthoracic real-time three-dimensional echocardiography. European Journal of Echocardiography 10:477–484
Kozlowski D, Owerczuk A, Piwko G, Kozlowska M, Bigus K, Grzybiak M (2002) The topography of the subthebesian fossa in relation to neighbouring structures within the right atrium. Folia Morphologica 62:65–70
Stradins P, Lacis R, Ozolanta I, Purina B, Ose V, Feldmane L, Kasyanov V (2004) Comparison of biomechanical and structural properties between human aortic and pulmonary valve. European Journal of Cardio-thoracic Surgery 26:634–639
Keith A, Flack M (1907) The form and nature of the muscular connections between the primary divisions of the vertebrate heart. Journal of Anatomy and Physiology 41:172–189
Anderson RH, Razavi R, Taylor AM (2004) Cardiac anatomy revisited. Journal of Anatomy 205:159–177
Anderson RH, Webb S, Brown NA (1999) Clinical anatomy of the atrial septum with reference to its developmental components. Clinical Anatomy 12:362–374
Staszewsky L, Latini R (2013) What is the atrium trying to tell us? European Heart Journal 34:255-257
Gupta S, Matulevicius SA, Ayers CR, Berry JD, Patel PC, Markham DW, Levine BD, Chin KM, de Lemos JA, Peshock RM, Drazner MH (2013) Left atrial maximal volume and left atrial emptying fraction as predictors of cardiovascular events in community-based or population studies. European Heart Journal 34:278–285
Swanson WM, Clark RE (1974) Dimensions and geometric relationships of the human aortic valve as a function of pressure. Circulation Research 35:871–882
Grande KJ, Kunzelman KS, Cochran RP, David TE, Verrier ED (1993) Porcine aortic leaflet arrangement may contribute to clinical xenograft failure. ASAIO Journal 39:918–922
Bäck M, Gasser TC, Michel JB, Caligiuri G (2013) Biomechanical factors in the biology of aortic wall and aortic valve diseases. Cardiovascular Research 99:232–241
Valsalva AM (1740) Opera. Venice
Bellhouse BJ (1969) Velocity and pressure distributions in the aortic valve. Journal of Fluid Mechanics 37:587–600
Jatene MB, Monteiro R, Guimaraes MH, Veronezi SC, Koike MK, Jatene FB, Jatene AD (1999) Aortic valve assessment. Anatomical study of 100 healthy human hearts. Arquivos Brasileiros de Cardiologia 73:81-86
Tank PW, Gross Anatomy, Department of Neurobiology and Developmental Sciences, University of Arkansas for Medical Sciences, http://anatomy.uams.edu/anatomyhtml/heart2.html
Jiamsripong P, Honda T, Reuss CS, Hurst RT, Chaliki HP, Grill DE, Schneck SL, Tyler R, Khandheria BK, Lester SJ (2007) Three methods for evaluation of left atrial volume. European Journal of Echocardiography 9:351–355
Herregods MC, De Paep G, Bijnens B, Bogaert JG, Rademakers FE, Bosmans HT, Bellon EP, Marchal GJ, Baert AL, Van de Werf F, De Geest H (1994) Determination of left ventricular volume by two-dimensional echocardiography: comparison with magnetic resonance imaging. European Heart Journal 15:1070–1073
Armour JA (2008) Potential clinical relevance of the ’little brain’ on the mammalian heart. Experimental Physiology 93:165–176
Gray AL, Johnson TA, Ardell JL, Massari VJ (2004) Parasympathetic control of the heart. II. A novel interganglionic intrinsic cardiac circuit mediates neural control of heart rate. Journal of Applied Physiology 96:2273–2278
Waldmann M, Thompson GW, Kember GC, Ardell JL, Armour JA (2006) Stochastic behavior of atrial and ventricular intrinsic cardiac neurons. Journal of Applied Physiology 101:413–419
Sharma V (2009) Deterministic chaos and fractal complexity in the dynamics of cardiovascular behavior: perspectives on a new frontier. Open Cardiovascular Medicine Journal 3:110–123
Avnir D, Biham O, Lidnar D, Malcai O (1998) Is the geometry of nature fractal? Science 279:39–40
Kleiber M (1947) Body size and metabolic rate. Physiological Reviews 27:511–541
West GB, Brown JH, Enquist BJ (1997) A general model for the origin of allometric scaling laws in biology. Science 276:122–126
Sapoval B, Gobron T, Margolina A (1991) Vibrations of fractal drums. Physical Review Letters 67:2974–2977
D’Arcy Thompson W (1917) On Growth and Form. Cambridge University Press, Cambridge, UK
Van Vliet P, Wu SM, Zaffran S, Pucéat M (2012) Early cardiac development: a view from stem cells to embryos. Cardiovascular Research 96:352–362
Senyo SE, Steinhauser ML, Pizzimenti CL, Yang VK, Cai L, Wang M, Wu TD, Guerquin-Kern JL, Lechene CP, Lee RT (2013) Mammalian heart renewal by pre-existing cardiomyocytes. Nature 493:433–436
Mercola M (2012) Cardiovascular biology: A boost for heart regeneration. Nature 492: 360–362
Eulalio A, Mano M, Dal Ferro M, Zentilin L, Sinagra G, Zacchigna S, Giacca M (2012) Functional screening identifies miRNAs inducing cardiac regeneration. Nature 492:376–381
Chien KR, Domian IJ, Parker KK (2008) Cardiogenesis and the complex biology of regenerative cardiovascular medicine. Science 322:1494–1497
Smart N, Riley PR (2009) Derivation of epicardium-derived progenitor cells (EPDCs) from adult epicardium. Current Protocols in Stem Cell Biology 2:unit2c.2
Zhou B, Ma Q, Rajagopal S, Wu SM, Domian I, Rivera-Feliciano J, Jiang D, von Gise A, Ikeda S, Chien KR, Pu WT (2008) Epicardial progenitors contribute to the cardiomyocyte lineage in the developing heart. Nature 454:109–113
Wagner KD, Wagner N, Schedl A (2003) The complex life of WT1. Journal of Cell Science 116:1653–1658
Wagner KD, Wagner N, Bondke A, Nafz B, Flemming B, Theres H, Scholz H (2002) The Wilms’ tumor suppressor Wt1 is expressed in the coronary vasculature after myocardial infarction. FASEB Journal 16:1117–1119
Koninckx R, Daniëls A, Windmolders S, Mees U, Macianskiene R, Mubagwa K, Steels P, Jamaer L, Dubois J, Robic B, Hendrikx M, Rummens JL, Hensen K (2013) The cardiac atrial appendage stem cell: a new and promising candidate for myocardial repair. Cardiovascular Research 97:413–423
Nam YJ, Song K, Luo X, Daniel E, Lambeth K, West K, Hill JA, DiMaio JM, Baker LA, Bassel-Duby R, Olson EN (2013) Reprogramming of human fibroblasts toward a cardiac fate. Proceedings of the National Academy of Sciences of the United States of America 110:5588–5593
Mulligan-Kehoe MJ (2010) The vasa vasorum in diseased and nondiseased arteries. American Journal of Physiology – Heart and Circulatory Physiology 298:H295–H305
Chambers R, Zweifach BW (1994) Topography and function of the mesenteric capillary circulation. American Journal of Anatomy 75:175–205
Lee JS (2000) Biomechanics of the microcirculation, an integrative and therapeutic perspective. Annals of Biomedical Engineering 28:1–13
Hilgers RHP, Schiffers PMH, Aartsen WM, Fazzi GE, Smits JFM, De Mey JGR (2004) Tissue angiotensin-converting enzyme in imposed and physiological flow-related arterial remodeling in mice. Arteriosclerosis, Thrombosis, and Vascular Biology 24:892–897
Batra S, Rakusan K (1992) Capillary length, tortuosity, and spacing in rat myocardium during cardiac cycle. American Journal of Physiology – Heart and Circulatory Physiology 263:H1369–H1376
Hudlicka O, Tyler KR (1984) The effect of long-term high-frequency stimulation on capillary density and fibre types in rabbit fast muscles. Journal of Physiology 353:435–445
Krenz GS, Lin J, Dawson CA, Linehan JH (1994) Impact of parallel heterogeneity on a continuum model of the pulmonary arterial tree. Journal of Applied Physiology 77:660–670
Marxen M, Henkelman RM (2003) Branching tree model with fractal vascular resistance explains fractal perfusion heterogeneity. American Journal of Physiology – Heart and Circulatory Physiology 284:H1848–H1857
Liew G, Mitchell P, Rochtchina E, Wong TY, Hsu W, Lee ML, Wainwright A, Wang JJ (2003) Fractal analysis of retinal microvasculature and coronary heart disease mortality. European Heart Journal 32:422–429
Schelin AB, Károlyi G, de Moura AP, Booth NA, Grebogi C (2010) Fractal structures in stenoses and aneurysms in blood vessels. Philosophical Transactions of the Royal Society – London – A Mathematical, Physical, and Engineering sciences 368:5605–5617
Bassingthwaighte JB, King RB, Roger SA (1989) Fractal nature of regional myocardial blood flow heterogeneity. Circulation Research 65:578–590
Karch R, Neumann F, Podesser BK, Neumann M, Szawlowski P, Schreiner W (2003) Fractal properties of perfusion heterogeneity in optimized arterial trees: a model study. Journal of General Physiology 122:307–321
Kurz H, Sandau K (1998) Allometric scaling in biology. Science 281:751
Kurz H, Wilting J, Sandau K, Christ B (1998) Automated evaluation of angiogenic effects mediated by VEGF and PlGF homo- and heterodimers. Microvascular Research 55:92–102
Mori D, Yamaguchi T (2002) Computational fluid dynamics modeling and analysis of the effect of 3-D distortion of the human aortic arch. Computer Methods in Biomechanics and Biomedical Engineering 5:249–260
Ruddy JM, Jones JA, Spinale FG, Ikonomidis JS (2008) Regional heterogeneity within the aorta: relevance to aneurysm disease. Journal of Thoracic and Cardiovascular Surgery 136:1123–1130
Cebral JR (2005) www.scs.gmu.edu/∼jcebral/
Bouthillier A, van Loveren HR, Keller JT (1996) Segments of the internal carotid artery: a new classification. Neurosurgery 38:425–432
Schaller B (2004) Physiology of cerebral venous blood flow: from experimental data in animals to normal function in humans. Brain Research Reviews 46:243–260
Harmon JV, Edwards WD (1987) Venous valves in subclavian and internal jugular veins. Frequency, position, and structure in 100 autopsy cases. American Journal of Cardiovascular Pathology 1:51–54
Henry JL, Calaresu FR (1974) Excitatory and inhibitory inputs from medullary nuclei projecting to spinal cardioacceleratory neurons in the cat. Experimental Brain Research 20:485–504
Hildebrandt JR (1974) Central connections of aortic depressor and carotid sinus nerves. Experimental Neurology 45:590–605
Gebber GL, Taylor DG, Weaver LC (1973) Electrophysiological studies on organization of central vasopressor pathways. American Journal of Physiology 224:470–481
Snyder DW, Gebber GL (1973) Relationships between medullary depressor region and central vasopressor pathways. American Journal of Physiology 225:1129–1137
Weaver LC, Gebber GL (1974) Electrophysiological analysis of neural events accompanying active dilatation. American Journal of Physiology 226:84–89
Abboud FM (2010) In search of autonomic balance: the good, the bad, and the ugly. American Journal of Physiology — Regulatory, Integrative and Comparative Physiology 298:R1449–R1467
Klabunde RE (2011) Cardiovascular Physiology Concepts, 2nd edition, Wolters Kluwer – Lippincott Williams and Wilkins, Philadelphia, Pennsylvania
Prabhakar NR, Peng YJ (2004) Peripheral chemoreceptors in health and disease. Journal of Applied Physiology 96:359–366
Schultz HD, Li YL (2007) Carotid body function in heart failure. Respiratory Physiology and Neurobiology 157:171–185
Eyzaguirre C (2007) Electric synapses in the carotid body–nerve complex. Respiratory Physiology and Neurobiology 157:116–122
De Castro F (1928) Sur la structure et l’innervation du sinus carotidien de l’homme et des mammifères. Nouveaux faits sur l’innervation et la fonction du glomus caroticum. [On the structure and innervation of carotid sinus in humans and mammals. New facts on innervation and function of the glomus caroticum.] Travaux du Laboratoire de Recherches en Biologie 25:331–380
Kummer W, Gibbins IL, Heym C (1989) Peptidergic innervation of arterial chemoreceptors. Archives of Histology and Cytology 52:361–364
Rey S, Del Rio R, Alcayaga J, Iturriaga R (2006) Endothelins in the cat petrosal ganglion and carotid body: effects and immunolocalization. Brain Research 1069:154–158
Prabhakar NR (2000) Oxygen sensing by the carotid body chemoreceptors. Journal of Applied Physiology 88:2287–2295
Schultz HD, Li YL, Ding Y (2007) Arterial chemoreceptors and sympathetic nerve activity: implications for hypertension and heart failure. Hypertension 50:6–13
Molenda O (1975) Morphology and topography of the carotid body and carotid sinus in sheep. Polskie Archiwum Weterynaryjne 18:343–364
Sadik AH, Al-Shaikhly AK, Khamas WA (1993) Anatomic location of the carotid body and carotid sinus in sheep and goats. Small Ruminant Research 12:371–377
Peng YJ, Nanduri J, Raghuraman G, Souvannakitti D, Gadalla MM, Kumar GK, Snyder SH, Prabhakar NR (2010) H2S mediates O2 sensing in the carotid body. Proceedings of the National Academy of Sciences of the United States of America 107:10719–10724
Doan TN, Stephans K, Ramirez AN, Glazebrook PA, Andresen MC, Kunze DL (2004) Differential distribution and function of hyperpolarization-activated channels in sensory neurons and mechanosensitive fibers. Journal of Neuroscience 24:3335–3343
Chap.2. Anatomy of the Ventilatory Apparatus
Ochs M, Nyengaard JR, Jung A, Knudsen L, Voigt M, Wahlers T, Richter J, Gundersen HJ (2004) The number of alveoli in the human lung. American Journal of Respiratory and Critical Care Medicine 169:120–124
Horsfield K (1978) Morphometry of the small pulmonary arteries in man. Circulation Research 42:593–597
Glenny RW (2011) Emergence of matched airway and vascular trees from fractal rules. Journal of Applied Physiology 110:1119–1129
Fetita C, Mancini S, Perchet D, Prêteux F, Thiriet M, Vial L (2005) An image-based computational model of oscillatory flow in the proximal part of tracheobronchial trees. Computer Methods in Biomechanics and Biomedical Engineering 8:279–293
Christophe JJ, Ishikawa T, Matsuki N, Imai Y, Takase K, Thiriet M, Yamaguchi T (2010) Patient-specific morphological and blood flow analysis of pulmonary artery in the case of severe deformations of the lung due to pneumothorax. Journal of Biomechanical Science and Engineering 5:485–498
Robinson RJ, Russo J, Doolittle RL (2009) 3D airway reconstruction using visible human data set and human casts with comparison to morphometric data. Anatomical Record – Advances in Integrative Anatomy and Evolutionary Biology 292:1028–1044
Guyton AC (1985) Anatomy and Physiology, Saunders College Publishing, New York
Golde AR (2006) Rhinoplastic techniques for the nasal valve for the patient with sleep apnea. Operative Techniques in Otolaryngology-Head and Neck Surgery 17:242–251
Haight JS, Cole P (1983) The site and function of the nasal valve. Laryngoscope 93:49–55
Martínez MM, Román LJ, C Villalobos (2004) Biofluid dynamics of the ear–nose–throat system. Congress on Biofluid Dynamics of Human Body Systems at University of Puerto Rico, Mayagëz
Bachmann W, Legler U (1972) Studies on the structure and function of the anterior section of the nose by means of luminal impressions. Acta Oto-Laryngologica 73:433–442
Ingels KJ, Meeuwsen F, van Strien HL, Graamans K, Huizing EH (1990) Ciliary beat frequency and the nasal cycle, European Archives of Otorhinolaryngology 248:123–126
Sappey MPC (1867–1874) Traité d’anatomie descriptive (Treatise of Descriptive Anatomy), Paris; and Sappey MPC (1879) Atlas d’Anatomie Descriptive (Atlas of Descriptive Anatomy), Paris (see also “The Larynx – Gray’s Anatomy of the Human Body” Yahoo – Education. education.yahoo.com/reference/gray/subjects/subject/236)
Begis D, Delpuech C, Le Tallec P, Loth L, Thiriet M, Vidrascu M (1988) A finite-element model of tracheal collapse. Journal of Applied Physiology 64:1359–1368
Thiriet M (1994) Etude des écoulements dans les voies aériennes proximales et les artères de gros calibre. Mémoire pour l’habilitation à diriger des recherches, UFR de physique, Université Paris VII. (Study of flows in proximal airways and large arteries. Thesis for Accreditation to Supervise Research, Paris Diderot University)
Thiriet M, Maarek JM, Chartrand DA, Delpuech C, Davis L, Hatzfeld C, Chang HK (1989) Transverse images of the human thoracic trachea during forced expiration. Journal of Applied Physiology 67:1032–1040
Rhodin J, Dalhamn T (1956) Electron microscopy of the tracheal ciliated mucosa in rat. Zeitschrift für Zellforschung und mikroskopische Anatomie 44:345–412
