Abstract
Modern cerebrospinal fluid (CSF) physiologic investigation accelerated after World War II with the advent of radio-isotopes to quantify choroid plexus (CP) ion transport and CSF flow dynamics. Hugh Davson, Malcolm Segal, Michael Bradbury, Michael Pollay, Keasley Welch, Helen Cserr, John Pappenheimer, and colleagues, developed laboratory preparations to assess tracer uptake/release by CP and associated flow dynamics within the ventricular-brain system. This canonical research established several basic physiologic concepts: differences between CP and blood-brain barrier, CP as primary site of CSF formation, ependymal permeability, intimate CSF and brain interstitial fluid association, CSF sink action for excretion, and a quasi-lymphatic function of CSF flow/drainage to cervical lymph. Their seminal findings constitute a reliable foundation on which to build contemporary models of CP transport/CSF dynamics, including functional interaction with the newly-described glymphatic system. The 1980s–1990s provided research findings on CSF regulation by neurotransmitters and neuropeptides; also, many new pharmacologic agents were tested for controlling CSF formation. Over the past 2–3 decades, the advent/refinement of diverse immunohistochemical, neuroendocrine and molecular techniques has delineated the expression and function of basolateral and apical transporters at the blood-CSF interface. Recently, CP gene knock-out models and transcriptomic approaches have engendered specific analysis of CP transport and metabolism. Increasing attention is being paid to the CP role in diseases such as Alzheimer’s, Parkinson’s, stroke, intracranial hypertension and hydrocephalus. The physiologic impact of CP-CSF fluid generation, pressure and homeostasis on the putative glymphatic system is a promising topic. There is an increasing need to blend transport/fluid phenomena at the BCSFB with the BBB and ependymal CSF-brain interface. Integrated models that incorporate all CNS transport interfaces will provide a key impetus for advances in translational neuromedicine.
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References
Abbott NJ, Pizzo ME, Preston JE, Janigro D, Thorne RG (2018) The role of brain barriers in fluid movement in the CNS: is there a ‘glymphatic’ system? Acta Neuropathol 135(3):387–407
Adamson RH, Lenz JF, Zhang X, Adamson GN, Weinbaum S, Curry FE (2004) Oncotic pressures opposing filtration across non-fenestrated rat microvessels. J Physiol 557(Pt 3):889–907
Adamson SX, Shen X, Jiang W, Lai V, Wang X, Shannahan JH et al (2018) Subchronic manganese exposure impairs neurogenesis in the adult rat hippocampus. Toxicol Sci 163(2):592–608
Agnati LF, Bjelke B, Fuxe K (1995) Volume versus wiring transmission in the brain: a new theoretical frame for neuropsychopharmacology. Med Res Rev 15(1):33–45
Akdemir G, Luer MS, Dujovny M, Misra M (1997) Intraventricular atrial natriuretic peptide for acute intracranial hypertension. Neurol Res 19(5):515–520
Albrecht P, Lewerenz J, Dittmer S, Noack R, Maher P, Methner A (2010) Mechanisms of oxidative glutamate toxicity: the glutamate/cystine antiporter system xc- as a neuroprotective drug target. CNS Neurol Disord Drug Targets 9(3):373–382
Aldred AR, Brack CM, Schreiber G (1995) The cerebral expression of plasma protein genes in different species. Comp Biochem Physiol B Biochem Mol Biol 111(1):1–15
Allonen H, Anderson KE, Iisalo E, Kanto J, Stromblad LG, Wettrell G (1977) Passage of digoxin into cerebrospinal fluid in man. Acta Pharmacol Toxicol 41(3):193–202
Andersen HH, Johnsen KB, Moos T (2014) Iron deposits in the chronically inflamed central nervous system and contributes to neurodegeneration. Cell Mol Life Sci 71(9):1607–1622
Anderson DK, Heisey SR (1975) Creatinine, potassium, and calcium flux from chicken cerebrospinal fluid. Am J Phys 228(2):415–419
Anonymous (1998) International randomised controlled trial of acetazolamide and furosemide in posthaemorrhagic ventricular dilatation in infancy. International PHVD Drug Trial Group. Lancet (London, England) 352(9126):433–440
Arregui A, Iversen LL (1978) Angiotensin-converting enzyme: presence of high activity in choroid plexus of mammalian brain. Eur J Pharmacol 52(1):147–150
Aspelund A, Antila S, Proulx ST, Karlsen TV, Karaman S, Detmar M et al (2015) A dural lymphatic vascular system that drains brain interstitial fluid and macromolecules. J Exp Med 212(7):991–999
Balin BJ, Broadwell RD (1988) Transcytosis of protein through the mammalian cerebral epithelium and endothelium. I. Choroid plexus and the blood-cerebrospinal fluid barrier. J Neurocytol 17(6):809–826
Batllori M, Molero-Luis M, Ormazabal A, Montero R, Sierra C, Ribes A et al (2018) Cerebrospinal fluid monoamines, pterins, and folate in patients with mitochondrial diseases: systematic review and hospital experience. J Inherit Metab Dis 41:1147–1158
Bergen AA, Kaing S, ten Brink JB, Gorgels TG, Janssen SF, Bank NB (2015) Gene expression and functional annotation of human choroid plexus epithelium failure in Alzheimer’s disease. BMC Genomics 16:956
Bering EA Jr (1955) Choroid plexus and arterial pulsation of cerebrospinal fluid; demonstration of the choroid plexuses as a cerebrospinal fluid pump. AMA Arch Neurol Psychiatry 73(2):165–172
Betz AL, Firth JA, Goldstein GW (1980) Polarity of the blood-brain barrier: distribution of enzymes between the luminal and antiluminal membranes of brain capillary endothelial cells. Brain Res 192(1):17–28
Bezerra MLS, Ferreira ACAF, de Oliveira-Souza R (2017) Pseudotumor cerebri and glymphatic dysfunction. Front Neurol 8:734
Birzis L, Carter CH, Maren TH (1958) Effects of acetazolamide on CSF pressure and electrolytes in hydrocephalus. Neurology 8(7):522–528
Black PM (1999) Harvey Cushing at the Peter Bent Brigham Hospital. Neurosurgery 45(5):990–1001
Boland B, Yu WH, Corti O, Mollereau B, Henriques A, Bezard E et al (2018) Promoting the clearance of neurotoxic proteins in neurodegenerative disorders of ageing. Nat Rev Drug Discov 17:660–688
Borlongan CV, Skinner SJ, Geaney M, Vasconcellos AV, Elliott RB, Emerich DF (2004) Intracerebral transplantation of porcine choroid plexus provides structural and functional neuroprotection in a rodent model of stroke. Stroke 35(9):2206–2210
Boyson SJ, Alexander A (1990) Net production of cerebrospinal fluid is decreased by SCH-23390. Ann Neurol 27(6):631–635
Bradbury MW, Cserr HF, Westrop RJ (1981) Drainage of cerebral interstitial fluid into deep cervical lymph of the rabbit. Am J Phys 240(4):F329–F336
Brinker T, Stopa E, Morrison J, Klinge P (2014) A new look at cerebrospinal fluid circulation. Fluids Barriers CNS 11:10
Cains S, Shepherd A, Nabiuni M, Owen-Lynch PJ, Miyan J (2009) Addressing a folate imbalance in fetal cerebrospinal fluid can decrease the incidence of congenital hydrocephalus. J Neuropathol Exp Neurol 68(4):404–416
Carro E, Trejo JL, Spuch C, Bohl D, Heard JM, Torres-Aleman I (2006a) Blockade of the insulin-like growth factor I receptor in the choroid plexus originates Alzheimer’s-like neuropathology in rodents: new cues into the human disease? Neurobiol Aging 27(11):1618–1631
Carro E, Trejo JL, Gerber A, Loetscher H, Torrado J, Metzger F et al (2006b) Therapeutic actions of insulin-like growth factor I on APP/PS2 mice with severe brain amyloidosis. Neurobiol Aging 27(9):1250–1257
Cherian I, Bernardo A, Grasso G (2016) Cisternostomy for traumatic brain injury: pathophysiologic mechanisms and surgical technical notes. World Neurosurg 89:51–57
Chodobski A, Szmydynger-Chodobska J, Vannorsdall MD, Epstein MH, Johanson CE (1994) AT1 receptor subtype mediates the inhibitory effect of central angiotensin II on cerebrospinal fluid formation in the rat. Regul Pept 53(2):123–129
Chodobski A, Loh YP, Corsetti S, Szmydynger-Chodobska J, Johanson CE, Lim YP et al (1997) The presence of arginine vasopressin and its mRNA in rat choroid plexus epithelium. Brain Res Mol Brain Res 48(1):67–72
Chodobski A, Szmydynger-Chodobska J, Johanson CE (1998) Vasopressin mediates the inhibitory effect of central angiotensin II on cerebrospinal fluid formation. Eur J Pharmacol 347(2–3):205–209
Chodobski A, Szmydynger-Chodobska J, Johanson CE (1999) Angiotensin II regulates choroid plexus blood flow by interacting with the sympathetic nervous system and nitric oxide. Brain Res 816(2):518–526
Christensen HL, Nguyen AT, Pedersen FD, Damkier HH (2013) Na(+) dependent acid-base transporters in the choroid plexus; insights from slc4 and slc9 gene deletion studies. Front Physiol 4:304
Christensen HL, Barbuskaite D, Rojek A, Malte H, Christensen IB, Fuchtbauer AC et al (2018) The choroid plexus sodium-bicarbonate cotransporter NBCe2 regulates mouse cerebrospinal fluid pH. J Physiol 596:4709–4728
Clardy SL, Wang X, Boyer PJ, Earley CJ, Allen RP, Connor JR (2006) Is ferroportin-hepcidin signaling altered in restless legs syndrome? J Neurol Sci 247(2):173–179
Cruz Y, García EE, Gálvez JV, Arias-Santiago SV, Carvajal HG, Silva-García R et al (2018) Release of interleukin-10 and neurotrophic factors in the choroid plexus: possible inductors of neurogenesis following copolymer-1 immunization after cerebral ischemia. Neural Regen Res 13(10):1743–1752
Cserr HF (1971) Physiology of the choroid plexus. Physiol Rev 51(2):273–311
Cserr HF (1988) Role of secretion and bulk flow of brain interstitial fluid in brain volume regulation. Ann N Y Acad Sci 529:9–20
Cserr HF, VanDyke DH (1971) 5-Hydroxyindoleacetic acid accumulation by isolated choroid plexus. Am J Phys 220(3):718–723
Curry FE, Frokjaer-Jensen J (1984) Water flow across the walls of single muscle capillaries in the frog, Rana pipiens. J Physiol 350:293–307
Dai YB, Wu WF, Huang B, Miao YF, Nadarshina S, Warner M et al (2016) Liver X receptors regulate cerebrospinal fluid production. Mol Psychiatry 21(6):844–856
Damkier HH, Brown PD, Praetorius J (2013) Cerebrospinal fluid secretion by the choroid plexus. Physiol Rev 93(4):1847–1892
Davson H, Segal MB (1970) The effects of some inhibitors and accelerators of sodium transport on the turnover of 22Na in the cerebrospinal fluid and the brain. J Physiol 209(1):131–153
Deignan JL, De Deyn PP, Cederbaum SD, Fuchshuber A, Roth B, Gsell W et al (2010) Guanidino compound levels in blood, cerebrospinal fluid, and post-mortem brain material of patients with argininemia. Mol Genet Metab 100(Suppl 1):S31–S36
Del Bigio MR (1995) The ependyma: a protective barrier between brain and cerebrospinal fluid. Glia 14(1):1–13
Doczi T, Joo F, Vecsernyes M, Bodosi M (1988) Increased concentration of atrial natriuretic factor in the cerebrospinal fluid of patients with aneurysmal subarachnoid hemorrhage and raised intracranial pressure. Neurosurgery 23(1):16–19
Du Y, Wu HT, Qin XY, Cao C, Liu Y, Cao ZZ et al (2018) Postmortem brain, cerebrospinal fluid, and blood neurotrophic factor levels in Alzheimer’s disease: a systematic review and meta-analysis. J Mol Neurosci 65(3):289–300
Engelhardt B, Ransohoff RM (2012) Capture, crawl, cross: the T cell code to breach the blood-brain barriers. Trends Immunol 33(12):579–589
Faraci FM, Heistad DD (1992) Does basal production of nitric oxide contribute to regulation of brain-fluid balance? Am J Phys 262(2 Pt 2):H340–H344
Faraci FM, Mayhan WG, Heistad DD (1990) Effect of vasopressin on production of cerebrospinal fluid: possible role of vasopressin (V1)-receptors. Am J Phys 258(1 Pt 2):R94–R98