Reinhardt JM, Ding K, Cao K, Christensen GE, Hoffman EA, Bodas SV (2008) Registration-based estimates of local lung tissue expansion compared to xenon CT measures of specific ventilation. Medical Image Analysis 12:752–763
Ukil S, Reinhardt JM (2009) Anatomy-guided lung lobe segmentation in X-ray CT images. IEEE Transactions on Medical Imaging 28:202–214
Miserocchi G (1997) Physiology and pathophysiology of pleural fluid turnover. European Respiratory Journal 10:219–225
Vasilescu DM, Gao Z, Saha PK, Yin L, Wang G, Haefeli-Bleuer B, Ochs M, Weibel ER, Hoffman EA (2012) Assessment of morphometry of pulmonary acini in mouse lungs by nondestructive imaging using multiscale microcomputed tomography. Proceedings of the National Academy of Sciences of the United States of America 109:17105–17110
Bucher U, Reid L (1961) Development of the intrasegmental bronchial tree: the pattern of branching and development of cartilage at various stages of intra-uterine life. Thorax 16:207–218
Sera T, Uesugi K, Yagi N (2005) Localized morphometric deformations of small airways and alveoli in intact mouse lungs under quasi-static inflation. Respiratory Physiology and Neurobiology 147:51–63
Weibel ER (1963) Morphometry of the human lung, Academic Press, New York
Choi J, Tawhai MH, Hoffman EA, Lin CL (2009) On intra- and intersubject variabilities of airflow in the human lungs. Physics of Fluids 21:101901
Lin CL, Tawhai MH, McLennan G, Hoffman EA (2007) Characteristics of the turbulent laryngeal jet and its effect on airflow in the human intra-thoracic airways. Respiratory Physiology and Neurobiology 157:295–309
Mandelbrot BB (1982) The Fractal Geometry of Nature. Henry Holt and Company (Macmillan), New York
Weibel ER, Gomez DM (1962) Architecture of the human lung. Use of quantitative methods establishes fundamental relations between size and number of lung structures. Science 137:577–585
Nelson TR, West BJ, Goldberger AL (1990) The fractal lung: universal and species-related scaling patterns. Experientia (Cellular and Molecular Life Sciences) 46:251–254
Mauroy B, Filoche M, Weibel ER, Sapoval B (2004) An optimal bronchial tree may be dangerous. Nature 427:633-636
West BJ, Bhargava V, Goldberger AL (1986) Beyond the principle of similitude: renormalization in the bronchial tree. Journal of Applied Physiology 60:1089–1097
Imre A (1999) Ideas in theoretical biology – Comment about the fractality of the lung. Acta Biotheoretica 47:79–81
Kitaoka H, Takaki R (1999) Fractal analysis of the human fetal lung development. Forma 14:205–212
Hou C, Gheorghiu S, Coppens MO, Huxley VH, Pfeifer P (2005) Gas diffusion through the fractal landscape of the lung: how deep does oxygen enter the alveolar system? (p. 17–30) In: Losa GA, Merlini D, Nonnenmacher TF, Weibel ER (Eds). Fractals in Biology and Medicine, Vol. IV, Birkhäuser, Basel
Hou C, Gheorghiu S, Huxley VH, Pfeifer P (2010) Reverse engineering of oxygen transport in the lung: adaptation to changing demands and resources through space-filling networks. PLoS Computational Biology 6:e1000902
Basset F, Poirier J, Le Crom M, Turiaf J (1971) Ultrastructural study of the human bronchiolar epithelium. Zeitschrift für Zellforschung und mikroskopische Anatomie 116:425–442
Clara M (1937) Zur Histologie des Bronchialepithels Zeitschrift für mikroskopisch-anatomische Forschung 41:321–347
ten Have-Opbroek AA, Otto-Verberne CJ, Dubbeldam JA, Dykman JH (1991) The proximal border of the human respiratory unit, as shown by scanning and transmission electron microscopy and light microscopical cytochemistry. Anatomical Record 229:339–354
Metzger RJ, Krasnow MA (1999) Genetic control of branching morphogenesis. Science 284:1635–1639
Metzger RJ, Klein OD, Martin GR, Krasnow MA (2008) The branching programme of mouse lung development. Nature 453:745–750
Hilfer SR (1996) Morphogenesis of the lung: control of embryonic and fetal branching. Annual Review of Physiology 58:93–113
Jeffery PK (1998) The development of large and small airways. American Journal of Respiratory and Critical Care Medicine 157:S174–S180
Hirashima T, Iwasa Y, Morishita Y (2009) Mechanisms for split localization of Fgf10 expression in early lung development. Developmental Dynamics 238:2813–2822
Thurlbeck WM (1975) Postnatal growth and development of the lung. American Review of Respiratory Diseases 111:803–844
Hislop A, Muir DCF, Jacobsen M, Simon G, Reid L (1972) Postnatal growth and function of the pre-acinar airways. Thorax 27:265–274
Hislop AA, Haworth SG (1989) Airway size and structure in the normal fetal and infant lung and the effect of premature delivery and artificial ventilation. American Review of Respiratory Diseases 140:1717–1726
Horsefield K, Cordon WI, Kemp W, Phillips S (1987) Growth of bronchial tree in man. Thorax 42:383–388
Masters JR (1976) Epithelial-mesenchymal interaction during lung development: the effect of mesenchymal mass. Developmental Biology 51:98–108
Mollard R, Dziadek M (1998) A correlation between epithelial proliferation rates, basement membrane component localization patterns, and morphogenetic potential in the embryonic mouse lung. American Journal of Respiratory Cell and Molecular Biology 19:71–82
Lu P, Werb Z (2008) Patterning mechanisms of branched organs. Science 322:1506–1509
Bellusci S, Grindley J, Emoto H, Itoh N, Hogan BL (1997) Fibroblast growth factor 10 (FGF10) and branching morphogenesis in the embryonic mouse lung. Development 124:4867–4878
Zhou S, Degan S, Potts EN, Foster WM, Sunday ME (2009) NPAS3 is a trachealess homolog critical for lung development and homeostasis. Proceedings of the National Academy of Sciences of the United States of America 106:11691–11696
Serra R, Pelton RW, Moses HL (1994) TGF β1 inhibits branching morphogenesis and N-myc expression in lung bud organ cultures. Development 120:2153–2161
Mahlapuu M, Enerbäck S, Carlsson P (2001) Haploinsufficiency of the forkhead gene Foxf1, a target for sonic hedgehog signaling, causes lung and foregut malformations. Development 128:2397–2406
Li Y, Zhang H, Choi SC, Litingtung Y, Chiang C (2004) Sonic hedgehog signaling regulates Gli3 processing, mesenchymal proliferation, and differentiation during mouse lung organogenesis. Developmental Biology 270:214–231
Motoyama J, Liu J, Mo R, Ding Q, Post M, Hui CC (1998) Essential function of Gli2 and Gli3 in the formation of lung, trachea and oesophagus. Nature – Genetics 20:54–57
Kicheva A, Cohen M, Briscoe J (2012) Developmental pattern formation: insights from physics and biology. Science 338:210–212
Mollard R, Dziadek M (1997) Homeobox genes from clusters A and B demonstrate characteristics of temporal colinearity and differential restrictions in spatial expression domains in the branching mouse lung. International Journal of Developmental Biology 41:655–666
Gjorevski N, Nelson CM (2010) The mechanics of development: models and methods for tissue morphogenesis. Birth Defects Research. Part C, Embryo Today 90:193–202
Schittny JC, Miserocchi G, Sparrow MP (2000) Spontaneous peristaltic airway contractions propel lung liquid through the bronchial tree of intact and fetal lung explants. American Journal of Respiratory Cell and Molecular Biology 23:11–18
Hislop A, Fairweather DV, Blackwell RJ, Howard S (1984) The effect of amniocentesis and drainage of amniotic fluid on lung development in Macaca fascicularis. British Journal of Obstetrics and Gynaecology 91:835–842
Perlman M, Williams J, Hirsch M (1976) Neonatal pulmonary hypoplasia after prolonged leakage of amniotic fluid. Archives of Disease in Childhood 51:349–353
Moore KA, Polte T, Huang S, Shi B, Alsberg E, Sunday ME, Ingber DE (2005) Control of basement membrane remodeling and epithelial branching morphogenesis in embryonic lung by Rho and cytoskeletal tension. Developmental Dynamics 232:268–281
Turing AM (1952) The chemical basis of morphogenesis. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences 237:37–72
Gierer A, Meinhardt H (1972) A theory of biological pattern formation. Kybernetik 12:30–39
Murray JD (2003) On the mechanochemical theory of biological pattern formation with application to vasculogenesis. Comptes Rendues Biologies 326:239–252
Elliott FM, Reid L (1965) Some new facts about the pulmonary artery and its branching pattern. Clinical Radiology 16:193–198
Pump KK (1972) Distribution of bronchial arteries in human lung. Chest 62:447–451
Hislop A, Reid L (1972) Intrapulmonary arterial development during fetal life: branching pattern and structure. Journal of Anatomy 113:35–48
Hislop A, Reid L (1973) Fetal and childhood development of the intrapulmonary veins in man: branching pattern and structure. Thorax 28:313–319
West JB (2008) Respiratory Physiology: The Essentials, Lippincott Williams and Wilkins, Baltimore, MD
Plank L, James J, Wagenvoort CA (1980) Caliber and elastin content of the pulmonary trunk. Archives of Pathology and Laboratory Medicine 104:238–241
Rhoades R, Bell DR (2009) Medical Physiology: Principles for Clinical Medicine, 3rd ed., Wolters Kluwer – Lippincott Williams and Wilkins, Philadelphia, Pennsylvania
Sant’Ambrogio G (1987) Nervous receptors of the tracheobronchial tree. Annual Review of Physiology 49:611–627
Kang S, Jang JH, Price MP, Gautam M, Benson CJ, Gong H, Welsh MJ, Brennan TJ (2012) Simultaneous disruption of mouse ASIC1a, ASIC2 and ASIC3 genes enhances cutaneous mechanosensitivity. PLoS ONE 7:e35225
Manzke T (2005) Expression and function of serotonin receptor isoforms in the respiratory system. PhD Thesis, Göttingen
Heistad DD, Abboud FM, Mark AL, Schmid PG (1974) Interaction of baroreceptor and chemoreceptor reflexes. Modulation of the chemoreceptor reflex by changes in baroreceptor activity. Journal of Clinical Investigation 53:1226–1236
Miura M, Reis DJ (1971) The paramedian reticular nucleus: a site of inhibitory interaction between projections from fastigial nucleus and carotid sinus nerve acting on blood pressure. Journal of Physiology 216:441–460
Miura M, Reis DJ (1972) The role of the solitary and paramedian reticular nuclei in mediating cardiovascular reflex responses from carotid baro- and chemoreceptors. Journal of Physiology 223:525–548
Van De Borne P, Mezzetti S, Montano N, Narkiewicz K, Degaute JP, Somers VK (2000) Hyperventilation alters arterial baroreflex control of heart rate and muscle sympathetic nerve activity. American Journal of Physiology – Heart and Circulatory Physiology 279:H536–H541
Somers VK, Mark AL, Zavala DC, Abboud FM (1989) Influence of ventilation and hypocapnia on sympathetic nerve responses to hypoxia in normal humans. Journal of Applied Physiology 67:2095–2100
Narkiewicz K, van de Borne P, Montano N, Hering D, Kara T, Somers VK (2006) Sympathetic neural outflow and chemoreflex sensitivity are related to spontaneous breathing rate in normal men. Hypertension 47:51–55
Schocken Roth (1977) Reduced β-adrenoceptor concentrations in ageing man. Nature 267:856–858
Barnes P, Jacobs M, Roberts JM (1984) Glucocorticoids preferentially increase fetal alveolar β-adrenoreceptors: autoradiographic evidence. Pediatric Research 18:1191–1194
Schell DN, Durham D, Murphree SS, Muntz KH, Shaul PW (1992) Ontogeny of β-adrenergic receptors in pulmonary arterial smooth muscle, bronchial smooth muscle and alveolar lining cells in the rat. American Journal of Respiratory Cell and Molecular Biology 7:317–324
Puler N, Bernard P, Carrara M, Bencini C, Pacifici GM (1988) Muscarinic cholinergic receptors in lung of developing rats. Developmental Pharmacology and Therapeutics 11:142–146
Sheppard MN, Marangos PJ, Bloom SR, Polak JM (1984) Neuron specific enolase: a marker for the early development of nerves and endocrine cells in the human lung. Life Sciences 34:264–271
Hislop AA, Wharton J, Allen KM, Polak JM, Haworth SG (1990) Immunohistochemical localization of peptide-containing nerves in the airways of normal young children. American Journal of Respiratory Cell and Molecular Biology 3:191–198
Sheppard MN, Polak JM, Allen JM, Bloom SR (1984) Neuropeptide tyrosine (NPY): a newly discovered peptide is present in the mammalian respiratory tract. Thorax 39:326–330
Abdel-Samad D, Perreault C, Ahmarani L, Avedanian L, Bkaily G, Magder S, D’Orlans-Juste P, Jacques D (2012) Differences in neuropeptide Y-induced secretion of endothelin-1 in left and right human endocardial endothelial cells. Neuropeptides pii: S0143–4179(12)00099-6
Allen KM, Wharton J, Polak JM, Haworth SG (1989) A study of nerves containing peptides in the pulmonary vasculature of healthy infants and children and of those with pulmonary hypertension. British Heart Journal 62:353–360
Sharma RK, Addis BJ, Jeffery PK (1995) The distribution and density of airway vasoactive intestinal polypeptide (VIP) binding sites in cystic fibrosis and asthma. Pulmonary Pharmacology 8:91–96
Klabunde RE (2004) Cardiovascular Physiology Concepts. Lippincott Williams and Wilkins, Philadelphia, Pennsylvania (cvphysiology.com)
Kraske S, Cunningham JT, Hajduczok G, Chapleau MW, Abboud FM, Wachtel RE (1998) Mechanosensitive ion channels in putative aortic baroreceptor neurons. American Journal of Physiology – Heart and Circulatory Physiology 275:1497–1501
Krauhs JM (1979) Structure of rat aortic baroreceptors and their relationship to connective tissue. Journal of Neurocytology 8:401–414
Chap. 3. Physiology of the Cardiovascular Apparatus
Bestel J, Clément F, Sorine M (2001) A biomechanical model of muscle contraction (p. 1159–1161). In Niessen WJ, Viergever MA (eds) Medical Image Computing and Computer-Assisted Intervention (MICCAI’01), Lecture Notes in Computer Science (LNCS), vol. 2208, Springer
Krejci P, Sainte-Marie J, Sorine M, Urquiza JM (2006) Solutions to muscle fiber equations and their long time behaviour. Nonlinear Analysis: Real World Applications 7:535558
Sainte-Marie J, Chapelle D, Cimrman R, Sorine M (2006) Modeling and estimation of the cardiac electromechanical activity. Computers and Structures 84:1743–1759
Fernández MA, Gerbeau JF, Grandmont C (2007) A projection semi-implicit scheme for the coupling of an elastic structure with an incompressible fluid. International Journal for Numerical Methods in Engineering 69:794821
Burman E, Fernández MA (2007) Stabilized explicit coupling for fluid–structure interaction using Nitsche’s method. Comptes Rendus de l’Académie des sciences, Paris, Ser. I (Mathematics) 345:467–472
Prassl AJ, Kickinger F, Ahammer H, Grau V, Schneider JE, Hofer E, Vigmond EJ, Trayanova NA, Plank G (2009) Automatically generated, anatomically accurate meshes for cardiac electrophysiology problems. IEEE Transactions on Biomedical Engineering 56:1318–1330
Diniz dos Santos N, Gerbeau JF, Bourgat JF (2008) A partitioned fluid–structure algorithm for elastic thin valves with contact. Computer Methods in Applied Mechanics and Engineering 197:1750–1761
Deng W, Bukiya AN, Rodríguez-Menchaca AA, Zhang Z, Baumgarten CM, Logothetis DE, Levitan I, Rosenhouse-Dantsker A (2012) Hypercholesterolemia induces up-regulation of KACh cardiac currents via a mechanism independent of phosphatidylinositol 4,5-bisphosphate and Gβγ. Journal of Biological Chemistry 287:4925–4935
Moireau P, Chapelle D, Le Tallec P (2008) Joint state and parameter estimation for distributed mechanical systems. Computer Methods in Applied Mechanics and Engineering, 197:659677
Chapelle D, Moireau P, Le Tallec P (2009) Robust filtering for joint state-parameter estimation in distributed mechanical systems. Discrete and Continuous Dynamical Systems, Series A 23:65–84
Poon CS, Merrill CK (1997) Decrease of cardiac chaos in congestive heart failure, Nature 389:492–495
Pironet A, Dauby PC, Paeme S, Kosta S, Chase JG, Desaive T (2013) Simulation of left atrial function using a multi-scale model of the cardiovascular system. PLoS One 8:e65146
Penney D (2003) Cardiac cycle, www.coheadquarters.com/PennLibr/MyPhysiology/
Al-Rubaiee M, Gangula PR, Millis RM, Walker RK, Umoh NA, Cousins VM, Jeffress MA, Haddad GE (2013) Inotropic and lusitropic effects of calcitonin gene-related peptide in the heart. American Journal of Physiology – Heart and Circulatory Physiology 304:H1525–H1537
Robinson TF, Factor SM, Sonnenblick EH (1986) The heart as a suction pump. Scientific American 6:62-69
Pagel PS, Kehl F, Gare M, Hettrick DA, Kersten JR, Warltier DC (2003) Mechanical function of the left atrium: new insights based on analysis of pressure-volume relations and Doppler echocardiography. Anesthesiology 98:975–994
Malik ZA, Kott KS, Poe AJ, Kuo T, Chen L, Ferrara KW, Knowlton AA (2013) Cardiac myocyte exosomes: stability, HSP60, and proteomics. American Journal of Physiology – Heart and Circulatory Physiology 304:H954–H965
Zhang P, Su J, Mende U (2012) Cross talk between cardiac myocytes and fibroblasts: from multiscale investigative approaches to mechanisms and functional consequences. American Journal of Physiology – Heart and Circulatory Physiology 303:H1385–H1396
Sipido KR, Cheng H (2013) T-tubules and ryanodine receptor microdomains: on the road to translation. Cardiovascular Research 98:159–161
Zhang H, Gomez AM, Wang X, Yan Y, Zheng M, Cheng H (2013) ROS regulation of microdomain Ca2+ signalling at the dyads. Cardiovascular Research 98:248–258
Kohl T, Lehnart SE (2013) Imaging T-tubules: dynamic membrane structures for deep functions. Cardiovascular Research 98:162–164
Guo A, Zhang C, Wei S, Chen B, Song LS (2013) Emerging mechanisms of T-tubule remodelling in heart failure. Cardiovascular Research 98:204–215
Shaw RM, Colecraft HM (2013) L-type calcium channel targeting and local signalling in cardiac myocytes. Cardiovascular Research 98:177–186
Scriven DR, Asghari P, Moore ED (2013) Microarchitecture of the dyad. Cardiovascular Research 98:169–176
Tanskanen AJ, Greenstein JL, Chen A, Sun SX, Winslow RL (2007) Protein geometry and placement in the cardiac dyad influence macroscopic properties of calcium-induced calcium release. Biophysical Journal 92:3379–3396
Maier SK, Westenbroek RE, Schenkman KA, Feigl EO, Scheuer T, Catterall WA (2002) An unexpected role for brain-type sodium channels in coupling of cell surface depolarization to contraction in the heart. Proceedings of the National Academy of Sciences of the United States of America 99:4073–4078
Zobel C, Cho HC, Nguyen TT, Pekhletski R, Diaz RJ, Wilson GJ, Backx PH (2003) Molecular dissection of the inward rectifier potassium current (IK1) in rabbit cardiomyocytes: evidence for heteromeric co-assembly of Kir2.1 and Kir2.2. Journal of Physiology 550:365–372
Liu GX, Derst C, Schlichthörl G, Heinen S, Seebohm G, Brüggemann A, Kummer W, Veh RW, Daut J, Preisig-Müller R (2001) Comparison of cloned Kir2 channels with native inward rectifier K+ channels from guinea-pig cardiomyocytes. Journal of Physiology 532:115–126
Gorelik J, Wright PT, Lyon AR, Harding SE (2013) Spatial control of the 0̆3b2AR system in heart failure: the transverse tubule and beyond. Cardiovascular Research 98:216–224
Wu CY, Jia Z, Wang W, Ballou LM, Jiang YP, Chen B, Mathias RT, Cohen IS, Song LS, Entcheva E, Lin RZ (2011) PI3Ks maintain the structural integrity of T-tubules in cardiac myocytes. PLoS One 6:e24404
Chopra N, Knollmann BC (2013) Triadin regulates cardiac muscle couplon structure and microdomain Ca2+ signalling: a path towards ventricular arrhythmias. Cardiovascular Research 98:187–191
Kohlhaas M, Maack C (2013) Calcium release microdomains and mitochondria. Cardiovascular Research 98: 259–268
Plovanich M, Bogorad RL, Sancak Y, Kamer KJ, Strittmatter L, Li AA, Girgis HS, Kuchimanchi S, De Groot J, Speciner L, Taneja N, Oshea J, Koteliansky V, Mootha VK (2013) MICU2, a paralog of MICU1, resides within the mitochondrial uniporter complex to regulate calcium handling. PLoS One 8:e55785
Mallilankaraman K, Cárdenas C, Doonan PJ, Chandramoorthy HC, Irrinki KM, Golenár T, Csordás G, Madireddi P, Yang J, Müller M, Miller R, Kolesar JE, Molgó J, Kaufman B, Hajnóczky G, Foskett JK, Madesh M (2012) MCUR1 is an essential component of mitochondrial Ca2+ uptake that regulates cellular metabolism. Nature – Cell Biology 14:1336–1343
Domenech RJ, Sánchez G, Donoso P, Parra V, Macho P (2003) Effect of tachycardia on myocardial sarcoplasmic reticulum and Ca2+ dynamics: a mechanism for preconditioning? Journal of Molecular and Cellular Cardiology 35:1429–1437
Sánchez G, Pedrozo Z, Domenech RJ, Hidalgo C, Donoso PJ (2005) Tachycardia increases NADPH oxidase activity and RyR2 S-glutathionylation in ventricular muscle. Journal of Molecular and Cellular Cardiology 39:982–991
Beigi F, Gonzalez DR, Minhas KM, Sun QA, Foster MW, Khan SA, Treuer AV, Dulce RA, Harrison RW, Saraiva RM, Premer C, Schulman IH, Stamler JS, Hare JM (2012) Dynamic denitrosylation via S-nitrosoglutathione reductase regulates cardiovascular function. Proceedings of the National Academy of Sciences of the United States of America 109:4314–4319
Lopaschuk GD, Ussher JR, Folmes CD, Jaswal JS, Stanley WC (2010) Myocardial fatty acid metabolism in health and disease. Physiological Reviews 90:207–258
Kahn BB, Alquier T, Carling D, Hardie DG (2005) AMP-activated protein kinase: ancient energy gauge provides clues to modern understanding of metabolism. Cell Metabolism 1: 15–25
Pawlikowska P, Orzechowski A (2007) Role of transmembrane GTPases in mitochondrial morphology and activity [Article in Polish]. Postepy Biochemii 53:53–59
Legros F, Lombès A, Frachon P, Rojo M (2002) Mitochondrial fusion in human cells is efficient, requires the inner membrane potential, and is mediated by mitofusins. Molecular Biology of the Cell 13:4343–4354
Shi Y, Dierckx A, Wanrooij PH, Wanrooij S, Larsson NG, Wilhelmsson LM, Falkenberg M, Gustafsson CM (2012) Mammalian transcription factor A is a core component of the mitochondrial transcription machinery. Proceedings of the National Academy of Sciences of the United States of America 109:16510–16515
Metodiev MD, Lesko N, Park CB, Cámara Y, Shi Y, Wibom R, Hultenby K, Gustafsson CM, Larsson NG (2009) Methylation of 12S rRNA is necessary for in vivo stability of the small subunit of the mammalian mitochondrial ribosome. Cell Metabolism 9:386–397
Spåhr H, Habermann B, Gustafsson CM, Larsson NG, Hallberg BM (2012) Structure of the human MTERF4-NSUN4 protein complex that regulates mitochondrial ribosome biogenesis. Proceedings of the National Academy of Sciences of the United States of America 109:15253–15258
Beck H, Flynn K, Lindenberg KS, Schwarz H, Bradke F, Di Giovanni S, Knöll B (2012) Serum Response Factor (SRF)-cofilin-actin signaling axis modulates mitochondrial dynamics. Proceedings of the National Academy of Sciences of the United States of America 109:E2523-E2532
Murphy MP (2012) Modulating mitochondrial intracellular location as a redox signal. Science Signaling 5:pe39
Carrer M, Liu N, Grueter CE, Williams AH, Frisard MI, Hulver MW, Bassel-Duby R, Olson EN (2012) Control of mitochondrial metabolism and systemic energy homeostasis by microRNAs 378 and 378. Proceedings of the National Academy of Sciences of the United States of America 109:15330–15335
Yu E, Mercer J, Bennett M (2012) Mitochondria in vascular disease. Cardiovascular Research 95:173–182
O’Rourke B (2007) Mitochondrial ion channels. Annual Review of Physiology 69:19–49
O’Rourke B, Cortassa S, Aon MA (2005) Mitochondrial ion channels: gatekeepers of life and death. Physiology 20:303–315
Zaobornyj T, Ghafourifar P (2012) Strategic localization of heart mitochondrial NOS: a review of the evidence. American Journal of Physiology – Heart and Circulatory Physiology 303:H1283–H1293
Virkki LV, Forster IC, Biber J, Murer H (2005) Substrate interactions in the human type IIa sodium-phosphate cotransporter (NaP i -IIa). American Journal of Physiology – Renal Physiology 288:F969–F981
Aprille JR (2003) Mechanism and regulation of the mitochondrial ATP-Mg/P i carrier. Journal of Bioenergetics and Biomembranes 25:473–481
Rich PR (2003) The molecular machinery of Keilin’s respiratory chain. Biochemical Society Transactions 31:1095–1105
Covian R, Balaban RS (2012) Cardiac mitochondrial matrix and respiratory complex protein phosphorylation. American Journal of Physiology – Heart and Circulatory Physiology 303:H940–H966
Illingworth J (Faculty of Biological Sciences, University of Leeds) Bioenergetics, www.bmb.leeds.ac.uk/illingworth/oxphos/index.htm
Lu G, Sun H, Korge P, Koehler CM, Weiss JN, Wang Y (2009) Functional characterization of a mitochondrial Ser/Thr protein phosphatase in cell death regulation. Methods in Enzymology 457:255–273
Castro L, Demicheli V, Tórtora V, Radi R (2011) Mitochondrial protein tyrosine nitration. Free Radical Research 45:37–52
Wirstam M, Blomberg MRA, Siegbahn PEM (1999) Reaction mechanism of compound I formation in heme peroxidases: a density functional theory study. Journal of the American Chemical Society 121:10178–10185
Hurd TR, Costa NJ, Dahm CC, Beer SM, Brown SE, Filipovska A, Murphy MP (2005) Glutathionylation of mitochondrial proteins. Antioxidants and Redox Signaling 7:999–1010
Murphy E, Kohr M, Sun J, Nguyen T, Steenbergen C (2012) S-nitrosylation: a radical way to protect the heart. Journal of Molecular and Cellular Cardiology 52:568–577
Tarze A, Deniaud A, Le Bras M, Maillier E, Molle D, Larochette N, Zamzami N, Jan G, Kroemer G, Brenner C (2007) GAPDH, a novel regulator of the pro-apoptotic mitochondrial membrane permeabilization. Oncogene 26:2606–2620
Sirover MA (2005) New nuclear functions of the glycolytic protein, glyceraldehyde-3-phosphate dehydrogenase, in mammalian cells. Journal of Cellular Biochemistry 95:45–52
Jandu SK, Webb AK, Pak A, Sevinc B, Nyhan D, Belkin AM, Flavahan NA, Berkowitz DE, Santhanam L (2011) Nitric oxide regulates tissue transglutaminase localization and function in the vasculature. Amino Acids 0939-4451:1-9
Gundemir S, Johnson GVW (2009) Intracellular localization and conformational state of transglutaminase 2: implications for cell death. PLoS One 4:e6123
Kim Y, Park J, Kim S, Song S, Kwon SK, Lee SH, Kitada T, Kim JM, Chung J (2008) PINK1 controls mitochondrial localization of Parkin through direct phosphorylation. Biochemical and Biophysical Research Communications 377:975–980
Junn E, Jang WH, Zhao X, Jeong BS, Mouradian MM (2009) Mitochondrial localization of DJ-1 leads to enhanced neuroprotection. Journal of Neuroscience Research 87:123–129
Smirnova E, Griparic L, Shurland DL, van der Bliek AM (2001) Dynamin-related protein Drp1 is required for mitochondrial division in mammalian cells. Molecular Biology of the Cell 12:2245–2256
Schroeder MA, Ali MA, Hulikova A, Supuran CT, Clarke K, Vaughan-Jones RD, Tyler DJ, Swietach P (2013) Extramitochondrial domain rich in carbonic anhydrase activity improves myocardial energetics. Proceedings of the National Academy of Sciences of the United States of America 110:E958–E967
Des Rosiers C, Labarthe F, Lloyd SG, Chatham JC (2011) Cardiac anaplerosis in health and disease: food for thought. Cardiovascular Research 90:210–219
Cotter DG, Schugar RC, Crawford PA (2013) Ketone body metabolism and cardiovascular disease. American Journal of Physiology – Heart and Circulatory Physiology 304:H1060–H1076
Robinson AM, Williamson DH (1978) Utilization of D-3-hydroxy[3–14C]butyrate for lipogenesis in vivo in lactating rat mammary gland. Biochemical Journal 176:635–638
Wise A, Foord SM, Fraser NJ, Barnes AA, Elshourbagy N, Eilert M, Ignar DM, Murdock PR, Steplewski K, Green A, Brown AJ, Dowell SJ, Szekeres PG, Hassall DG, Marshall FH, Wilson S, Pike NB (2003) Molecular identification of high and low affinity receptors for nicotinic acid. Journal of Biological Chemistry 278:9869–9874
Tunaru S, Kero J, Schaub A, Wufka C, Blaukat A, Pfeffer K, Offermanns S (2003) PUMA-G and HM74 are receptors for nicotinic acid and mediate its anti-lipolytic effect. Nature – Medicine 9:352–355
Jeninga EH, Bugge A, Nielsen R, Kersten S, Hamers N, Dani C, Wabitsch M, Berger R, Stunnenberg HG, Mandrup S, Kalkhoven E (2009) Peroxisome proliferator-activated receptor γ regulates expression of the anti-lipolytic G-protein-coupled receptor 81 (GPR81/Gpr81). Journal of Biological Chemistry 284:26385–26393
Irukayama-Tomobe Y, Tanaka H, Yokomizo T, Hashidate-Yoshida T, Yanagisawa M, Sakurai T (2009) Aromatic D-amino acids act as chemoattractant factors for human leukocytes through a G protein-coupled receptor, GPR109B. Proceedings of the National Academy of Sciences of the United States of America 106:3930–3934
Yaniv Y, Spurgeon HA, Ziman BD, Lyashkov AE, Lakatta EG (2013) Mechanisms that match ATP supply to demand in cardiac pacemaker cells during high ATP demand. American Journal of Physiology – Heart and Circulatory Physiology 304:H1428–H1438
Traaseth N, Elfering S, Solien J, Haynes V, Giulivi C (2004) Role of calcium signaling in the activation of mitochondrial nitric oxide synthase and citric acid cycle. Biochimica et Biophysica Acta 1658:64–71
Takahashi E, Asano K (2002) Mitochondrial respiratory control can compensate for intracellular O2 gradients in cardiomyocytes at low PO2. American Journal of Physiology – Heart and Circulatory Physiology 283:H871–H878
Timmer SAJ, Knaapen P (2013) Coronary microvascular function, myocardial metabolism, and energetics in hypertrophic cardiomyopathy: insights from positron emission tomography. European Heart Journal – Cardiovascular Imaging 14:95–101
Chauhan VS, Tuvia S, Buhusi M, Bennett V, Grant AO (2000) Abnormal cardiac Na+ channel properties and QT heart rate adaptation in neonatal ankyrinB knockout mice. Circulation Research 86:441–447
Mohler PJ, Schott JJ, Gramolini AO, Dilly KW, Guatimosim S, duBell WH, Song LS, Haurogne K, Kyndt F, Ali ME, Rogers TB, Lederer WJ, Escande D, Le Marec H, Bennett V (2003) Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death. Nature 421:634–639
Bhasin N, Cunha SR, Mudannayake M, Gigena MS, Rogers TB, Mohler PJ (2007) Molecular basis for PP2A regulatory subunit B56α targeting in cardiomyocytes. American Journal of Physiology – Heart and Circulatory Physiology 293:H109–H119
Marx SO, Kurokawa J, Reiken S, Motoike H, D’Armiento J, Marks AR, Kass RS (2002) Requirement of a macromolecular signaling complex for β adrenergic receptor modulation of the KCNQ1–KCNE1 potassium channel. Science 295:496–499
Wehrens XHT, Lehnart SE, Marks AR (2005) Intracellular calcium release channels and cardiac disease. Annual Review of Physiology 67:69–98
Roberts BN, Yang PC, Behrens SB, Moreno JD, Clancy CE (2012) Computational approaches to understand cardiac electrophysiology and arrhythmias. American Journal of Physiology – Heart and Circulatory Physiology 303:H766–H783
Ha CH, Kim JY, Zhao J, Wang W, Jhun BS, Wong C, Jin ZG (2010) PKA phosphorylates histone deacetylase 5 and prevents its nuclear export, leading to the inhibition of gene transcription and cardiomyocyte hypertrophy. Proceedings of the National Academy of Sciences of the United States of America 107:15467–15472
Hallaq H, Yang Z, Viswanathan PC, Fukuda K, Shen W, Wang DW, Wells KS, Zhou J, Yi J, Murray KT (2006) Quantitation of protein kinase A-mediated trafficking of cardiac sodium channels in living cells. Cardiovascular Research 72:250–261
Rook MB, Evers MM, Vos MA, Bierhuizen MF (2012) Biology of cardiac sodium channel NaV1.5 expression. Cardiovascular Research 93:12–23
Nichols CB, Rossow CF, Navedo MF, Westenbroek RE, Catterall WA, Santana LF, McKnight GS (2010) Sympathetic stimulation of adult cardiomyocytes requires association of AKAP5 with a subpopulation of L-type calcium channels. Circulation Research 107:747–756
Taylor SS, Ilouz R, Zhang P, Kornev AP (2012) Assembly of allosteric macromolecular switches: lessons from PKA. Nature Reviews – Molecular Cell Biology 13:646–658