Farthing CA, Sweet DH (2014) Expression and function of organic cation and anion transporters (SLC22 family) in the CNS. Curr Pharm Des 20(10):1472–1486
Fenstermacher JD, Johnson JA (1966) Filtration and reflection coefficients of the rabbit blood-brain barrier. Am J Phys 211(2):341–346
Fenstermacher JD, Ghersi-Egea JF, Finnegan W, Chen JL (1997) The rapid flow of cerebrospinal fluid from ventricles to cisterns via subarachnoid velae in the normal rat. Acta Neurochir Suppl 70:285–287
Fraser PA, Dallas AD, Davies S (1990) Measurement of filtration coefficient in single cerebral microvessels of the frog. J Physiol 423:343–361
Gath U, Hakvoort A, Wegener J, Decker S, Galla HJ (1997) Porcine choroid plexus cells in culture: expression of polarized phenotype, maintenance of barrier properties and apical secretion of CSF-components. Eur J Cell Biol 74(1):68–78
Gerstberger R, Schütz H, Luther-Dyroff D, Keil R, Simon E (1992) Inhibition of vasopressin and aldosterone release by atrial natriuretic peptide in conscious rabbits. Exp Physiol 77(4):587–600
Ghersi-Egea JF, Finnegan W, Chen JL, Fenstermacher JD (1996) Rapid distribution of intraventricularly administered sucrose into cerebrospinal fluid cisterns via subarachnoid velae in rat. Neuroscience 75(4):1271–1288
Gibbs JE, Thomas SA (2005) Choroid plexus and drug therapy for AIDS encephalopathy. In: Zheng W, Chodobski A (eds) The blood-cerebrospinal fluid barrier. CRC/Taylor & Francis Group, Boca Raton, FL, pp 391–411
González Burgos GR, Rosenstein RE, Cardinali DP (1994) Daily changes in presynaptic cholinergic activity of rat sympathetic superior cervical ganglion. Brain Res 636(2):181–186
Gregoriades JMC, Madaris A, Alvarez FJ, Alvarez-Leefmans FJ (2019) Genetic and pharmacological inactivation of apical Na+-K+-2Cl- cotransporter 1 in choroid plexus epithelial cells reveals the physiological function of the cotransporter. Am J Physiol Cell Physiol 316(4):C525–CC44
Groger N, Vitzthum H, Frohlich H, Kruger M, Ehmke H, Braun T et al (2012) Targeted mutation of SLC4A5 induces arterial hypertension and renal metabolic acidosis. Hum Mol Genet 21(5):1025–1036
Grove KL, Goncalves J, Picard S, Thibault G, Deschepper CF (1997) Comparison of ANP binding and sensitivity in brains from hypertensive and normotensive rats. Am J Phys 272(4 Pt 2):R1344–R1353
Gudasheva TA, Povarnina PY, Antipova TA, Seredenin SB (2018) Dipeptide mimetic of the BDNF GSB-106 with antidepressant-like activity stimulates synaptogenesis. Dokl Biochem Biophys 481(1):225–227
Guerreiro PM, Bataille AM, Parker SL, Renfro JL (2014) Active removal of inorganic phosphate from cerebrospinal fluid by the choroid plexus. Am J Physiol Renal Physiol 306(11):F1275–F1284
Haj-Yasein NN, Vindedal GF, Eilert-Olsen M, Gundersen GA, Skare O, Laake P et al (2011) Glial-conditional deletion of aquaporin-4 (Aqp4) reduces blood-brain water uptake and confers barrier function on perivascular astrocyte endfeet. Proc Natl Acad Sci U S A 108(43):17815–17820
Hakvoort A, Haselbach M, Wegener J, Hoheisel D, Galla HJ (1998) The polarity of choroid plexus epithelial cells in vitro is improved in serum-free medium. J Neurochem 71(3):1141–1150
Hartig PR, Hoffman BJ, Kaufman MJ, Hirata F (1990) The 5-HT1C receptor. Ann N Y Acad Sci 600:149–166. discussion 66–67
Hartz AM, Bauer B (2011) ABC transporters in the CNS – an inventory. Curr Pharm Biotechnol 12(4):656–673
Haywood JR, Vogh BP (1979) Some measurements of autonomic nervous system influence on production of cerebrospinal fluid in the cat. J Pharmacol Exp Ther 208(2):341–346
Herbute S, Oliver J, Davet J, Viso M, Ballard RW, Gharib C et al (1994) ANP binding sites are increased in choroid plexus of SLS-1 rats after 9 days of spaceflight. Aviat Space Environ Med 65(2):134–138
Herrick-Davis K, Grinde E, Lindsley T, Teitler M, Mancia F, Cowan A et al (2015) Native serotonin 5-HT2C receptors are expressed as homodimers on the apical surface of choroid plexus epithelial cells. Mol Pharmacol 87(4):660–673
Hiramatsu M, Edamatsu R, Fujikawa N, Shirasu A, Yamamoto M, Suzuki S et al (1988) Measurement during convulsions of guanidino compound levels in cerebrospinal fluid collected with a catheter inserted into the cisterna magna of rabbits. Brain Res 455(1):38–42
Hise MA, Johanson CE (1979) The sink action of cerebrospinal fluid in uremia. Eur Neurol 18(5):328–337
Hladky SB, Barrand MA (2014) Mechanisms of fluid movement into, through and out of the brain: evaluation of the evidence. Fluids Barriers CNS 11(1):26
Hladky SB, Barrand MA (2016) Fluid and ion transfer across the blood-brain and blood-cerebrospinal fluid barriers; a comparative account of mechanisms and roles. Fluids Barriers CNS 13(1):19
Hosoya K, Tachikawa M (2011) Roles of organic anion/cation transporters at the blood-brain and blood-cerebrospinal fluid barriers involving uremic toxins. Clin Exp Nephrol 15(4):478–485
Hu Y, Shen H, Keep RF, Smith DE (2007) Peptide transporter 2 (PEPT2) expression in brain protects against 5-aminolevulinic acid neurotoxicity. J Neurochem 103(5):2058–2065
Huang JT, Wajda IJ (1977) The effects of morphine on the accumulation of homovanillic and 5-hydroxyindoleacetic acids in the choroid plexus of rats. Br J Pharmacol 60(3):363–367
Huang SL, Wang J, He XJ, Li ZF, Pu JN, Shi W (2014) Secretion of BDNF and GDNF from free and encapsulated choroid plexus epithelial cells. Neurosci Lett 566:42–45
Iliff JJ, Nedergaard M (2013) Is there a cerebral lymphatic system? Stroke 44(6 Suppl 1):S93–S95
Iliff JJ, Wang M, Liao Y, Plogg BA, Peng W, Gundersen GA et al (2012) A paravascular pathway facilitates CSF flow through the brain parenchyma and the clearance of interstitial solutes, including amyloid beta. Sci Transl Med 4(147):147ra11