Aguiar CJ, Andrade VL, Gomes ER, Alves MN, Ladeira MS, Pinheiro AC, Gomes DA, Almeida AP, Goes AM, Resende RR, Guatimosim S, Leite MF (2009) Succinate modulates Ca2+ transient and cardiomyocyte viability through PKA-dependent pathway. Cell Calcium 47:37–46
Houser SR (2009) Ca2+ signaling domains responsible for cardiac hypertrophy and arrhythmias. Circulation Research 104:413–415
Chiang CS, Huang CH, Chieng H, Chang YT, Chang D, Chen JJ, Chen YC, Chen YH, Shin HS, Campbell KP, Chen CC (2009) The CaV3.2 T-type Ca2+ channel is required for pressure overload-induced cardiac hypertrophy in mice. Circulation Research 104:522–530
Terentyev D, Belevych AE, Terentyeva R, Martin MM, Malana GE, Kuhn DE, Abdellatif M, Feldman DS, Elton TS, Györke S (2009) miR-1 overexpression enhances Ca2+ release and promotes cardiac arrhythmogenesis by targeting PP2A regulatory subunit B56alpha and causing CaMKII-dependent hyperphosphorylation of RyR2. Circulation Research 104: 514–521
Carusi A, Burrage K, Rodrguez B (2012) Bridging experiments, models and simulations: an integrative approach to validation in computational cardiac electrophysiology. American Journal of Physiology – Heart and Circulatory Physiology 303:H144–H155
Quinn TA, Kohl P (2013) Combining wet and dry research: experience with model development for cardiac mechano-electric structure-function studies. Cardiovascular Research 97:601–611
Kraeutler MJ, Soltis AR, Saucerman JJ (2010) Modeling cardiac β-adrenergic signaling with normalized-Hill differential equations: comparison with a biochemical model. BMC Systems Biology 4:157
Grandi E, Puglisi JL, Wagner S, Maier LS, Severi S, Bers DM (2007) Simulation of Ca-calmodulin-dependent protein kinase II on rabbit ventricular myocyte ion currents and action potentials. Biophysical Journal 93:3835–3847
Hashambhoy YL, Greenstein JL, Winslow RL (2010) Role of CaMKII in RyR leak, EC coupling and action potential duration: a computational model. Journal of Molecular and Cellular Cardiology 49:617–624
Saucerman JJ, Zhang J, Martin JC, Peng LX, Stenbit AE, Tsien RY, McCulloch AD (2006) Systems analysis of PKA-mediated phosphorylation gradients in live cardiac myocytes. Proceedings of the National Academy of Sciences of the United States of America 103:12923–12928
Iancu RV, Jones SW, Harvey RD (2007) Compartmentation of cAMP signaling in cardiac myocytes: a computational study. Biophysical Journal 92:3317–3331
Himeno Y, Sarai N, Matsuoka S, Noma A (2008) Ionic mechanisms underlying the positive chronotropy induced by beta1-adrenergic stimulation in guinea pig sinoatrial node cells: A simulation study. Journal of Physiological Sciences 58:53–65
Soltis AR, Saucerman JJ (2010) Synergy between CaMKII substrates and β-adrenergic signaling in regulation of cardiac myocyte Ca2+ handling. Biophysical Journal 99:2038–2047
Hodgkin AL and Huxley AF (1952) A quantitative description of membrane current and its application to conduction and excitation in nerve. Journal of Physiology 117:500–544
ten Tusscher KH, Noble D, Noble PJ, Panfilov AV (2004) A model for human ventricular tissue. American Journal of Physiology – Heart and Circulatory Physiology 286:H1573–H1589
Bernus O, Wilders R, Zemlin CW, Verschelde H, Panfilov AV (2002) A computationally efficient electrophysiological model of human ventricular cells. American Journal of Physiology – Heart and Circulatory Physiology 282:H2296–H2308
Beeler GW, Reuter H (1977) Reconstruction of the action potential of ventricular myocardial fibres. Journal of Physiology 268:177-210
Mitchell CC, Schaeffer DG (2003) A two-current model for the dynamics of cardiac membrane. Bulletin of Mathematical Biology 65:767–793
Aliev RR, Panfilov AV (1996) A simple two-variable model of cardiac excitation. Chaos Solitons Fractals 7:293–301
Fenton F, Karma A (1998) Vortex dynamics in three-dimensional continuous myocardium with fiber rotation: Filament instability and fibrillation. Chaos 8:20-47
Luo CH, Rudy Y (1991) A model of the ventricular cardiac action-potential: depolarization, repolarization, and their interaction. Circulation Research 68:1501–1526
Djabella K, Sorine M. (2006) A reduced differential model for cardiac action potentials. SIAM Conference on the Life Sciences, Raleigh, USA
Tolkacheva EG, Schaeffer DG, Gauthier DJ, Mitchell CC (2002) Analysis of the Fenton-Karma model through an approximation by a one-dimensional map. Chaos 12:1034–1042
Boulakia M, Cazeau S, Fernndez MA, Gerbeau JF, Zemzemi N (2010) Mathematical modeling of electrocardiograms: a numerical study. Annals of Biomedical Engineering 38:1071–1097
Jiao Q, Bai Y, Akaike T, Takeshima H, Ishikawa Y, Minamisawa S (2009) Sarcalumenin is essential for maintaining cardiac function during endurance exercise training. American Journal of Physiology – Heart and Circulatory Physiology 297:H576–H582
Guyton AC, Hall JE (2006) Textbook of medical physiology (7th Edition) Elsevier – Saunders, Philadelphia, Pennsylvania
Milnor WR (1982) Haemodynamics. Williams and Wilkins, Baltimore, MD
Silbernagl S, Despopoulos A (2001) Atlas de poche de physiologie [Pocket Atlas of Physiology]. Flammarion, Paris
Davies JI, Struthers AD (2003) Pulse wave analysis and pulse wave velocity: a critical review of their strengths and weaknesses. Journal of Hypertension 21:463–472
Meaney, E, Alva F, Moguel R, Meaney A, Alva J, Webel R (2000) Formula and nomogram for the sphygmomanometric calculation of the mean arterial pressure. Heart 84:64
Learoyd BM, Taylor MG (1996) Alterations with age in the viscoelastic properties of human arterial walls. Circulation Research 18:278–292
Mills CJ, Gabe IT, Gault JH, Mason DT, Ross J Jr, Braunwald E, Shillingford JP (1970) Pressure-flow relationships and vascular impedance in man. Cardiovascular Research 4: 405–417
Anliker M et al (1977) Non-invasive measurement of blood flow, In: Hwang NHC, Normann NA (eds) Cardiovascular flow dynamics and measurements. University Park Press, Baltimore
Bergfeld GR, Forrester T (1992) Release of ATP from human erythrocytes in response to a brief period of hypoxia and hypercapnia. Cardiovascular Research 26:40–47
McCullough WT, Collins DM, Ellsworth ML (1997) Arteriolar responses to extracellular ATP in striated muscle. American Journal of Physiology – Heart and Circulatory Physiology 272:H1886–H1891
Arciero JC, Carlson BE, Secomb TW (2008) Theoretical model of metabolic blood flow regulation: roles of ATP release by red blood cells and conducted responses. American Journal of Physiology – Heart and Circulatory Physiology 295:H1562–H1571
Kalmanson D, Veyrat C (1978) Clinical aspects of venous return: a velocimetric approach to a new system dynamics concept. In: Baan J, Noordegraaf A, Raines J (eds) Cardiovascular System Dynamics. MIT Press, Cambridge
Moreno AH (1978) Dynamics of pressure in the central veins. In: Baan J, Noordegraaf A, Raines J (eds) Cardiovascular System Dynamics. MIT Press, Cambridge
Hoffman JI, Spaan JA (1990) Pressure-flow relations in coronary circulation. Physiological Reviews 70:331–390
Shukla P, Sun C, O’Rourke ST (2012) Melatonin inhibits nitric oxide signaling by increasing PDE5 phosphorylation in coronary arteries. American Journal of Physiology – Heart and Circulatory Physiology 303:H1418–H1425
Scaramucci J (1695) De motu cordis, theorema sexton. Theoremata familiaria viros eruditos consulentia de variis physico medicis lucubrationibus iucta leges mecanicas. Urbino, Italy: Apud Joannem Baptistam Bustum, 70–81
Lenègre J, Blondeau M; Bourdarias JP, Gerbaux A, Himbert J, Maurice P (1973) Cœur et Circulation [Heart and Circulation]. In Vallery-Radot P, Hamburger J, Lhermitte F (eds) Pathologie Mdicale. [Medical Pathology] (Vol.3), Flammarion Mdecine Sciences, Paris
Mori H, Tanaka E, Hyodo K, Mohammed MU, Sekka T, Ito K, Shinozaki Y, Tanaka A, Nakazawa H, Abe S, Handa S, Kubota M, Tanioka K, Umetani K, Ando M (1999) Synchrotron microangiography reveals configurational changes and to-and-fro flow in intramyocardial vessels. American Journal of Physiology. Heart Circulation Physiology 276:H429–H437
Carlson BE, Arciero JC, Secomb TW (2008) Theoretical model of blood flow autoregulation: roles of myogenic, shear-dependent, and metabolic responses. American Journal of Physiology – Heart and Circulatory Physiology 295:H1572–H1579
Olsson RA (1981) Local factors regulating cardiac and skeletal muscle blood flow. Annual Review of Physiology 43:385–395
Momen A, Mascarenhas V, Gahremanpour A, Gao Z, Moradkhan R, Kunselman A, Boehmer JP, Sinoway LI, Leuenberger UA (2009) Coronary blood flow responses to physiological stress in humans. American Journal of Physiology – Heart and Circulatory Physiology 296:H854–H861
Caesar K, Offenhauser N, Lauritzen M (2008) Gamma-aminobutyric acid modulates local brain oxygen consumption and blood flow in rat cerebellar cortex. Journal of Cerebral Blood Flow and Metabolism 28:906–915
Stefanovic B, Hutchinson E, Yakovleva V, Schram V, Russell JT, Belluscio L, Koretsky AP, Silva AC (2008) Functional reactivity of cerebral capillaries. Journal of Cerebral Blood Flow and Metabolism 28:961–972
Sirotin YB, Das A (2009) Anticipatory haemodynamic signals in sensory cortex not predicted by local neuronal activity. Nature 457:475–479
van Beek AHEA, Claassen JAHR, Rikkert MGMO, Jansen RWMM (2008) Cerebral autoregulation: an overview of current concepts and methodology with special focus on the elderly. Journal of Cerebral Blood Flow and Metabolism 28:1071–1085
Tzeng YC, Ainslie PN, Cooke WH, Peebles KC, Willie CK, Macrae BA, Smirl JD, Horsman HM, Rickards CA (2012) Assessment of cerebral autoregulation: the quandary of quantification. American Journal of Physiology – Heart and Circulatory Physiology 303:H658–H671
Fonck E, Feigl GG, Fasel J, Sage D, Unser M, Rüfenacht DA, Stergiopulos N (2009) Effect of aging on elastin functionality in human cerebral arteries. Stroke 40:2552–2556
West JB (1974) Respiratory Physiology. Williams and Wilkins, Baltimore, MD
Wagner WW, Latham LP (1975) Pulmonary capillary recruitment during airway hypoxia in the dog. Journal of Applied Physiology 39:900–905
Hanson WL, Emhardt JD, Bartek JP, Latham LP, Checkley LL, Capen RL, Wagner WW (1989) Site of recruitment in the pulmonary microcirculation. Journal of Applied Physiology 66:2079–2083
Dawson CA, Rickaby DA, Linehan JH (1986) Location and mechanisms of pulmonary vascular volume changes. Journal of Applied Physiology 60:402–409
Barman SA, Taylor AE (1990) Effect of pulmonary venous pressure elevation on vascular resistance and compliance. American Journal of Physiology – Heart and Circulatory Physiology 258:H1164–H1170
Ryan JW, Ryan US, Schultz DR, Whitaker C, Chung A (1975) Subcellular localization of pulmonary antiotensin-converting enzyme (kininase II). Biochemical Journal 146:497–499
Curry FRE, Adamson RH (2010) Vascular permeability modulation at the cell, microvessel, or whole organ level: towards closing gaps in our knowledge. Cardiovascular Research 87:218–229
Perktold K, Prosi M, Zunino P (2009) Mathematical models of mass transfer in the vascular walls (Chap. 7). In Formaggia L, Quarteroni A, Veneziani A (eds.) Cardiovascular Mathematics: Modeling and Simulation of the Circulatory System, Springer, Milano
Shen Q, Rigor RR, Pivetti CD, Wu MH, Yuan SY (2010) Myosin light chain kinase in microvascular endothelial barrier function. Cardiovascular Research 87:272–280
Curry FRE, Noll T (2010) Spotlight on microvascular permeability. Cardiovascular Research 87:195–197
VanTeeffelen JWGE, Brands J, Vink H (2010) Agonist-induced impairment of glycocalyx exclusion properties: contribution to coronary effects of adenosine. Cardiovascular Research 87:311–319
Spindler V, Schlegel1 N, Waschke1 J (2010) Role of GTPases in control of microvascular permeability. Cardiovascular Research 87:243–253
Durán WN, Breslin JW, Sánchez FA (2010) The NO cascade, eNOS location, and microvascular permeability. Cardiovascular Research 87:254–261
Bates DO (2010) Vascular endothelial growth factors and vascular permeability. Cardiovascular Research 87:262–271
Zhou X, He P (2010) Endothelial [Ca2+]i and caveolin-1 antagonistically regulate eNOS activity and microvessel permeability in rat venules. Cardiovascular Research 87:340–347
Rabiet M-J, Plantier J-L, Rival Y, Genoux Y, Lampugnani MG, Dejana E (1996) Thrombin-induced increase in endothelial permeability is associated with changes in cell-to-cell junction organization. Arteriosclerosis, Thrombosis, and Vascular Biology 16:488–496
Sun C, Wu MH, Guo M, Day ML, Lee ES, Yuan SY (2010) ADAM15 regulates endothelial permeability and neutrophil migration via Src/ERK1/2 signalling. Cardiovascular Research 87:348–355
He P (2010) Leucocyte/endothelium interactions and microvessel permeability: coupled or uncoupled? Cardiovascular Research 87:281–290
Ngok SP, Geyer R, Liu M, Kourtidis A, Agrawal S, Wu C, Seerapu HR, Lewis-Tuffin LJ, Moodie KL, Huveldt D, Marx R, Baraban JM, Storz P, Horowitz A, Anastasiadis PZ (2012) VEGF and Angiopoietin-1 exert opposing effects on cell junctions by regulating the Rho GEF Syx. Journal of Cell Biology 199:1103–1115
Michel CC, Curry FE (1999) Microvascular permeability. Physiological Reviews 79:703–761
Weinbaum S, Curry FE (1995) Modelling the structural pathways for transcapillary exchange. Symposia of the Society for Experimental Biology 49:323–345
Agre P, Brown D, Nielsen S (1995) Aquaporin water channels: unanswered questions and unresolved controversies. Current Opinion in Cell Biology 7:472–483
Tarbell JM, Demaio L, Zaw MM (1999) Effect of pressure on hydraulic conductivity of endothelial monolayers: role of endothelial cleft shear stress. Journal of Applied Physiology 87:261–268
Chen SC, Liu KM, Wagner RC (1998) Three-dimensional analysis of vacuoles and surface invaginations of capillary endothelia in the eel rete mirabile. Anatomical Record 252:546–553
Tarbell JM (2010) Shear stress and the endothelial transport barrier. Cardiovascular Research 87:320–330
Reed RK, Rubin K (2010) Transcapillary exchange: role and importance of the interstitial fluid pressure and the extracellular matrix. Cardiovascular Research 87:211–217
Levick JR, Michel CC (2010) Microvascular fluid exchange and the revised Starling principle. Cardiovascular Research 87:198–210
Minami Y, Kasukawa T, Kakazu Y, Iigo M, Sugimoto M, Ikeda S, Yasui A, van der Horst GT, Soga T, Ueda HR (2009) Measurement of internal body time by blood metabolomics. Proceedings of the National Academy of Sciences of the United States of America 106:9890–9895
Curtis AM, Cheng Y, Kapoor S, Reilly D, Price TS, FitzGerald GA (2007) Circadian variation of blood pressure and the vascular response to asynchronous stress. Proceedings of the National Academy of Sciences of the United States of America 104:3450–3455
Fuller PM, Lu J, Saper CB (2008) Differential rescue of light- and food-entrainable circadian rhythms. Science 320:1074–1077
Davidson AJ, London B, Block GD, Menaker M (2005) Cardiovascular tissues contain independent circadian clocks. Clinical and Experimental Hypertension 27:307–311
McNamara P, Seo SP, Rudic RD, Sehgal A, Chakravarti D, FitzGerald GA (2001) Regulation of CLOCK and MOP4 by nuclear hormone receptors in the vasculature: a humoral mechanism to reset a peripheral clock. Cell 105:877–889
Damiola F, Le Minh N, Preitner N, Kornmann B, Fleury-Olela F, Schibler U (2000) Restricted feeding uncouples circadian oscillators in peripheral tissues from the central pacemaker in the suprachiasmatic nucleus. Genes and Development 14:2950–2961
Balsalobre A, Brown SA, Marcacci L, Tronche F, Kellendonk C, Reichardt HM, Schutz G, Schibler U (2000) Resetting of circadian time in peripheral tissues by glucocorticoid signaling. Science 289:2344–2347
Lemmer B (1992) Cardiovascular chronobiology and chronopharmacology. In: Touitou Y, Haus E (eds) Biologic Rhythms in Clinical and Laboratory Medicine, 418–427. Springer-Verlag, Berlin.