Israel A, Garrido MR, Barbella Y, Becemberg I (1988) Rat atrial natriuretic peptide (99-126) stimulates guanylate cyclase activity in rat subfornical organ and choroid plexus. Brain Res Bull 20(2):253–256
Jacobs S, Ruusuvuori E, Sipila ST, Haapanen A, Damkier HH, Kurth I et al (2008) Mice with targeted Slc4a10 gene disruption have small brain ventricles and show reduced neuronal excitability. Proc Natl Acad Sci U S A 105(1):311–316
Janssen SF, van der Spek SJ, Ten Brink JB, Essing AH, Gorgels TG, van der Spek PJ et al (2013) Gene expression and functional annotation of the human and mouse choroid plexus epithelium. PLoS One 8(12):e83345
Jiang H, Hu Y, Keep RF, Smith DE (2009) Enhanced antinociceptive response to intracerebroventricular kyotorphin in Pept2 null mice. J Neurochem 109(5):1536–1543
Johanson CE (1984) Differential effects of acetazolamide, benzolamide and systemic acidosis on hydrogen and bicarbonate gradients across the apical and basolateral membranes of the choroid plexus. J Pharmacol Exp Ther 231(3):502–511
Johanson CE (1988) The choroid plexus-arachnoid-cerebrospinal fluid system. In: Boulton A, Baker G, Walz W (eds) Neuromethods: neuronal microenvironment- electrolytes and water spaces, vol 9. Humana, Clifton, NJ, pp 33–104
Johanson CE (2015) Fluid-forming functions of the choroid plexus: what is the role of aquaporin-1? In: Dorovini-Zis K (ed) The blood-brain barrier in health and disease, vol 1: Morphology, biology and immune function. CRC, Boca Raton, pp 140–171
Johanson CE (2017) Choroid plexus–cerebrospinal fluid transport dynamics: support of brain health and a role in neurotherapeutics. In: Conn PM (ed) Conn’s translational neuroscience. Elsevier, Academic, pp 233–261
Johanson C, Johanson N (2016) Merging transport data for choroid plexus with blood-brain barrier to model CNS homeostasis and disease more effectively. CNS Neurol Disord Drug Targets 15(9):1151–1180
Johanson C, Woodbury D (1974) Changes in CSF flow and extracellular space in the developing rat. In: Vernadakis A, Weiner N (eds) Drugs and the developing brain. Plenum, New York, pp 281–287
Johanson CE, Reed DJ, Woodbury DM (1974) Active transport of sodium and potassium by the choroid plexus of the rat. J Physiol 241(2):359–372
Johanson CE, Preston JE, Chodobski A, Stopa EG, Szmydynger-Chodobska J, McMillan PN (1999a) AVP V1 receptor-mediated decrease in cl- efflux and increase in dark cell number in choroid plexus epithelium. Am J Phys 276(1 Pt 1):C82–C90
Johanson CE, Szmydynger-Chodobska J, Chodobski A, Baird A, McMillan P, Stopa EG (1999b) Altered formation and bulk absorption of cerebrospinal fluid in FGF-2-induced hydrocephalus. Am J Phys 277(1 Pt 2):R263–R271
Johanson CE, Donahue JE, Spangenberger A, Stopa EG, Duncan JA, Sharma HS (2006) Atrial natriuretic peptide: its putative role in modulating the choroid plexus-CSF system for intracranial pressure regulation. Acta Neurochir Suppl 96:451–456
Johanson CE, Duncan JA III, Klinge PM, Brinker T, Stopa EG, Silverberg GD (2008) Multiplicity of cerebrospinal fluid functions: new challenges in health and disease. Cerebrospinal Fluid Res 5:10
Johanson CE, Stopa E, McMillan PN (2011a) The blood-cerebrospinal fluid barrier: structure and functional significance. Methods Mol Biol 686:101–131
Johanson CE, Stopa E, McMillan PN, Roth DR, Funk J, Krinke G (2011b) The distributional nexus of choroid plexus to CSF, ependyma and brain: toxicologic/pathologic phenomena, periventricular destabilization and lesion spread. Toxicol Pathol 39(1):186–212
Johanson C, Stopa E, Baird A, Sharma H (2011c) Traumatic brain injury and recovery mechanisms: peptide modulation of periventricular neurogenic regions by the choroid plexus-CSF nexus. J Neural Transm (Vienna) 118(1):115–133
Johanson CE, Stopa EG, Daiello L, de la Monte S, Keane M, Ott B (2018) Disrupted blood-CSF barrier to urea and creatinine in mild cognitive impairment and Alzheimer’s disease. J Alzheimers Dis Parkinsonism 8:2
Johnston M, Zakharov A, Koh L, Armstrong D (2005) Subarachnoid injection of microfil reveals connections between cerebrospinal fluid and nasal lymphatics in the non-human primate. Neuropathol Appl Neurobiol 31(6):632–640
Jones HC, Keep RF (1988) Brain fluid calcium concentration and response to acute hypercalcaemia during development in the rat. J Physiol 402:579–593
Kamal MA, Keep RF, Smith DE (2008) Role and relevance of PEPT2 in drug disposition, dynamics, and toxicity. Drug Metab Pharmacokinet 23(4):236–242
Kao L, Kurtz LM, Shao X, Papadopoulos MC, Liu L, Bok D et al (2011) Severe neurologic impairment in mice with targeted disruption of the electrogenic sodium bicarbonate cotransporter NBCe2 (Slc4a5 gene). J Biol Chem 286(37):32563–32574
Karimy JK, Zhang J, Kurland DB, Theriault BC, Duran D, Stokum JA et al (2017) Inflammation-dependent cerebrospinal fluid hypersecretion by the choroid plexus epithelium in posthemorrhagic hydrocephalus. Nat Med 23(8):997–1003
Keep RF, Jones HC (1990) A morphometric study on the development of the lateral ventricle choroid plexus, choroid plexus capillaries and ventricular ependyma in the rat. Brain Res 56(1):47–53
Keep RF, Smith DE (2011) Choroid plexus transport: gene deletion studies. Fluids Barriers CNS 8(1):26
Konsman JP, Tridon V, Dantzer R (2000) Diffusion and action of intracerebroventricularly injected interleukin-1 in the CNS. Neuroscience 101(4):957–967
Kunis G, Baruch K, Rosenzweig N, Kertser A, Miller O, Berkutzki T et al (2013) IFN-gamma-dependent activation of the brain’s choroid plexus for CNS immune surveillance and repair. Brain 136(Pt 11):3427–3440
Lam MA, Hemley SJ, Najafi E, Vella NGF, Bilston LE, Stoodley MA (2017) The ultrastructure of spinal cord perivascular spaces: implications for the circulation of cerebrospinal fluid. Sci Rep 7(1):12924