Bray MS, Young ME (2008) Diurnal variations in myocardial metabolism. Cardiovascular Research 79:228–237
Martino TA, Oudit GY, Herzenberg AM, Tata N, Koletar MM, Kabir GM, Belsham DD, Backx PH, Ralph MR, Sole MJ (2008) Circadian rhythm disorganization produces profound cardiovascular and renal disease in hamsters. American Journal of Physiology – Regulatory, Integrative and Comparative Physiology 294:R1675–1683
Ivanov PC, Hu K, Hilton MF, Shea SA, Stanley HE (2007) Endogenous circadian rhythm in human motor activity uncoupled from circadian influences on cardiac dynamics. Proceedings of the National Academy of Sciences of the United States of America 104:20702–20707
Pennes HH (1948) Analysis of tissue and arterial blood temperatures in the resting human forearm. Journal of Applied Physiology 1:93–122
Valvano JW, Bioheat transfer. users.ece.utexas.edu/ ∼ valvano/research/jwv.pdf
Werner J, Brinck H (2001) A three-dimensional vascular model and its application to the determination of the spatial variations in the arterial, venous, and tissue temperature distribution, In: Leondes C (ed) Biofluid Methods in Vascular and Pulmonary Systems. CRC Press, Boca Raton, FL
Wissler EH (1998) Pennes’ 1948 paper revisited. Journal of Applied Physiology 85:35–41
Arkin H, Xu LX, Holmes KR (1994) Recent developments in modeling heat transfer in blood perfused tissues. IEEE Transactions on Biomedical Engineering 41:97–107
Tedgui A, Lvy B (1994) Biologie de la paroi artrielle [Biology of the Arterial Wall]. Masson, Paris
Dongaonkar RM, Nguyen TL, Quick CM, Hardy J, Laine GA, Wilson E, Stewart RH (2013) Adaptation of mesenteric lymphatic vessels to prolonged changes in transmural pressure. American Journal of Physiology – Heart and Circulatory Physiology 305:H203–H210
Bayliss W (1902) On the local reactions of the arterial wall to changes of internal pressure. Journal of Physiology 28:220–231
Davis MJ (2012) Perspective: physiological role(s) of the vascular myogenic response. Microcirculation 19:99-114
Lidington D, Schubert R, Bolz SS (2013) Capitalizing on diversity: an integrative approach towards the multiplicity of cellular mechanisms underlying myogenic responsiveness. Cardiovascular Research 97:404–412
Storch U, Schnitzler MM, Gudermann T (2012) G protein-mediated stretch reception. American Journal of Physiology – Heart and Circulatory Physiology 302:H1241–H1249
Pluznick JL, Protzko RJ, Gevorgyan H, Peterlin Z, Sipos A, Han J, Brunet I, Wan LX, Rey F, Wang T, Firestein SJ, Yanagisawa M, Gordon JI, Eichmann A, Peti-Peterdi J, Caplan MJ (2013) Olfactory receptor responding to gut microbiota-derived signals plays a role in renin secretion and blood pressure regulation. Proceedings of the National Academy of Sciences of the United States of America 110:4410–4415
Inoue R, Jian Z, Kawarabayashi Y (2009) Mechanosensitive TRP channels in cardiovascular pathophysiology. Pharmacology and Therapeutics 123:371–385
Yin J, Kuebler WM (2010) Mechanotransduction by TRP channels: general concepts and specific role in the vasculature. Cell Biochemistry and Biophysics 56:1–18
Baumgarten CM (2007) Origin of Mechanotransduction: Stretch-Activated Ion Channels (Chap. 2) In Weckstrom M, Tavi P (eds.) Cardiac Mechanotransduction. Landes Bioscience, Austin, Texas, and Springer, New York
Coste B, Xiao B, Santos JS, Syeda R, Grandl J, Spencer KS, Kim SE, Schmidt M, Mathur J, Dubin AE, Montal M, Patapoutian A (2012) Piezo proteins are pore-forming subunits of mechanically activated channels. Nature 483:176–181
Hill MA, Trippe KM, Li QX, Meininger GA (1992) Arteriolar arcades and pressure distribution in cremaster muscle microcirculation. Microvascular Research 44:117–124
Chlopicki S, Nilsson H, Mulvany MJ (2001) Initial and sustained phases of myogenic response of rat mesenteric small arteries. American Journal of Physiology – Heart and Circulatory Physiology 281:H2176–H2183
Zou H, Ratz PH, Hill MA (2000) Temporal aspects of Ca2+ and myosin phosphorylation during myogenic and norepinephrine-induced arteriolar constriction. Journal of Vascular Research 37:556–567
Bolz SS, Vogel L, Sollinger D, Derwand R, Boer C, Pitson SM, Spiegel S, and Pohl U (2003) Sphingosine kinase modulates microvascular tone and myogenic responses through activation of RhoA/Rho kinase. Circulation 108:342–347
Yeon DS, Kim JS, Ahn DS, Kwon SC, Kang BS, Morgan KG, Lee YH (2002) Role of protein kinase C- or RhoA-induced Ca2+ sensitization in stretch-induced myogenic tone. Cardiovascular Research 53:431–438
Frisbee JC, Roman RJ, Krishna UM, Falck JR, Lombard JH (2001) 20-HETE modulates myogenic response of skeletal muscle resistance arteries from hypertensive Dahl-SS rats. American Journal of Physiology – Heart and Circulatory Physiology 280:H1066–H1074
Obara K, Koide M, Nakayama K (2002) 20-Hydroxyeicosatetraenoic acid potentiates stretch-induced contraction of canine basilar artery via PKC alpha-mediated inhibition of KCa channel. British Journal of Pharmacology 137:1362–1370
Martinez-Lemus LA, Wu X, Wilson E, Hill MA, Davis GE, Davis MJ, Meininger GA (2003) Integrins as unique receptors for vascular control. Journal of Vascular Research 40:211–233
Sun Z, Martinez-Lemus LA, Trache A, Trzeciakowski JP, Davis GE, Pohl U, Meininger GA (2005) Mechanical properties of the interaction between fibronectin and α5β1-integrin on vascular smooth muscle cells studied using atomic force microscopy. American Journal of Physiology – Heart and Circulatory Physiology 289:H2526–H2535
Martinez-Lemus LA, Crow T, Davis MJ, Meininger GA (2005) αVβ3- and α5β1-integrin blockade inhibits myogenic constriction of skeletal muscle resistance arterioles. American Journal of Physiology – Heart and Circulatory Physiology 289:H322–H329
Hong Z, Sun Z, Li Z, Mesquitta WT, Trzeciakowski JP, Meininger GA (2012) Coordination of fibronectin adhesion with contraction and relaxation in microvascular smooth muscle. Cardiovascular Research 96:73–80
Schmid-Schönbein GW (2012) The integrin–cortex complex under control of GPCRs. Cardiovascular Research 96:7–8
Nelson MT, Cheng H, Rubart M, Santana LF, Bonev AD, Knot HJ, Lederer WJ (1995) Relaxation of arterial smooth muscle by calcium sparks. Science 270:633–637
Bagher P, Beleznai T, Kansui Y, Mitchell R, Garland CJ, Dora KA (2012) Low intravascular pressure activates endothelial cell TRPV4 channels, local Ca2+ events, and IKCa channels, reducing arteriolar tone. Proceedings of the National Academy of Sciences of the United States of America 109:18174–18179
Harder DR, Roman RJ, Gebremedhin D, Birks EK, Lange AR (1998) A common pathway for regulation of nutritive blood flow to the brain: arterial muscle membrane potential and cytochrome P450 metabolites. Acta Physiologica Scandinavica 164:527–532
Fischell TA, Bausback KN, McDonald TV (1990) Evidence for altered epicardial coronary artery autoregulation as a cause of distal coronary vasoconstriction after successful percutaneous transluminal coronary angioplasty. Journal of Clinical Investigation 86:575–584
Davis MJ, Hill MA (1999) Signaling mechanisms underlying the vascular myogenic response. Physiological Reviews 79:387–423
Mederos y Schnitzler M, Storch U, Meibers S, Nurwakagari P, Breit A, Essin K, Gollasch M, Gudermann T (2008) Gq-coupled receptors as mechanosensors mediating myogenic vasoconstriction. EMBO Journal 27:3092–3103
Zou Y, Akazawa H, Qin Y, Sano M, Takano H, Minamino T, Makita N, Iwanaga K, Zhu W, Kudoh S, Toko H, Tamura K, Kihara M, Nagai T, Fukamizu A, Umemura S, Iiri T, Fujita T, Komuro I (2004) Mechanical stress activates angiotensin II type 1 receptor without the involvement of angiotensin II. Nature – Cell Biology 6:499–506
Hofmann T, Obukhov AG, Schaefer M, Harteneck C, Gudermann T, Schultz G (1999) Direct activation of human TRPC6 and TRPC3 channels by diacylglycerol. Nature 397:259–263
Nilius B, Owsianik G, Voets T, Peters JA (2007) Transient receptor potential cation channels in disease. Physiological Reviews 87:165–217
Sriram K, Salazar Vázquez BY, Tsai AG, Cabrales P, Intaglietta M, Tartakovsky DM (2012) Autoregulation and mechanotransduction control the arteriolar response to small changes in hematocrit. American Journal of Physiology – Heart and Circulatory Physiology 303:H1096–H1106
Chu C, Thai K, Park KW, Wang P, Makwana O, Lovett DH, Simpson PC, Baker AJ (2013) Intraventricular and interventricular cellular heterogeneity of inotropic responses to α1-adrenergic stimulation. American Journal of Physiology – Heart and Circulatory Physiology 304:H946–H953
Guyenet PG (2006) The sympathetic control of blood pressure. Nature Reviews – Neuroscience 7:335–346
Pyke KE, Poitras V, Tschakovsky ME (2008) Brachial artery flow-mediated dilation during handgrip exercise: evidence for endothelial transduction of the mean shear stimulus. American Journal of Physiology – Heart and Circulatory Physiology 294:H2669–H2679
Green DJ, Bilsborough W, Naylor LH, Reed C, Wright J, O’Driscoll G, Walsh JH (2005) Comparison of forearm blood flow responses to incremental handgrip and cycle ergometer exercise: relative contribution of nitric oxide. Journal of Physiology 562:617–628
Guo ZL, Tjen-A-Looi SC, Fu LW, Longhurst JC (2009) Nitric oxide in rostral ventrolateral medulla regulates cardiac-sympathetic reflexes: role of synthase isoforms. American Journal of Physiology – Heart and Circulatory Physiology 297:H1478–H1486
Izumi H, Karita K (1994) The parasympathetic vasodilator fibers in the trigeminal portion of the distal lingual nerve in the cat tongue. American Journal of Physiology 266:R1517–R1522
Oakley AE, Clifton DK, Steiner RA (2009) Kisspeptin signaling in the brain. Endocrine Reviews 30:713–743
Rometo AM, Rance NE (2008) Changes in prodynorphin gene expression and neuronal morphology in the hypothalamus of postmenopausal women. Journal of Neuroendocrinology 20:1376–1381
Mittelman-Smith MA, Williams H, Krajewski-Hall SJ, McMullen NT, Rance NE (2012) Role for kisspeptin/neurokinin B/dynorphin (KNDy) neurons in cutaneous vasodilatation and the estrogen modulation of body temperature. Proceedings of the National Academy of Sciences of the United States of America 109:19846–19851
Ieda M, Kanazawa H, Kimura K, Hattori F, Ieda Y, Taniguchi M, Lee JK, Matsumura K, Tomita Y, Miyoshi S, Shimoda K, Makino S, Sano M, Kodama I, Ogawa S, Fukuda K (2007) Sema3a maintains normal heart rhythm through sympathetic innervation patterning. Nature – Medicine 13:604–612
Fu LW, Guo ZL, Longhurst JC (2012) Ionotropic glutamate receptors in the external lateral parabrachial nucleus participate in processing cardiac sympathoexcitatory reflexes. American Journal of Physiology – Heart and Circulatory Physiology 302:H1444–H1453
Koba S, Gao Z, Xing J, Sinoway LI, Li J (2006) Sympathetic responses to exercise in myocardial infarction rats: a role of central command. American Journal of Physiology – Heart and Circulatory Physiology 291, H2735-H2742
Sin PY, Galletly DC, Tzeng YC (2010) Influence of breathing frequency on the pattern of respiratory sinus arrhythmia and blood pressure: old questions revisited. American Journal of Physiology – Heart and Circulatory Physiology 298:H1588–H1599
Blain G, Meste O, Blain A, Bermon S (2009) Time-frequency analysis of heart rate variability reveals cardiolocomotor coupling during dynamic cycling exercise in humans. American Journal of Physiology-Heart and Circulatory Physiology 296:H1651-H1659
Aletti F, Bassani T, Lucini D, Pagani M, Baselli G (2009) Multivariate decomposition of arterial blood pressure variability for the assessment of arterial control of circulation. IEEE Transactions on Biomedical Engineering 56:1781–1790
Kamiya A, Kawada T, Mizuno M, Shimizu S, Sugimachi M (2010) Parallel resetting of arterial baroreflex control of renal and cardiac sympathetic nerve activities during upright tilt in rabbits. American Journal of Physiology – Heart and Circulatory Physiology 298:H1966–H1975
Tigerstedt R, Bergman P (1898) Niere und Kreislauf [Kidney and circulation]. Skandinavisches Archiv für Physiologie 8:223–271
James PF, Grupp IL, Grupp G, Woo AL, Askew GR, Croyle ML, Walsh RA, Lingrel JB (1999) Identification of a specific role for the Na, K-ATPase α2 isoform as a regulator of calcium in the heart. Molecular Cell 3:555–563
Blaustein MP, Leenen FH, Chen L, Golovina VA, Hamlyn JM, Pallone TL, Van Huysse JW, Zhang J, Wier WG (2012) How NaCl raises blood pressure: a new paradigm for the pathogenesis of salt-dependent hypertension. American Journal of Physiology – Heart and Circulatory Physiology 302:H1031–H1049
Gao J, Wymore RS, Wang Y, Gaudette GR, Krukenkamp IB, Cohen IS, Mathias RT (2002) Isoform-specific stimulation of cardiac Na/K pumps by nanomolar concentrations of glycosides. Journal of General Physiology 119:297–312
Crowley SD, Gurley SB, Herrera MJ, Ruiz P, Griffiths R, Kumar AP, Kim HS, Smithies O, Le TH, Coffman TM (2006) Angiotensin II causes hypertension and cardiac hypertrophy through its receptors in the kidney. Proceedings of the National Academy of Sciences of the United States of America 103:17985–17990
Machnik A, Neuhofer W, Jantsch J, Dahlmann A, Tammela T, Machura K, Park JK, Beck FX, Müller DN, Derer W, Goss J, Ziomber A, Dietsch P, Wagner H, van Rooijen N, Kurtz A, Hilgers KF, Alitalo K, Eckardt KU, Luft FC, Kerjaschki D, Titze J (2009) Macrophages regulate salt-dependent volume and blood pressure by a vascular endothelial growth factor-C-dependent buffering mechanism. Nature – Medicine 15:545–552
Smith OA, Astley CA, Spelman FA, Golanov EV, Bowden DM, Chesney MA, Chalyan V (2000) Cardiovascular responses in anticipation of changes in posture and locomotion. Brain Research Bulletin 53:69–76
Taylor JA, Eckberg DL (1996) Fundamental relations between short-term RR interval and arterial pressure oscillations in humans. Circulation 93:1527–1532
Zhang R, Khoo MSC, Wu Y, Yang Y, Grueter CE, Ni G, Price EE, Thiel W, Guatimosim S, Song LS, Madu EC, Shah AN, Vishnivetskaya TA, Atkinson JB, Gurevich VV, Salama G, Lederer WJ, Colbran RJ, Anderson ME (2005) Calmodulin kinase II inhibition protects against structural heart disease. Nature – Medicine 11:409–417
Goyal RK (1989) Muscarinic receptor subtypes: physiology and clinical implications. New England Journal of Medicine 321:1022–1029
Lymperopoulos A, Rengo G, Funakoshi H, Eckhart AE, Koch WJ (2007) Adrenal GRK2 upregulation mediates sympathetic overdrive in heart failure. Nature – Medicine 13:315–323
Monti A, Mdigue C, Sorine M (2002) Short-term modelling of the controlled cardiovascular system. ESAIM: Proceedings 12:115–128
Hammer PE, Saul JP (2005) Resonance in a mathematical model of baroreflex control: arterial blood pressure waves accompanying postural stress. American Journal of Physiology – Regulatory, Integrative and Comparative Physiology 288:R1637–R1648.
Degtyarenko AM, Kaufman MP (2005) MLR-induced inhibition of barosensory cells in the NTS. American Journal of Physiology – Heart and Circulatory Physiology 289:H2575–H2584
Ulrich-Lai1 YM, Herman JP (2009) Neural regulation of endocrine and autonomic stress responses. Nature Reviews – Neuroscience 10:397–409
Joëls M, Baram TZ (2009) The neuro-symphony of stress. Nature Reviews – Neuroscience 10:459–466
Watts SW, Morrison SF, Davis RP, Barman SM (2012) Serotonin and blood pressure regulation. Pharmacological Reviews 64:359–388
Ramage AG, Villalón CM (2008) 5-hydroxytryptamine and cardiovascular regulation. Trends in Pharmacological Sciences 29:472–481
Kurbel S, Dodig K, Radic R (2002) The osmotic gradient in kidney medulla: a retold story. Advances in Physiology Education 26:278–281
Lombes M, Farman N, Oblin ME, Baulieu EE, Bonvalet JP, Erlanger BF, Gasc J (1990) Immunohistochemical localization of renal mineralocorticoid receptor by using an anti-idiotypic antibody that is an internal image of aldosterone. Proceedings of the National Academy of Sciences of the United States of America 87:1086–1088
Sasano H, Fukushima K, Sasaki I, Matsuno S, Nagura H, Krozowski ZS (1992) Immunolocalization of mineralocorticoid receptor in human kidney, pancreas, salivary, mammary and sweat glands: a light and electron microscopic immunohistochemical study. Journal of Endocrinology 132:305–310
Cantin M, Genest J (1986) Le cœur est une glande endocrine [The heart is an endocrine gland]. Pour la Science 102:43–49
Kondoh G, Tojo H, Nakatani N, N Komazawa, Murata C, Yamagata K, Maeda Y, Kinoshita T, Okabe M, Taguchi R, Takeda J (2005) Angiotensin-converting enzyme is a GPI-anchored protein releasing factor crucial for fertilization. Nature – Medicine 11:160–166
Lalioti MD, Zhang J, Volkman HM, Kahle KT, Hoffmann KE, Toka HR, Nelson-Williams C, Ellison DE, Flavell R, Booth CJ, Lu Y, Geller DS, Lifton RP (2006) Wnk4 controls blood pressure and potassium homeostasis via regulation of mass and activity of the distal convoluted tubule. Nature – Genetics 38:1124–1132
Coffman TM (2006) A WNK in the kidney controls blood pressure. Nature – Genetics 38:1105–1106
Jentsch TJ, Hbner CA, Fuhrmann JC (2004) Ion channels: Function unravelled by dysfunction. Nature – Cell Biology 6:1039–1047 (2004)
Oberleithner H, Riethmller C, Schillers H, MacGregor GH, de Wardener HE, Hausberg M (2007) Plasma sodium stiffens vascular endothelium and reduces nitric oxide release. Proceedings of the National Academy of Sciences of the United States of America 104:16281–16286
de Kloet AD, Krause EG, Scott KA, Foster MT, Herman JP, Sakai RR, Seeley RJ, Woods SC (2011) Central angiotensin II has catabolic action at white and brown adipose tissue. American Journal of Physiology – Endocrinology and Metabolism 301:E1081–E1091
Yoshida T, Semprun-Prieto L, Wainford RD, Sukhanov S, Kapusta DR, Delafontaine P (2012) Angiotensin II reduces food intake by altering orexigenic neuropeptide expression in the mouse hypothalamus. Endocrinology 153:1411–1420
Grobe JL, Grobe CL, Beltz TG, Westphal SG, Morgan DA, Xu D, de Lange WJ, Li H, Sakai K, Thedens DR, Cassis LA, Rahmouni K, Mark AL, Johnson AK, Sigmund CD (2010) The brain renin-angiotensin system controls divergent efferent mechanisms to regulate fluid and energy balance. Cell Metabolism 12:431–442
Hilzendeger AM, Morgan DA, Brooks L, Dellsperger D, Liu X, Grobe JL, Rahmouni K, Sigmund CD, Mark AL (2012) A brain leptin–renin–angiotensin system interaction in the regulation of sympathetic nerve activity. American Journal of Physiology – Heart and Circulatory Physiology 303:H197–H206
Bełtowski J (2012) Leptin and the regulation of endothelial function in physiological and pathological conditions. Clinical and Experimental Pharmacology and Physiology 39: 168–178
Benkhoff S, Loot AE, Pierson I, Sturza A, Kohlstedt K, Fleming I, Shimokawa H, Grisk O, Brandes RP, Schröder K (2012) Leptin potentiates endothelium-dependent relaxation by inducing endothelial expression of neuronal NO synthase. Arteriosclerosis, Thrombosis, and Vascular Biology 32:1605–1612
Abboud FM, Floras JS, Aylward PE, Guo GB, Gupta BN, Schmid PG. Role of vasopressin in cardiovascular and blood pressure regulation. Blood Vessels 27:106–115
Koshimizu TA, Nasa Y, Tanoue A, Oikawa R, Kawahara Y, Kiyono Y, Adachi T, Tanaka T, Kuwaki T, Mori T, Takeo S, Okamura H, Tsujimoto G (2006) V1a vasopressin receptors maintain normal blood pressure by regulating circulating blood volume and baroreflex sensitivity. Proceedings of the National Academy of Sciences of the United States of America 103:7807–7812
Chassin C, Hornef MW, Bens M, Lotz M, Goujon JM, Vimont S, Arlet G, Hertig A, Rondeau E, Vandewalle A (2007) Hormonal control of the renal immune response and antibacterial host defense by arginine vasopressin. Journal of Experimental Medicine 204:2837–2852
Knepper MA, Star RA (2008) Vasopressin: friend or foe? Nature – Medicine 14:14–16
de Bold AJ (1985) Atrial natriuretic factor: a hormone produced by the heart. Science 230:767–770
Tsujita Y, Muraski J, Shiraishi I, Kato T, Kajstura J, Anversa P, Sussman MA (2006) Nuclear targeting of Akt antagonizes aspects of cardiomyocyte hypertrophy. Proceedings of the National Academy of Sciences of the United States of America 103:11946-11951
Suga SI, Itoh H, Komatsu Y, Ishida H, Igaki T, Yamashita J, Doi K, Chun TH, Yoshimasa T, Tanaka I, Nakao K (1998) Regulation of endothelial production of C-type natriuretic peptide by interaction between endothelial cells and macrophages. Endocrinology 139:1920–1926
Vesely BA, Eichelbaum EJ, Alli AA, Sun Y, Gower WR, Vesely DL (2006) Urodilatin and four cardiac hormones decrease human renal carcinoma cell numbers. European Journal of Clinical Investigation 36:810–819
Callaghan B, Hunne B, Hirayama H, Sartor DM, Nguyen TV, Abogadie FC, Ferens D, McIntyre P, Ban K, Baell J, Furness JB, Brock JA (2012) Sites of action of ghrelin receptor ligands in cardiovascular control. American Journal of Physiology – Heart and Circulatory Physiology 303:H1011–H1021
Hökfelt T, Lundberg JM, Schultzberg M, Johansson O, Skirboll L, Anggård A, Fredholm B, Hamberger B, Pernow B, Rehfeld J, Goldstein M (1980) Cellular localization of peptides in neural structures. Proceedings of the Royal Society of London. Series B, Biological Sciences 210:63–77
Sartor DM, Verberne AJ (2008) Abdominal vagal signalling: a novel role for cholecystokinin in circulatory control? Brain Research Reviews 59:140–154
Mahapatra NR (2008) Catestatin is a novel endogenous peptide that regulates cardiac function and blood pressure. Cardiovascular Research 80:330–338
Chap. 4. Physiology of the Ventilation
Bernard C (1966) Introduction à l’étude de médecine expérimentale [Introduction to the Study of Experimental Medicine]. Garnier – Flammarion, Paris
Dejours P (1981) Principles of Comparative Respiratory Physiology, Elsevier and North-Holland Biomedical Press, Amsterdam and New York
Atkins PW, de Paula J (2002) Physical Chemistry (7th Edition). Freeman WH, New York
Thiriet M, Douguet D, Bonnet JC, Canonne C, Hatzfeld C (1979) Influence du mélange He–O2 sur la mixique dans les bronchopneumopathies obstructives chroniques [Influence of a He–O2 mixture on gas mixing in chronic obstructive lung diseases]. Bulletin Européen de Physiopathologie Respiratoire 15:1053–1068
Cantor CR, Schimmel PR (1980) Biophysical Chemistry, Part 2: Techniques for the Study of Biological Structure and Function. Freeman WH, New York
Anonymous authors (2000-2013) Diffusion Time Calculator(www.physiologyweb.com)
Keener JP (2013) Mathematical Biology(www.math.utah.edu/keener/classes/math5120)
Mircea D, Panaitescu M (2013) Green Pack Online: Environmental Components – Air composition. The Regional Environmental Center for Central and Eastern Europe www.greenpackonline.org/english/environmental-components.php?id=01-01
Holt PG, Strickland DH, Wikström ME, Jahnse FL (2008) Regulation of immunological homeostasis in the respiratory tract. Nature Reviews – Immunology 8:142-152
Salathe M (2007) Regulation of mammalian ciliary beating. Annual Review of Physiology 69:401–422
Ingber DE (2006) Cellular mechanotransduction: putting all the pieces together again. FASEB Journal 20:811–827
Wright JL, Thurlbeck WM (2005) Quantitative Anatomy of the Lung. In: Churg AM, Myers JL, Tazelaar HD, Wright JL (eds), Thurlbeck’s Pathology of the Lung, third edition, Thieme, New York
Hart MC, Orzalesi MM, Cook CD (1963) Relation between anatomic respiratory dead space and body size and lung volume. Journal of Applied Physiology 18:519–522
Rafferty GF, Gardner WN (1996) Control of the respiratory cycle in conscious humans. Journal of Applied Physiology 81:1744–1753
Rafferty GF, Gardner WN (1995) Interaction between expiratory time and inspiration in conscious humans. Biological Psychology 41:96–97
Israël-Asselain R, Pocidalo JJ (1971) Respiration et maladies respiratoires. [Respiration and respiratory diseases]. In Vallery-Radot P, Hamburger J, Lhermitte F (eds.) Pathologie Mdicale. [Medical Pathology] (Vol.2), Flammarion Médecine Sciences, Paris
Fenn WO, Rahn H, and Otis AB (1946) A theoretical study of the composition of the alveolar air at altitude. American Journal of Physiology 146:637-653
Riley RL, Cournand A (1949) ”Ideal” alveolar air and the analysis of ventilation-perfusion relationships in the lungs. Journal of Applied Physiology 1:825–847
West JB, Dollery CT (1960) Distribution of blood flow and ventilation-perfusion ratio in the lung, measured with radioactive carbon dioxide. Journal of Applied Physiology 15:405–410
West JB (1970) Ventilation/Blood Flow and Gas Exchange. Blackwell, Oxford
Bates DV, Christie RV (1964) Respiratory Function in Disease, WB Saunders, Philadelphia
Brudin LH, Rhodes CG, Valind SO, Jones T, Hughes JM (1994) Interrelationships between regional blood flow, blood volume, and ventilation in supine humans. Journal of Applied Physiology 76:1205–1210
Wasserman DH, Whipp BJ (1983) Coupling of ventilation to pulmonary gas exchange during nonsteady-state work in men. Journal of Applied Physiology 54:587-593
Haouzi P (2006) Theories on the nature of the coupling between ventilation and gas exchange during exercise. Respiratory Physiology and Neurobiology 151:267–279
Altman PL, Dittmer DS [eds.] (1971) Biological Handbooks: Respiration and Circulation, Federation of American Societies for Experimental Biology, Bethesda, MD
Driehuys B, Cofer GP, Pollaro J, Mackel JB, Hedlund LW, Johnson GA (2006) Imaging alveolar-capillary gas transfer using hyperpolarized 129Xe MRI. Proceedings of the National Academy of Sciences of the United States of America 103:18278–18283
Kruhoffer P (1954) Lung diffusion coefficient for CO in normal human subjects by means of C14O. Acta Physiollogica Scandinavica 32:106–123.