Lanz TA, Bove SE, Pilsmaker CD, Mariga A, Drummond EM, Cadelina GW et al (2012) Robust changes in expression of brain-derived neurotrophic factor (BDNF) mRNA and protein across the brain do not translate to detectable changes in BDNF levels in CSF or plasma. Biomarkers 17(6):524–531
Lee A, Anderson AR, Rayfield AJ, Stevens MG, Poronnik P, Meabon JS et al (2012) Localisation of novel forms of glutamate transporters and the cystine-glutamate antiporter in the choroid plexus: implications for CSF glutamate homeostasis. J Chem Neuroanat 43(1):64–75
Li Q, Ding Y, Krafft P, Wan W, Yan F, Wu G et al (2018) Targeting germinal matrix hemorrhage-induced overexpression of sodium-coupled bicarbonate exchanger reduces posthemorrhagic hydrocephalus formation in neonatal rats. J Am Heart Assoc 7(3):31
Lindvall M, Edvinsson L, Owman C (1977) Histochemical study on regional differences in the cholinergic nerve supply of the choroid plexus from various laboratory animals. Exp Neurol 55(1):152–159
Lindvall M, Edvinsson L, Owman C (1978a) Histochemical, ultrastructural, and functional evidence for a neurogenic control of CSF production from the choroid plexus. Adv Neurol 20:111–120
Lindvall M, Edvinsson L, Owman C (1978b) Sympathetic nervous control of cerebrospinal fluid production from the choroid plexus. Science (New York, NY) 201(4351):176–178
Lindvall M, Edvinsson L, Owman C (1978c) Reduced cerebrospinal fluid formation through cholinergic mechanisms. Neurosci Lett 10(3):311–316
Lippmann ES, Azarin SM, Kay JE, Nessler RA, Wilson HK, Al-Ahmad A et al (2012) Derivation of blood-brain barrier endothelial cells from human pluripotent stem cells. Nat Biotechnol 30(8):783–791
Lippmann ES, Al-Ahmad A, Azarin SM, Palecek SP, Shusta EV (2014) A retinoic acid-enhanced, multicellular human blood-brain barrier model derived from stem cell sources. Sci Rep 4:4160
Liszczak TM, Black PM, Foley L (1986) Arginine vasopressin causes morphological changes suggestive of fluid transport in rat choroid plexus epithelium. Cell Tissue Res 246(2):379–385
Lundgaard I, Lu ML, Yang E, Peng W, Mestre H, Hitomi E et al (2017) Glymphatic clearance controls state-dependent changes in brain lactate concentration. J Cereb Blood Flow Metab 37(6):2112–2124
MacAulay N, Zeuthen T (2010) Water transport between CNS compartments: contributions of aquaporins and cotransporters. Neuroscience 168(4):941–956
Majchrzak H, Kmieciak-Kołada K, Herman Z, Wencel T (1980) Homovanillic (HVA) and 5-hydroxyindoleacetic (5-HIAA) acid concentration in the cerebrospinal fluid of patients with supratentorial tumors and symptoms of intracranial hypertension (preliminary report). Neurol Neurochir Pol 14(1):87–90
Maktabi MA, Faraci FM (1994) Endogenous angiotensin II inhibits production of cerebrospinal fluid during posthypoxemic reoxygenation in the rabbit. Stroke 25(7):1489–1493. discussion 94
Maktabi MA, Heistad DD, Faraci FM (1991) Effects of central and intravascular angiotensin I and II on the choroid plexus. Am J Phys 261(5 Pt 2):R1126–R1132
Maktabi MA, Stachovic GC, Faraci FM (1993a) Angiotensin II decreases the rate of production of cerebrospinal fluid. Brain Res 606(1):44–49
Maktabi MA, Elbokl FF, Faraci FM, Todd MM (1993b) Halothane decreases the rate of production of cerebrospinal fluid. Possible role of vasopressin V1 receptors. Anesthesiology 78(1):72–82
Maren TH (1979) Effect of varying CO2 equilibria on rates of HCO3- formation in cerebrospinal fluid. J Appl Physiol Respir Environ Exerc Physiol 47(3):471–477
Maren TH (1988) The kinetics of HCO3- synthesis related to fluid secretion, pH control, and CO2 elimination. Annu Rev Physiol 50:695–717
Markey KA, Ottridge R, Mitchell JL, Rick C, Woolley R, Ives N et al (2017) Assessing the efficacy and safety of an 11beta-hydroxysteroid dehydrogenase type 1 inhibitor (AZD4017) in the idiopathic intracranial hypertension drug trial, IIH:DT: clinical methods and design for a phase II randomized controlled trial. JMIR Res Protoc 6(9):e181
Martin-de-Pablos A, Córdoba-Fernández A, Fernández-Espejo E (2018) Analysis of neurotrophic and antioxidant factors related to midbrain dopamine neuronal loss and brain inflammation in the cerebrospinal fluid of the elderly. Exp Gerontol 110:54–60
Marumo F, Masuda T, Masaki Y, Ando K (1988) The presence of atrial natriuretic peptide in canine cerebrospinal fluid and its possible origin in the brain. J Endocrinol 119(1):127–131
Masana M, Westerholz S, Kretzschmar A, Treccani G, Liebl C, Santarelli S et al (2018) Expression and glucocorticoid-dependent regulation of the stress-inducible protein DRR1 in the mouse adult brain. Brain Struct Funct 223:4039–4052
Michel CC, Mason JC, Curry FE, Tooke JE, Hunter PJ (1974) A development of the Landis technique for measuring the filtration coefficient of individual capillaries in the frog mesentery. Q J Exp Physiol Cogn Med Sci 59(4):283–309
Min-Chu L, Mackenna BR, Watt JA (1981) Evidence for the contribution by the cerebral cortex to 5-hydroxyindoleacetic acid found in the cerebrospinal fluid of cats. Brain Res 209(1):235–239
Mitro A, Lorencova M, Kutna V, Polak S (2018) Labelling of individual ependymal areas in lateral ventricles of human brain: ependymal tables. Bratisl Lek Listy 119(5):265–271
Mokgokong R, Wang S, Taylor CJ, Barrand MA, Hladky SB (2014) Ion transporters in brain endothelial cells that contribute to formation of brain interstitial fluid. Pflugers Arch 466(5):887–901
Mori K, Tsutsumi K, Kurihara M, Kawaguchi T, Niwa M (1990) Alteration of atrial natriuretic peptide receptors in the choroid plexus of rats with induced or congenital hydrocephalus. Childs Nerv Syst 6(4):190–193
Mudò G, Bonomo A, Di Liberto V, Frinchi M, Fuxe K, Belluardo N (2009) The FGF-2/FGFRs neurotrophic system promotes neurogenesis in the adult brain. J Neural Transm (Vienna) 116(8):995–1005
Murphy VA, Johanson CE (1989a) Acidosis, acetazolamide, and amiloride: effects on 22Na transfer across the blood-brain and blood-CSF barriers. J Neurochem 52(4):1058–1063
Murphy VA, Johanson CE (1989b) Alteration of sodium transport by the choroid plexus with amiloride. Biochim Biophys Acta 979(2):187–192
Murphy VA, Smith QR, Rapoport SI (1989) Uptake and concentrations of calcium in rat choroid plexus during chronic hypo- and hypercalcemia. Brain Res 484(1–2):65–70
Myung J, Wu D, Simonneaux V, Lane TJ (2018) Strong circadian rhythms in the choroid plexus: implications for sleep-independent brain metabolite clearance. J Exp Neurosci 12:1179069518783762
Nabeka H, Saito S, Li X, Shimokawa T, Khan MSI, Yamamiya K et al (2017) Interneurons secrete prosaposin, a neurotrophic factor, to attenuate kainic acid-induced neurotoxicity. IBRO Rep 3:17–32
Nagra G, Koh L, Zakharov A, Armstrong D, Johnston M (2006) Quantification of cerebrospinal fluid transport across the cribriform plate into lymphatics in rats. Am J Physiol Regul Integr Comp Physiol 291(5):R1383–R1389
Nakada T, Kwee IL (2019) Fluid dynamics inside the brain barrier: current concept of interstitial flow, glymphatic flow, and cerebrospinal fluid circulation in the brain. Neuroscientist 25(2):155–166
Nakamura S, Maeda K, Sasaki J, Tsubokawa T (1985) Serotonergic effect on cerebrospinal fluid production. No to Shinkei = Brain Nerve 37(3):237–242
Napoleone P, Sancesario G, Amenta F (1982) Indoleaminergic innervation of rat choroid plexus: a fluorescence histochemical study. Neurosci Lett 34(2):143–147
Naz N, Jimenez AR, Sanjuan-Vilaplana A, Gurney M, Miyan J (2016) Neonatal hydrocephalus is a result of a block in folate handling and metabolism involving 10-formyltetrahydrofolate dehydrogenase. J Neurochem 138(4):610–623
Nilsson C, Lindvall-Axelsson M, Owman C (1992) Neuroendocrine regulatory mechanisms in the choroid plexus-cerebrospinal fluid system. Brain Res Brain Res Rev 17(2):109–138
Nilsson C, Stahlberg F, Gideon P, Thomsen C, Henriksen O (1994) The nocturnal increase in human cerebrospinal fluid production is inhibited by a beta 1-receptor antagonist. Am J Phys 267(6 Pt 2):R1445–R1448
Nixon PF (2008) Glutamate export at the choroid plexus in health, thiamin deficiency, and ethanol intoxication: review and hypothesis. Alcohol Clin Exp Res 32(8):1339–1349
O’Donnell ME (2014) Blood-brain barrier Na transporters in ischemic stroke. Advances in pharmacology (San Diego). CAL 71:113–146
Ocrant I, Parmelee JT (1992) Immunofluorescent cytometry and electron microscopic immunolocalization of insulin-like growth factor (IGF)-II receptors in infant rat choroid plexus. Mol Cell Neurosci 3(4):354–359
Oldendorf WH, Davson H (1967) Brain extracellular space and the sink action of cerebrospinal fluid. Measurement of rabbit brain extracellular space using sucrose labeled with carbon 14. Arch Neurol 17(2):196–205
Oreskovic D, Klarica M (2010) The formation of cerebrospinal fluid: nearly a hundred years of interpretations and misinterpretations. Brain Res Rev 64(2):241–262
Oreskovic D, Klarica M (2014) A new look at cerebrospinal fluid movement. Fluids Barriers CNS 11:16
Oshio K, Song Y, Verkman AS, Manley GT (2003) Aquaporin-1 deletion reduces osmotic water permeability and cerebrospinal fluid production. Acta Neurochir Suppl 86:525–528
Palacios JM (2016) Serotonin receptors in brain revisited. Brain Res 1645:46–49
Palm DE, Knuckey NW, Primiano MJ, Spangenberger AG, Johanson CE (1995) Cystatin C, a protease inhibitor, in degenerating rat hippocampal neurons following transient forebrain ischemia. Brain Res 691(1–2):1–8
Pandey GN, Dwivedi Y, Ren X, Rizavi HS, Faludi G, Sarosi A et al (2006) Regional distribution and relative abundance of serotonin(2c) receptors in human brain: effect of suicide. Neurochem Res 31(2):167–176
Pappenheimer J, Heisey S, Jordan E (1961) Active transport of diodrast and phenolsulfonphthalein from cerebrospinal fluid to blood. Am J Phys 200:1–10
Parmelee JT, Johanson CE (1989) Development of potassium transport capability by choroid plexus of infant rats. Am J Phys 256(3 Pt 2):R786–R791
Paulson OB, Hertz MM, Bolwig TG, Lassen NA (1977) Filtration and diffusion of water across the blood-brain barrier in man. Microvasc Res 13(1):113–124
Pirttila TJ, Lukasiuk K, Hakansson K, Grubb A, Abrahamson M, Pitkanen A (2005) Cystatin C modulates neurodegeneration and neurogenesis following status epilepticus in mouse. Neurobiol Dis 20(2):241–253
Pollay M, Curl F (1967) Secretion of cerebrospinal fluid by the ventricular ependyma of the rabbit. Am J Phys 213(4):1031–1038
Praetorius J, Damkier HH (2017) Transport across the choroid plexus epithelium. Am J Physiol 312(6):C673–CC86
Praetorius J, Nielsen S (2006) Distribution of sodium transporters and aquaporin-1 in the human choroid plexus. Am J Physiol 291(1):C59–C67
Pullen RG, DePasquale M, Cserr HF (1987) Bulk flow of cerebrospinal fluid into brain in response to acute hyperosmolality. Am J Phys 253(3 Pt 2):F538–F545
Quintela T, Sousa C, Patriarca FM, Goncalves I, Santos CR (2015) Gender associated circadian oscillations of the clock genes in rat choroid plexus. Brain Struct Funct 220(3):1251–1262
Quintela T, Albuquerque T, Lundkvist G, Carmine Belin A, Talhada D, Gonçalves I et al (2018) The choroid plexus harbors a circadian oscillator modulated by estrogens. Chronobiol Int 35(2):270–279
Raha-Chowdhury R, Raha AA, Forostyak S, Zhao JW, Stott SR, Bomford A (2015) Expression and cellular localization of hepcidin mRNA and protein in normal rat brain. BMC Neurosci 16:24