Roughton FJW, Forster RE (1957) Relative importance of diffusion and chemical reaction in determining rate of exchange of gases in the human lung. Journal of Applied Physiology 11:290–302
Tartullier M, Ritz B, Ferrini M (1982) Physiologie de la Circulation Pulmonaire [Pulmonary Circulation Physiology]. In Denolin H (ed.) Physio-Pathologie Cardio-Pulmonaire [Cardiopulmonary Pathophysiology], SIMEP, Villeurbanne, France
Hartridge H, Roughton FJW (1923) Measurement of the rates of oxidation and reduction of haemoglobin. Nature 111:325–326
Hartridge H, Roughton FJW (1923) Method of measuring the velocity of very rapid chemical reactions. Proceedings of the Royal Society London Series A 104:376–394
Millikan GAA (1933) A simple photoelectric calorimeter. Journal of Physiology, London 79:158–179
Even P (1983) La respiration (p. 1087–1358). In Physiologie humaine, Meyer P (ed), Flammarion Médecine–Sciences, Paris
Yuan G, Peng YJ, Reddy VD, Makarenko VV, Nanduri J, Khan SA, Garcia JA, Kumar GK, Semenza GL, Prabhakar NR (2013) Mutual antagonism between hypoxia-inducible factors 1α and 2α regulates oxygen sensing and cardio-respiratory homeostasis. Proceedings of the National Academy of Sciences of the United States of America 110:E1788–E1796
Henderson LJ (1908) Concerning the relationship between the strength of acids and their capacity to preserve neutrality. American Journal of Physiology 21:173–179
Paton JFR, Abdala APL, Koizumi H, Smith JC, St-John WM (2006) Respiratory rhythm generation during gasping depends on persistent sodium current. Nature – Neuroscience 9:311–313
Feldman JL, Del Negro CA (2006) Looking for inspiration: new perspectives on respiratory rhythm. Nature Reviews – Neuroscience 7:232–241
Feldman JL, Kam K, Janczewski WA (2009) Practice makes perfect, even for breathing. Nature – Neuroscience 12:961 - 963
Tan W, Janczewski WA, Yang P, Shao XS, Callaway EM, Feldman JL (2008) Silencing preBötzinger complex somatostatin-expressing neurons induces persistent apnea in awake rat. Nature – Neuroscience 11:538–540
Bouvier J, Thoby-Brisson M, Renier N, Dubreuil V, Ericson J, Champagnat J, Pierani A, Chdotal A, Fortin G (2010) Hindbrain interneurons and axon guidance signaling critical for breathing. Nature – Neuroscience 13:1066–1074
Thoby-Brisson M, Karlén M, Wu N, Charnay P, Champagnat J, Fortin G (2009) Genetic identification of an embryonic parafacial oscillator coupling to the preBötzinger complex. Nature – Neuroscience 12:1028–1035
Gibson GG, Skett P (2001) Introduction to Drug Metabolism, Nelson Thornes Publishers, Cheltenham, UK
Capron M, Capron A, Goetzl EJ, Austen KF (1981) Tetrapeptides of the eosinophil chemotactic factor of anaphylaxis (ECF-A) enhance eosinophil Fc receptor. Nature 289:71–73
Sirois P, Borgeat P (1982) Leukotrienes: a new approach to the biochemistry of hypersensitivity. Survey of Immunologic Research l:279–285
Morris HR, Taylor GW, Jones CM, Scully N, Piper PJ, Tippins JR, Samhoun MN (1981) Structure elucidation and biosynthesis of slow reacting substances and slow reacting substance of anaphylaxis from guinea pig and human lungs. Progress in Lipid Research 20:719–725
Piper PJ (1978) Slow reacting substance of anaphylaxis. Annals of the Royal College of Surgeons of England 60:201–204
Gao X, Vockley CM, Pauli F, Newberry KM, Xue Y, Randell SH, Reddy TE, Hogan BL (2013) Evidence for multiple roles for grainyheadlike 2 in the establishment and maintenance of human mucociliary airway epithelium. Proceedings of the National Academy of Sciences of the United States of America 110:9356–9361
Guttinger M, Sutti F, Panigada M, Porcellini S, Merati B, Mariani M, Teesalu T, Consalez GG, Grassi F (1998) Epithelial V-like antigen (EVA), a novel member of the immunoglobulin superfamily, expressed in embryonic epithelia with a potential role as homotypic adhesion molecule in thymus histogenesis. Journal of Cell Biology 141:1061–1071
Wojcik E, Carrithers LM, Carrithers MD (2011) Characterization of epithelial V-like antigen in human choroid plexus epithelial cells: potential role in CNS immune surveillance. Neuroscience Letters 495:115–120
Yang CF, Hwu WL, Yang LC, Chung WH, Chien YH, Hung CF, Chen HC, Tsai PJ, Fann CS, Liao F, Chen YT (2008) A promoter sequence variant of ZNF750 is linked with familial psoriasis. Journal of Investigative Dermatology 128:1662–1668
Chung C, Kim T, Kim M, Kim M, Song H, Kim TS, Seo E, Lee SH, Kim H, Kim SK, Yoo G, Lee DH, Hwang DS, Kinashi T, Kim JM, Lim DS (2013) Hippo-Foxa2 signaling pathway plays a role in peripheral lung maturation and surfactant homeostasis. Proceedings of the National Academy of Sciences of the United States of America 110:7732–7737
Chap. 5. Medical Images and Physiological Signals
Bachelard G (1934) Le nouvel esprit scientifique [The New Scientific Spirit]. Presses Universitaires de France, Paris
Cebral JR, Löhner R (2001) From medical images to anatomically accurate finite element grids. International Journal for Numerical Methods in Engineering 51:985–1008
Thiriet M, Brugières P, Bittoun J, Gaston A (2001) Computational flow models in cerebral congenital aneurisms I: Steady flow. Revue Mcanique et Industries 2:107–118
Salmon S, Thiriet M, Gerbeau J-F (2003) Medical image-based computational model of pulsatile flow in saccular aneurisms. Mathematical Modelling and Numerical Analysis 37:663–679
Milner JS, Moore JA, Rutt BK, Steinman DA (1998) Hemodynamics of human carotid artery bifurcations: computational studies with models reconstructed from magnetic resonance imaging of normal subjects. Journal of Vascular Surgery 1998:143–156
Moore JA, Rutt BK, Karlik SJ, Yin K, Ethier CR (1999) Computational blood flow modeling based on in vivo measurements. Annals of Biomedical Engineering 27:627–640
Ladak HM, Milner JS, Steinman, DA (2000) Rapid 3D segmentation of the carotid bifurcation from serial MR images. Journal of Biomechanical Engineering 122:96–99
Papaharilaou Y, Doorly DJ, Sherwin SJ, Peiró J, Griffith C, Chesire N, Zervas V, Anderson J, Sanghera B, Watkins N, Caro CG (2002) Combined MRI and computational fluid dynamics detailed investigation of flow in idealised and realistic arterial bypass graft models. Biorheology 39:525–532
Gill JD, Ladak HM, Steinman DA, Fenster A (2000) Accuracy and variability assessment of a semiautomatic technique for segmentation of the carotid arteries from 3D ultrasound images. Medical Physics 27:1333–1342
de Feyter PJ (2012) CT functional imaging using intracoronary gradient analysis: an indispensable boost for CT coronary angiography. European Heart Journal – Cardiovasc Imaging 13:971–972
Choi JH, Koo BK, Yoon YE, Min JK, Song YB, Hahn JY, Choi SH, Gwon HC, Choe YH (2012) Diagnostic performance of intracoronary gradient-based methods by coronary computed tomography angiography for the evaluation of physiologically significant coronary artery stenoses: a validation study with fractional flow reserve. European Heart Journal – Cardiovasc Imaging 13:1001–1007
Thiriet M, Maarek JM, Chartrand DA, Delpuech C, Davis L, Hatzfeld C, Chang HK (1989) Transverse images of the human thoracic trachea during forced expiration. Journal of Applied Physiology 67:1032–1040
Bachelard G (1940) La philosophie du non: essai d’une philosophie du nouvel esprit scientifique [The Philosophy of No: a Philosophy of the New Scientific Mind]. Presses Universitaires de France, Paris
Bittoun J (1998) Basic principles of magnetic resonance imaging. In: Cerdan S, Haase A, Terrier F (eds.) Spectroscopy and Clinical MRI. Springer, New York
Singer JR (1959) Blood flow rates by nuclear magnetic resonance measurements. Science 130:1652–1653
McCready VR, Leach M, Ell PJ (1987) Functional Studies Using NMR. Springer, New York
Zerhouni EA, Parish DM, Rogers WJ, Yang A, Shapiro EP (1988) Human heart: tagging with MR imaging – a method for noninvasive assessment of myocardial motion. Radiology 169:59–63
Axel L, Dougherty L (1989) Heart wall motion: improved method of spatial modulation of magnetization for MR imaging. Radiology, 172:349–350
Mosher TJ, Smith MB (1990) A DANTE tagging sequence for the evaluation of translational sample motion. Magnetic Resonance in Medicine 15:334–339
Fischer SE, McKinnon GC, Maier SE, Boesiger P (1993) Improved myocardial tagging contrast. Magnetic Resonance in Medicine 30:191–200
McVeigh ER (1996) MRI of myocardial function: motion tracking techniques. Magnetic Resonance Imaging 14:137-150
Basser PJ, Mattiello J, LeBihan D (1994) MR diffusion tensor spectroscopy and imaging. Biophysical Journal 66:259–267
Hsu EW, Muzikant AL, Matulevicius SA, Penland RC, Henriquez CS (1998) Magnetic resonance myocardial fiber-orientation mapping with direct histological correlation. American Journal of Physiology – Heart and Circulatory Physiology 274:H1627–H1634
Scollan DF, Holmes A, Winslow R, Forder J (1998) Histological validation of reconstructed myocardial microstructure obtained from diffusion tensor magnetic resonance imaging. American Journal of Physiology – Heart and Circulatory Physiology 275 44:H2308–H2318
Helm PA, Tseng HJ, Younes L, McVeigh ER, Winslow RL (2005) Ex vivo 3D diffusion tensor imaging and quantification of cardiac laminar structure. Magnetic Resonance in Medicine 54:850-859
Winslow RL, Scollan DF, Holmes A, Yung CK, Zhang J, Jafri MS (2000) Electrophysiological modeling of cardiac ventricular function: from cell to organ. Annual Review of Biomedical Engineering 2:119–155
Papademetris X, Sinusas AJ, Dione DP, Constable RT, Duncan JS (2002) Estimation of 3-D left ventricular deformation from medical images using biomechanical models. IEEE Transactions on Medical Imaging 21:786–800
Sinusas AJ, Papademetris X, Constable RT, Dione DP, Slade MD, Shi P, Duncan JS (2001) Quantification of 3-D regional myocardial deformation: shape-based analysis of magnetic resonance images. American Journal of Physiology – Heart and Circulatory Physiology 281:698-714
Declerck J, Ayache N, McVeigh ER (1999) Use of a 4D planispheric transformation for the tracking and the analysis of LV motion with tagged MR images. In: Chen C-T, Clough AV (eds.) Medical Imaging 1999: Physiology and Function from Multidimensional Images. SPIE, Bellingham
Kozerke S, Scheidegger MB, Pedersen EM, Boesiger P (1999) Heart motion adapted cine phase-contrast flow measurements through the aortic valve. Magnetic Resonance in Medicine 42:970–978
Gleich B, Weizenecker J (2005) Tomographic imaging using the nonlinear response of magnetic particles. Nature 435:1214–1217
Ratnayaka K, Faranesh AZ, Hansen MS, Stine AM, Halabi M, Barbash IM, Schenke WH, Wright VJ, Grant LP, Kellman P, Kocaturk O, Lederman RJ (2013) Real-time MRI-guided right heart catheterization in adults using passive catheters. European Heart Journal 34: 380–389
Zimmerman JE, Theine P, Harding JT (1970) Design and operation of stable rf-biased superconducting point-contact quantum devices, and a note on the properties of perfectly clean metal contacts. Journal of Applied Physics 41:1572–1580
Cohen D, Edelsack EA, Zimmerman JE (1970) Magnetocardiograms taken inside a shielded room with a superconducting point-contact magnetometer. Applied Physics Letters 16: 278–280
Groeger S, Bison G, Knowles PE, Wynands R, Weis A (2006) Laser-pumped cesium magnetometers for high-resolution medical and fundamental research. Sensors and Actuators – A:Physical 129:1–5
Koch H (2004) Recent advances in magnetocardiography. Journal of Electrocardiology 37:117-122
Valsangiacomo Buechel ER, Mertens LL (2012) Imaging the right heart: the use of integrated multimodality imaging. European Heart Journal 33:949–960
Schaar JA, de Korte CL, Mastik F, Baldewsing R, Regar E, de Feyter P, Slager CJ, van der Steen AF, Serruys PW (2003) Intravascular palpography for high-risk vulnerable plaque assessment. Herz 28:488–495
Kanai H, Hasegawa H, Chubachi N, Koiwa Y, Tanaka M (1997) Noninvasive evaluation of local myocardial thickening and its color-coded imaging. IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control 44:752–768
Argyle RA, Ray SG (2009) Stress and strain: double trouble or useful tool? European Journal of Echocardiography 10:716–722
Leong-Poi H (2009) Molecular imaging using contrast-enhanced ultrasound: evaluation of angiogenesis and cell therapy. Cardiovascular Research 84:190–200
Todaro MC, Choudhuri I, Belohlavek M, Jahangir A, Carerj S, Oreto L, Khandheria BK (2012) New echocardiographic techniques for evaluation of left atrial mechanics. European Heart Journal – Cardiovascular Imaging 13:973–984
Ammar KA, Umland MM, Kramer C, Sulemanjee N, Jan MF, Khandheria BK, Seward JB, Paterick TE (2012) The ABCs of left ventricular assist device echocardiography: a systematic approach. European Heart Journal – Cardiovascular Imaging 13:885–899
Gutiérrez-Chico1 JL, Alegra-Barrero E, Teijeiro-Mestre R, Chan PH, Tsujioka H, de Silva R, Viceconte N, Lindsay A, Patterson T, Foin N, Akasaka T, di Mario C (2012) Optical coherence tomography: from research to practice. European Heart Journal – Cardiovascular Imaging 13:370–384
Prati F, Guagliumi G, Mintz GS, Costa M, Regar E, Akasaka T, Barlis P, Tearney GJ, Jang IK, Arbustini E, Bezerra HG, Ozaki Y, Bruining N, Dudek D, Radu M, Erglis A, Motreff P, Alfonso F, Toutouzas K, Gonzalo N, Tamburino C, Adriaenssens T, Pinto F, Serruys PW, Di Mario C; for the Expert’s OCT Review Document (2012) Expert review document part 2: methodology, terminology and clinical applications of optical coherence tomography for the assessment of interventional procedures. European Heart Journal 33:2513–2520.