Rall DP (1968) Transport through the ependymal linings. Prog Brain Res 29:159–172
Reed DJ, Yen MH (1978) The role of the cat choroid plexus in regulating cerebrospinal fluid magnesium. J Physiol 281:477–485
Saavedra JM, Kurihara M (1991) Autoradiography of atrial natriuretic peptide (ANP) receptors in the rat brain. Can J Physiol Pharmacol 69(10):1567–1575
Savolainen M, Emerich D, Kordower JH (2018) Disease modification through trophic factor delivery. Methods Mol Biol 1780:525–547
Schmitt C, Strazielle N, Richaud P, Bouron A, Ghersi-Egea JF (2011) Active transport at the blood-CSF barrier contributes to manganese influx into the brain. J Neurochem 117(4):747–756
Schultz WJ, Brownfield MS, Kozlowski GP (1977) The hypothalamo-choroidal tract. II. Ultrastructural response of the choroid plexus to vasopressin. Cell Tissue Res 178(1):129–141
Schwartz M, Baruch K (2014) The resolution of neuroinflammation in neurodegeneration: leukocyte recruitment via the choroid plexus. EMBO J 33(1):7–22
Schwartz M, Deczkowska A (2016) Neurological disease as a failure of brain-immune crosstalk: the multiple faces of neuroinflammation. Trends Immunol 37(10):668–679
Sharma HS, Johanson CE (2007) Intracerebroventricularly administered neurotrophins attenuate blood cerebrospinal fluid barrier breakdown and brain pathology following whole-body hyperthermia: an experimental study in the rat using biochemical and morphological approaches. Ann N Y Acad Sci 1122:112–129
Shechter R, Miller O, Yovel G, Rosenzweig N, London A, Ruckh J et al (2013) Recruitment of beneficial M2 macrophages to injured spinal cord is orchestrated by remote brain choroid plexus. Immunity 38(3):555–569
Shruthi S, Sumitha R, Varghese AM, Ashok S, Chandrasekhar Sagar BK, Sathyaprabha TN et al (2017) Brain-derived neurotrophic factor facilitates functional recovery from ALS-cerebral spinal fluid-induced neurodegenerative changes in the NSC-34 motor neuron cell line. Neurodegener Dis 17(1):44–58
Silverberg GD, Heit G, Huhn S, Jaffe RA, Chang SD, Bronte-Stewart H et al (2001) The cerebrospinal fluid production rate is reduced in dementia of the Alzheimer’s type. Neurology 57(10):1763–1766
Sinclair AJ, Onyimba CU, Khosla P, Vijapurapu N, Tomlinson JW, Burdon MA et al (2007) Corticosteroids, 11beta-hydroxysteroid dehydrogenase isozymes and the rabbit choroid plexus. J Neuroendocrinol 19(8):614–620
Smith SV, Friedman DI (2017) The idiopathic intracranial hypertension treatment trial: a review of the outcomes. Headache 57(8):1303–1310
Smith AJ, Verkman AS (2018) The “glymphatic” mechanism for solute clearance in Alzheimer’s disease: game changer or unproven speculation? FASEB J 32(2):543–551
Snodgrass SR, Johanson CE (2018) Choroid plexus: source of cerebrospinal fluid and regulator of brain development and function. In: Cinalli G (ed) Pediatric hydrocephalus. Springer, Berlin, pp 1–36
Sorensen SC, Gjerris F (1977) Adaptation of intraventricular pressure to acute changes in brain volume. Exp Eye Res 25(Suppl):387–390
Sørensen E, Olesen J, Rask-Madsen J, Rask-Andersen H (1978) The electrical potential difference and impedance between CSF and blood in unanesthetized man. Scand J Clin Lab Invest 38(3):203–207
Spector R, Johanson CE (1989) The mammalian choroid plexus. Sci Am 261(5):68–74
Spector R, Johanson CE (2014) The nexus of vitamin homeostasis and DNA synthesis and modification in mammalian brain. Mol Brain 7:3
Spector R, Keep RF, Snodgrass SR, Smith QR, Johanson CE (2015a) A balanced view of choroid plexus structure and function: focus on adult humans. Exp Neurol 267:78–86
Spector R, Snodgrass SR, Johanson CE (2015b) A balanced view of the cerebrospinal fluid composition and functions: focus on adult humans. Exp Neurol 273:57–68
Steardo L, Nathanson JA (1987) Brain barrier tissues: end organs for atriopeptins. Science (New York, NY) 235(4787):470–473
Steffensen AB, Oernbo EK, Stoica A, Gerkau NJ, Barbuskaite D, Tritsaris K et al (2018) Cotransporter-mediated water transport underlying cerebrospinal fluid formation. Nat Commun 9(1):2167
Stieger B, Gao B (2015) Drug transporters in the central nervous system. Clin Pharmacokinet 54(3):225–242
Stopa EG, Tanis KQ, Miller MC, Nikonova EV, Podtelezhnikov AA, Finney EM et al (2018) Comparative transcriptomics of choroid plexus in Alzheimer’s disease, frontotemporal dementia and Huntington’s disease: implications for CSF homeostasis. Fluids Barriers CNS 15(1):18
Szmydynger-Chodobska J, Chodobski A (2005) Peptide-mediated regulation of CSF formation and blood flow to the choroid plexus. In: Zheng W, Chodobski A (eds) The blood-cerebrospinal fluid barrier. CRC/Francis & Taylor Group, Boca Raton, FL, pp 101–117
Szmydynger-Chodobska J, Monfils PR, Lin AY, Rahman MP, Johanson CE, Chodobski A (1996) NADPH-diaphorase histochemistry of rat choroid plexus blood vessels and epithelium. Neurosci Lett 208(3):179–182
Szmydynger-Chodobska J, Chung I, Chodobski A (2006) Chronic hypernatremia increases the expression of vasopressin and voltage-gated Na channels in the rat choroid plexus. Neuroendocrinology 84(5):339–345
Tachikawa M, Hosoya K (2011) Transport characteristics of guanidino compounds at the blood-brain barrier and blood-cerebrospinal fluid barrier: relevance to neural disorders. Fluids Barriers CNS 8(1):13
Timmusk T, Mudò G, Metsis M, Belluardo N (1995) Expression of mRNAs for neurotrophins and their receptors in the rat choroid plexus and dura mater. Neuroreport 6(15):1997–2000
Tucker VL, Huxley VH (1990) Evidence for cholinergic regulation of microvessel hydraulic conductance during tissue hypoxia. Circ Res 66(2):517–524
Tulassay T, Khoor A, Bald M, Ritvay J, Szabo A, Rascher W (1990) Cerebrospinal fluid concentrations of atrial natriuretic peptide in children. Acta Paediatr Hung 30(2):201–207
Uchida Y, Zhang Z, Tachikawa M, Terasaki T (2015) Quantitative targeted absolute proteomics of rat blood-cerebrospinal fluid barrier transporters: comparison with a human specimen. J Neurochem 134(6):1104–1115
Uldall M, Botfield H, Jansen-Olesen I, Sinclair A, Jensen R (2017) Acetazolamide lowers intracranial pressure and modulates the cerebrospinal fluid secretion pathway in healthy rats. Neurosci Lett 645:33–39
Vemula S, Roder KE, Yang T, Bhat GJ, Thekkumkara TJ, Abbruscato TJ (2009) A functional role for sodium-dependent glucose transport across the blood-brain barrier during oxygen glucose deprivation. J Pharmacol Exp Ther 328(2):487–495
Vieira M, Gomes JR, Saraiva MJ (2015) Transthyretin induces insulin-like growth factor I nuclear translocation regulating its levels in the hippocampus. Mol Neurobiol 51(3):1468–1479
Vindedal GF, Thoren AE, Jensen V, Klungland A, Zhang Y, Holtzman MJ et al (2016) Removal of aquaporin-4 from glial and ependymal membranes causes brain water accumulation. Mol Cell Neurosci 77:47–52
Vogh BP, Godman DR (1989) Effects of inhibition of angiotensin converting enzyme and carbonic anhydrase on fluid production by ciliary process, choroid plexus, and pancreas. J Ocul Pharmacol 5(4):303–311
Wallingford MC, Chia JJ, Leaf EM, Borgeia S, Chavkin NW, Sawangmake C et al (2017) SLC20A2 deficiency in mice leads to elevated phosphate levels in cerebrospinal fluid and glymphatic pathway-associated arteriolar calcification, and recapitulates human idiopathic basal ganglia calcification. Brain Pathol 27(1):64–76
Walter HJ, Berry M, Hill DJ, Cwyfan-Hughes S, Holly JM, Logan A (1999) Distinct sites of insulin-like growth factor (IGF)-II expression and localization in lesioned rat brain: possible roles of IGF binding proteins (IGFBPs) in the mediation of IGF-II activity. Endocrinology 140(1):520–532
Wang D, Nykanen M, Yang N, Winlaw D, North K, Verkman AS et al (2011) Altered cellular localization of aquaporin-1 in experimental hydrocephalus in mice and reduced ventriculomegaly in aquaporin-1 deficiency. Mol Cell Neurosci 46(1):318–324
Weaver C, McMillan P, Duncan JA, Stopa E, Johanson C (2004) Hydrocephalus disorders: their biophysical and neuroendocrine impact on the choroid plexus epithelium. In: Hertz L (ed) Non-neuronal cells of the nervous system: function and dysfunction, vol 31. Elsevier, Amsterdam, pp 269–293
Welch K (1963) Secretion of cerebrospinal fluid by choroid plexus of the rabbit. Am J Phys 205:617–624
Woodard GE, Rosado JA (2008) Natriuretic peptides in vascular physiology and pathology. Int Rev Cell Mol Biol 268:59–93
Xiang J, Routhe LJ, Wilkinson DA, Hua Y, Moos T, Xi G et al (2017) The choroid plexus as a site of damage in hemorrhagic and ischemic stroke and its role in responding to injury. Fluids Barriers CNS 14(1):8
Xie L, Kang H, Xu Q, Chen MJ, Liao Y, Thiyagarajan M et al (2013) Sleep drives metabolite clearance from the adult brain. Science (New York, NY) 342(6156):373–377
Xu M, Xiao M, Li S, Yang B (2017) Aquaporins in nervous system. Adv Exp Med Biol 969:81–103
Yamasaki H, Sugino M, Ohsawa N (1997) Possible regulation of intracranial pressure by human atrial natriuretic peptide in cerebrospinal fluid. Eur Neurol 38(2):88–93
Zarebkohan A, Javan M, Satarian L, Ahmadiani A (2009) Effect of chronic administration of morphine on the gene expression level of sodium-dependent vitamin C transporters in rat hippocampus and lumbar spinal cord. J Mol Neurosci 38(3):236–242
Zeitzer JM, Maidment NT, Behnke EJ, Ackerson LC, Fried I, Engel J et al (2002) Ultradian sleep-cycle variation of serotonin in the human lateral ventricle. Neurology 59(8):1272–1274
Zemo DA, McCabe JT (2001) Salt-loading increases vasopressin and vasopressin 1b receptor mRNA in the hypothalamus and choroid plexus. Neuropeptides 35(3–4):181–188
Zeuthen T, Macaulay N (2012) Cotransport of water by Na(+)-K(+)-2Cl(−) cotransporters expressed in Xenopus oocytes: NKCC1 versus NKCC2. J Physiol 590(5):1139–1154
Zeuthen T, Gorraitz E, Her K, Wright EM, Loo DD (2016) Structural and functional significance of water permeation through cotransporters. Proc Natl Acad Sci U S A 113(44):E6887–E6e94
Zhang Z, Tachikawa M, Uchida Y, Terasaki T (2018) Drug clearance from cerebrospinal fluid mediated by organic anion transporters 1 (Slc22a6) and 3 (Slc22a8) at arachnoid membrane of rats. Mol Pharm 15(3):911–922
Zhao H, Yang H, Yan L, Jiang S, Xue L, Guan W et al (2014) Effects of lead exposure on copper and copper transporters in choroid plexus of rats. Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi 32(11):819–822
Zheng W (2005) Blood-CSF barrier in iron regulation and manganese-induced parkinsonism. In: Zheng W, Chodobski A (eds) The blood-cerebrospinal fluid barrier. CRC/Taylor and Francis, Boca Raton, FL
Zheng G, Chen J, Zheng W (2012) Relative contribution of CTR1 and DMT1 in copper transport by the blood-CSF barrier: implication in manganese-induced neurotoxicity. Toxicol Appl Pharmacol 260(3):285–293
Acknowledgments
This study was supported by grants to RFK: NS-093399, and NS-106746 from the National Institutes of Health (NIH). NIH funding to CEJ, as NS-27601 and NIA-AG027910, helped to produce some of the information and concepts in this chapter.
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Johanson, C.E., Keep, R.F. (2020). Blending Established and New Perspectives on Choroid Plexus-CSF Dynamics. In: Praetorius, J., Blazer-Yost, B., Damkier, H. (eds) Role of the Choroid Plexus in Health and Disease. Physiology in Health and Disease. Springer, New York, NY. https://doi.org/10.1007/978-1-0716-0536-3_2
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