Laughner JI, Zhang S, Li H, Shao CC, Efimov IR (2012) Mapping cardiac surface mechanics with structured light imaging. American Journal of Physiology – Heart and Circulatory Physiology 303:H712–H720
Thiberville L, Salaün M, Lachkar S, Dominique S, Moreno-Swirc S, Vever-Bizet C, Bourg-Heckly G (2009) Human in vivo fluorescence microimaging of the alveolar ducts and sacs during bronchoscopy. European Respiratory Journal 33:974–985
Moore JA, Steinman DA, Ethier CR (1998) Computational blood flow modelling: errors associated with reconstructing finite element models from magnetic resonance images. Journal of Biomechanics 31:179–184
Boissonnat J-D (1988) Shape reconstruction from planar cross-sections. Computer Vision, Graphics, and Image Processing 44:1–29
Boissonnat J-D, Chaine R, Frey P, Malandain G, Salmon S, Saltel E, Thiriet M (2005) From arteriographies to computational flow in saccular aneurisms: the INRIA experience. Medical Image Analysis 9:133–143
Boissonnat, J-D, Cazals F (2002) Smooth surface reconstruction via natural neighbour interpolation of distance functions. Computational Geometry 22:185–203
Osher S, Sethian JA (1988) Fronts propagating with curvature-dependent speed: algorithms based on Hamilton–Jacobi formulations. Journal of Computational Physics 79:12–49
Sethian, JA (1996) Level Set Methods: Evolving Interfaces in Geometry, Fluid Mechanics, Computer Vision, and Materials Science. Cambridge University Press, Cambridge
Lorensen, WE, Cline HE (1987) Marching cubes: a high resolution 3D surface construction algorithm. Computer Graphics 21:163–169
Delingette H, Hbert M, Ikeuchi K (1992) Shape representation and image segmentation using deformable surfaces. Image and Vision Computing 10:132–144
Taylor CA, Hughes TJR, Zarins CK (1998) Finite element modeling of blood flow in arteries. Computer Methods in Applied Mechanics and Engineering 158:155–196
Peiró J, Giordana S, Griffith C, Sherwin SJ (2002) High-order algorithms for vascular flow modelling. International Journal for Numerical Methods in Fluids 40:137–151
Sherwin SJ, Peiró J (2002) Mesh generation in curvilinear domains using high-order elements. International Journal for Numerical Methods in Engineering 53:207–223
Giachetti A, Tuveri M, Zanetti G (2003) Reconstruction and web distribution of measurable arterial models. Medical Image Analysis 7:79–93
Cohen LD (1991) On active contour models and balloons. Computer Vision, Graphics, and Image Processing 53:211–218
Xu C, Prince JL (1998) Snakes, shapes and gradient vector flow. IEEE Transactions on Image Processing 7:359–369
McInerney T, Terzopoulos D (1995) Topologically adaptable snakes. In: Proceedings of the fifth international conference on computer vision. IEEE
Krissian K, Malandain G, Ayache N (1998) Model based multiscale detection and reconstruction of 3D vessels. INRIA Research Report RR-3442
Fetita C, Prteux F, Beigelman-Aubry C, Grenier P (2004) Pulmonary airways: 3D reconstruction from multi-slice CT and clinical investigation, IEEE Transactions on Medical Imaging 23:1353–1364
Perchet D, Fetita CI, Vial L, Prteux F, Sbirlea-Apiou G, Thiriet M (2004) Virtual investigation of pulmonary airways in volumetric computed tomography, Computer Animation and Virtual Worlds 15:361–376
George P-L, Hecht H, Saltel E (1990) Fully automatic mesh generator for 3D domains of any shape. Impact of Computing in Science and Engineering 2:187–218
George P-L (1990) Gnration automatique de maillages [Automatic Mesh Generation]. Masson, Paris
George P-L, Borouchaki H (1997) Triangulation de Delaunay et maillage [Delaunay Triangulation and Mesh]. Hermès, Paris
Frey PJ, George P-L (1999) Maillages [Meshes]. Hermès, Paris
George P-L, Hecht F (1999), Nonisotropic grid. In: Thompson JF, Soni BK, Weatherill NP (eds.) Handbook of Grid Generation. CRC Press, Boca Raton, FL
Mohammadi B, George P-L, Hecht F, Saltel, E (2000) 3D Mesh adaptation by metric control for CFD. Revue europenne des lments finis 9:439–449
Habashi WG, Dompierre J, Bourgault Y, Fortin M, Vallet M-G (1998) Certifiable computational fluid mechanics through mesh optimization. AIAA Journal 36:703–711
Fortin, M (2000) Anisotropic mesh adaptation through hierarchical error estimators. In: Minev, P, Yanping L (eds.) Scientific Computing and Applications. Nova Science, Commack, NY
Dompierre J, Vellet M-G, Bourgault Y, Fortin M, Habashi WG (2002) Anisotropic mesh adaptation: towards user-independent, mesh-independent and solver-independent CFD III: Unstructured meshes. International Journal for Numerical Methods in Fluids 39:675–702
Fortin A, Bertrand F, Fortin M, Boulanger-Nadeau PE, El Maliki A, Najeh N (2004) Adaptive remeshing strategy for shear-thinning fluid flow simulations. Computers and Chemical Engineering 28:2363–2375
Cebral JR, Lohner R (2001) From medical images to anatomically accurate finite element grids. International Journal for Numerical Methods in Engineering 51:985–1008
Taubin G (1995) Curve and surface smoothing without shrinkage. In: Proceedings of the Fifth International Conference on Computer Vision. IEEE
Frey PJ, Borouchaki H (1998) Geometric surface mesh optimization. Computing and Visualization in Science 1:113–121
Thiriet M, Graham JMR, Issa RI (1992) A pulsatile developing flow in a bend. Journal de Physique III 2:995–1013
Frey PJ, Borouchaki H (2003) Surface meshing using a geometric error estimate. International Journal for Numerical Methods in Engineering 58:227–245
Belhamadia Y, Fortin A, Chamberland E (2004) Anisotropic mesh adaptation for the solution of the Stefan problem. Journal of Computational Physics 194:233–255
Belhamadia Y, Fortin A, Chamberland E (2004) Three-dimensional anisotropic mesh adaptation for phase change problems, Journal of Computational Physics 201:753–770
McGraw-Hill Encyclopedia of Science and Technology (1960) McGraw-Hill, New York
Conrad WA, McQueen DM, Yellin EL (1980) Steady pressure flow relations in compressed arteries: Possible origin of Korotkoff sounds. Medical and Biological Engineering and Computing 18:419–426
Risacher F (1995) tude de la propagation de l’onde de pouls par plthysmographie d’impdance lectrique [Study of the propagation of pulse waves by electric impedance plethysmography]. PhD Thesis, University Claude Bernard, Lyon
O’Rourke MF, Avolio AP, Kelly RP (1992) The Arterial Pulse. Lea & Febiger, Baltimore, MD
Penaz J (1992) Criteria for set point estimation in the volume clamp method of blood pressure measurement. Physiological Research 41:5–10
Williams B, Lacy PS (2010) Central haemodynamics and clinical outcomes: going beyond brachial blood pressure? European Heart Journal 31:1819–1822
Vlachopoulos C, Aznaouridis K, O’Rourke MF, Safar ME, Baou K, Stefanadis C (2010) Prediction of cardiovascular events and all-cause mortality with central haemodynamics: a systematic review and meta-analysis. European Heart Journal 31:1865–1871
Omboni S, Parati G, Frattola A, Mutti E, Di Rienzo M, Castiglioni P, Mancia G (1993) Spectral and sequence analysis of finger blood pressure variability. Comparison with analysis of intra-arterial recordings. Hypertension 22:26–33
Novak V, Novak P, Schondorf R (1994) Accuracy of beat-to-beat noninvasive measurement of finger arterial pressure using the Finapres: a spectral analysis approach. Journal of Clinical Monitoring 10:118–126
Imholz BP, Wieling W, van Montfrans GA, Wesseling KH (1998) Fifteen years experience with finger arterial pressure monitoring: assessment of the technology. Cardiovascular Research 38:605–616
Coron J-M, Crpeau E (2003) Exact boundary controllability of a nonlinear KdV equation with critical lengths. INRIA Research Report RR-5000
Whitman GB (1999) Linear and Nonlinear Waves. Wiley-Interscience, New York
Crpeau E, Sorine M (2005) personal communication
Tasu J-P, Mousseaux E, Colin P, Slama MS, Jolivet O, Bittoun J (2002) Estimation of left ventricle performance through temporal pressure variations measured by MR velocity and acceleration mappings. Journal of Magnetic Resonance Imaging 16:246–252
Laleg TM, Crépeau E, Papelier Y, Sorine M (2007) Arterial blood pressure analysis based on scattering transform. 29th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (IEEE EMBC), Lyon, France
Kitney RI, Giddens DP (1983) Analysis of blood velocity waveforms by phase shift averaging and autoregressive spectral estimation. Journal of Biomechanical Engineering 105:398–401
Thiriet M, Cybulski G, Darrow RD, Doorly DJ, Dumoulin C, Tarnawski M, Caro CG (1997) Apports et limitations de la vlocimtrie par rsonance magntique nuclaire en biomcanique. Mesures dans un embranchement plan symtrique [Contributions and limitations of the nuclear magnetic resonance velocimetry in biomechanics. Measures in a two plane symmetrical bifurcation]. Journal de Physique III 7:771–787
Durand E, Guillot G, Darrasse L, Tastevin G, Nacher PJ, Vignaud A, Vattolo D, Bittoun J (2002) CPMG measurements and ultrafast imaging in human lungs with hyperpolarized helium-3 at low field (0.1 T). Magnetic Resonance in Medicine 47:75–81
de Rochefort L., Vial L., Fodil R., Maître X., Louis B., Isabey D., Caillibotte G., Thiriet M., Bittoun J., Durand E., Sbirlea-Apiou G. (2007) In vitro validation of CFD simulation in human proximal airways reconstructed from medical images with hyperpolarized helium-3 MRI phase contrast velocimetry. Journal of Applied Physiology: Respiratory, Environmental and Exercise Physiology 102:2012–2023
Dumoulin CL, Hart HR Jr (1986) Magnetic resonance angiography. Radiology 161 717–720
Dumoulin CL, Souza SP, Hart HR (1987) Rapid scan magnetic resonance angiography. Magnetic Resonance in Medicine 5:238–245
Dumoulin CL, Souza SP, Walker MF, Yoshitome E (1988) Time-resolved magnetic resonance angiography. Magnetic Resonance in Medicine 6:275–286
Dumoulin CL, Souza SP, Walker MF, Wagle W (1989) Three-dimensional phase contrast angiography. Magnetic Resonance in Medicine 9:139–149
Dumoulin CL, Doorly DJ, Caro CG (1993) Quantitative measurement of velocity at multiple positions using comb excitation and Fourier velocity encoding. Magnetic Resonance in Medicine 29:44–52
Bittoun J, Jolivet O, Herment A, Itti E, Durand E, Mousseaux E, Tasu J-P (2000) Multidimensional MR mapping of multiple components of velocity and acceleration by Fourier phase encoding with a small number of encoding steps. Magnetic Resonance in Medicine 44:723–730
Durand E, Jolivet O, Itti E, Tasu J-P, Bittoun J (2001) Precision of magnetic resonance velocity and acceleration measurements: theoreticals issues and phantom experiments. Magnetic Resonance in Medicine 13:445–451
Liebman FM, Pearl J, Bagnol S (1962) The electrical conductance properties of blood in motion. Physics in Medicine and Biology 7:177–194
Geddes LA, Sadler C (1973) The specific resistance of blood at body temperature. Medical and Biological Engineering 11:336–339
Brody DA (1956) A theoretical analysis of intracavitary blood mass influence on the heart-lead relationship. Circulation Research 4:731–738
Gulrajani RM, Roberge FA, Mailloux GE (1989) The forward problem of electrocardiography. In Comprehensive Electrocardiology: Theory and Practice in Health and Disease. Macfarlane PW, Lawrie TDV (eds.), 237–288, Pergamon Press, New York
Einthoven W (1895) Uber die Form des menschlichen Electrokardiograms [On the shape of the electrocardiogram in men]. Pflügers Archiv fur die gesamte Physiologie des Menschen und der Tiere 60:101-123
Einthoven W (1908) Weiteres über das Elektrokardiogram [More on the electrocardiogram]. Pflügers Archiv fur die gesamte Physiologie des Menschen und der Tiere 122:517–548
Einthoven W, Fahr G, de Waart A (1913) Uber die Richtung und die Manifeste Grösse der Potentialschwankungen im mennschlichen Herzen und über den Einfluss der Herzlage auf die Form des Elektrokardiogramms [On the direction and manifest size of the variations of potential in the human heart and on the influence of the heart position in the shape of the electrocardiogram]. Pflügers Archiv fur die gesamte Physiologie des Menschen und der Tiere 150:275-315
Goldberger E (1942) The aVL, aVR, and aVF leads. A simplification of standard lead electrocardiography. American Heart Journal 24:378–396
Einthoven W, Fahr G, de Waart A (1950) On the direction and manifest size of the variations of potential in the human heart and on the influence of the position of the heart on the form of the electrocardiogram. American Heart Journal 40:163–211
Baumert M, Lambert GW, Dawood T, Lambert EA, Esler MD, McGrane M, Barton D, Nalivaiko E (2008) QT interval variability and cardiac norepinephrine spillover in patients with depression and panic disorder. American Journal of Physiology – Heart and Circulatory Physiology 295:H962–H968
Boulakia M, Fernández MA, Gerbeau JF, Zenzemi N (2007) Numerical simulation of ECG. Functional Imaging and Modeling of the Heart: FIMH07, Springer, NY
Frank E (1956) An accurate, clinically practical system for spatial vectorcardiography. Circulation 13: 737–749
Nousiainen J, Oja S, Malmivuo J (1994) Normal vector magnetocardiogram. I. Correlation with the normal vector ECG. Journal of Electrocardiology 27:221–231
Nousiainen J, Oja S, Malmivuo J (1994) Normal vector magnetocardiogram. II. Effect of constitutional variables. Journal of Electrocardiology 27:233–241
Baule GM, McFee R (1963) Detection of the magnetic field of the heart. American Heart Journal 66:95–96
van Oosterom A, Oostendorp TF, Huiskamp GJ, ter Brake HJ (1990) The magnetocardiogram as derived from electrocardiographic data. Circulation Research 67:1503–1509
Penney BC (1986) Theory and cardiac applications of electrical impedance measurements. CRC Critical Reviews in Biomedical Engineering 13:227-281
Cybulski G (2005) Dynamic impedance cardiography – the system and its applications. Polish Journal of Medical Physics and Engineering 11:127–209
Mead J, Whittenberger JL (1953) Physical properties of human lungs measured during spontaneous respiration. Journal of Applied Physiology 5:779–796
DuBois AB, Botelho SY, Comroe JH (1956) A new method for measuring airway resistance in man using a body plethysmograph: values in normal subjects and in patients with respiratory disease. Journal of Clinical Investigation 35:327–335
Jaeger MJ, Otis AB (1964) Measurement of airway resistance with a volume displacement body plethysmograph. Journal of Applied Physiology 19:813–819
Rice DA (1980) Sound speed in the upper airways. Journal of Applied Physiology 49: 326–336
Rice DA (1983) Sound speed in pulmonary parenchyma. Journal of Applied Physiology 54:304–308
Scherer PW, Shendalman LH, Greene NM, Bouhuys A (1975) Measurement of axial diffusivities in a model of the bronchial airways. Journal of Applied Physiology 38:719–723
Ultman JS, Blatman HS (1977) Longitudinal mixing in pulmonary airways. Analysis of inert gas dispersion in symmetric tube network models. Respiration physiology 30:349–367
Grubb BR, Mills CD (1981) Blood oxygen content in microliter samples using an easy-to-build galvanic oxygen cell. Journal of Applied Physiology 50:456-464
Krogh A, Krogh M (1909) Rate of diffusion into lungs of man. Skandinavisches Archiv für Physiologie 23:236–247
Krogh A (1909) On the mechanism of gas exchange in the lungs. Skandinavisches Archiv für Physiologie 23:248–278
Krogh M (1915) The diffusion of gases through the lungs of man. Journal of Physiology, London 49:271–296
Forster RE, Fowler WS, Bates DV (1954) The absorption of carbon monoxide by the lungs during breathholding. Journal of Clinical Investigation 33:1135–1145
Roughton FJW, Forster RE (1957) Relative importance of diffusion and chemical reaction in determining rate of exchange of gases in the human lung. Journal of Applied Physiology 11:290–302
Burrows B, Kasik JE, Niden AH, Barclay WR (1961) Clinical usefulness of the single-breath pulmonucy diffusing capacity test. American Review of Respiratory Diseases 84:789–806
Hughes JMB, Bates DV (2003) Historical review: the carbon monoxide diffusing capacity and its membrane and red cell components. Respiratory Physiology and Neurobiology 138:115–142
Widdicombe J (1997) Airway and alveolar permeability and surface liquid thickness: theory. Journal of Applied Physiology 82:3–12
Conclusion
Kobori H, Nangaku M, Navar LG, Nishiyama A (2007) The intrarenal renin-angiotensin system: from physiology to the pathobiology of hypertension and kidney disease. Pharmacological Reviews 59:251–287
Fitzsimons JT (1998) Angiotensin, thirst, and sodium appetite. Physiological Reviews 78:583–686
Beuschlein F (2013) Regulation of aldosterone secretion: from physiology to disease. European Journal of Endocrinology 168:R85–R93
Appendices
Hoffmann R, Valencia A (2004) A gene network for navigating the literature. Nature – Genetics 36:664 (Information Hyperlinked over Proteins. www.ihop-net.org)
BioGRID: General Repository for Interaction Datasets; database of physical and genetic interactions for model organisms (www.thebiogrid.org)
GeneCards human gene database. Crown Human Genome Center, Department of Molecular Genetics, the Weizmann Institute of Science (www.genecards.org)
Universal Protein Resource (UniProt) Consortium (European Bioinformatics Institute, Swiss Institute of Bioinformatics, and Protein Information Resource. www.uniprot.org)
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Thiriet, M. (2014). Medical Images and Physiological Signals. In: Anatomy and Physiology of the Circulatory and Ventilatory Systems. Biomathematical and Biomechanical Modeling of the Circulatory and Ventilatory Systems, vol 6. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-9469-0_5
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