Abstract
The physiological and pharmacological examination of the nervous system enjoyed enormous popularity over the last several decades It is now possible to record the electrical currents generated by ions passing through individual membrane channels and to define precisely the molecular characteristics of individual receptor aggregates Success in these endeavors has arisen, in part, from the use of sophisticated biochemical, electrophysiological, and pharmacological techniques, often carried out in isolated neural tissue. Despite the wealth of information generated by this approach to brain function, our knowledge of how the brain works as a whole to integrate and direct a basic physiological or behavioral drive is still scanty. The brain is well-endowed with putative neurotransmitter molecules whose functions are still unknown The utility of perfusion technology as a potent tool for addressing this problem is outlined in Table 1 and also has been pointed out previously (Myers, 1972) In this chapter, we will examine critically some of the theoretical and methodological issues raised in perfusing cerebral structures, and give descriptions of the methodology involved In view of space limitations, frequent reference to the literature will be made to assist the reader in obtaining precise descriptions of some of the techniques under discussion Of particular value is the 1972 chapter by Myers.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Arnold E B, Mohnoff P B, and Rutledge C O (1977). The release of endogenous norepinephrme and dopamme from cerebral cortex by amphetamine J Pharmacol Exp Ther 202, 544–557
Barthohni G, Stadler H, Gadea Ciria M., and Lloyd K. G. (1976) The use of the push-pull cannula to estimate the dynamics of acetylcholine and catecholamines within various brain areas. Neuropharmacology 15, 515–519
Battacharva B K and Feldberg W (1958). Perfusion of cerebral ventricles effects of drugs on outflow from the cisterna and aqueduct. Br J. Pharmacol 13, 156–162
Bayon A., Shoemaker W J., Lugo L., Azad R., Ling N, Drucker-Colin R. R, and Bloom F. E. (1981). In vivo release of enkephalin from the globus pallidus. Neurosa Lett. 24, 65–70.
Besson M J., Cheramy A, Feltz P., and Glowinski J. (1969) Release of newly synthesized dopamine from dopamine containing terminals in the stnatum of the rat. Proc. Natl Acad. Sci USA 62, 741–748
Besson M J., Cheramy A., Feltz P., and Glowmski J (1971). Dopamine spontaneous and drug-induced release from the caudate nucleus in the cat. Brain Res. 32, 407–424.
Bissonnette J M, Hohimer A R, and Richardson B. S. (1981) Ventriculocisternal cerebrospmal perfusion in unanesthetized fetal lambs J. Appl Physiol 50, 880–883
Bloom F. E and Giarman N J (1968) Physiologic and pharmacologic considerations of biogenic amines in the nervous system, Ann Rev Pharmacol. 8, 229–258
Bourque C. W. and Renaud L P. (1983). A perfused in vitro preparation of hypothalamus for electrophysiological studies on neurosecretory neurons J Neurosa Methods 7, 203–214
Carmichael E A, Feldberg W, and Fleischhauer K. (1964). Methods for perfusing different parts of the cat’s cerebral ventricles with drugs. J Physiol (Lond ) 173, 354–367.
Celesia G G and Jasper H H (1966) Acetylcholine released from cerebral cortex in relation to state of activation Neurology 16, 1053–1063
Chang T M., Passaro E Jr, Debas H, Yamada T., and Oldendorf W. H (1984). Influence of cisternal pressure on passage of neuropeptides from the cerebrospmal fluid into the peripheral circulation. Brain Res. 300, 172–174.
Chase, T N and Kopin, I J. (1968). Stimulus induced release of substances from the olfactory bulb using the push-pull cannula. Nature (Lond) 217, 466–467.
Chen J. C, Rhee K K, Beaudry D.M., and Ramirez, V D (1984) In vivo output of dopamine and metabolites from the rat caudate nucleus as estimated with push-pull perfusion on-line with HPLC-EC in unrestrained, conscious rats. Neuroendocnnology 38, 362–370
Cooper J. F., Hochstein H. D., and Sehgmann E. B. Jr (1972) The limulus test for endotoxin (pyrogen) in radiopharmaceuticals and biologicals Bull Parenter Drug Assoc 26, 153–162
Cooper K. E, Kasting, N W Ledens, K., and Veale, W. L (1979) Evidence supporting a role for vasopressin in natural suppression of fever in sheep J Physiol. (Lond ) 195, 33–45
Cooper K E. and Veale W. L. (1972) Exchange between the blood brain and cerebrospmal fluid of substances which can induce or modify febrile responses The Pharmacology of Thermoregulatwn Symposium, San Francisco, 277–288.
Davson H and Welch K (1971) The Relations of Blood, Brain and Cerebrospmal Fluid, in Ion Homeostasis of the Brain (siesjo, B K. and Sorensen, S C, eds. ), 9–21. Academic Press, New York
Delgado J. M R and Rubenstein L. (1964) Intracranial release of neurohumors in unanesthetized monkeys Arch Int Pharmacodyn Ther. 150, 530–546
Dingledine R, Dodd J, and Kelly J S. (1980) The in vitro brain slice as a useful neurophysiological preparation for intracellular recording J Neurosa Methods 2, 323–362
Elghozi J. L, Le Quan-Bm K H., Earnhardt J T, Meyer P and Devynck M A (1981) In vivo dopamine release from the anterior hypothalamus of the rat Eur J Pharmacol 73, 199–208
Fox R. H and Hilton S. M (1958) Bradykinm formation in human skin as a factor in heart vasodilatation J Physiol (Lond ) 142, 219–232
Feldberg W and Fleischhaur K (1960) Penetration of homo-phenol blue from the perfused cerebral ventricles into the brain tissue J Physiol (Lond ) 150, 451–462
Feldberg W., Myers R D, and Veale W. L (1970). Perfusion from cerebral ventricle to cisterna magna in the unanaesthetized cat Effect of calcium on body temperature J. Physiol (Lond ) 207, 403–416
Fuxe K and Ungerstedt U (1968) Histochemical studies on the distribution of catecholamines and 5-hydroxytryptamine after intraventricular injections Histochemie 13, 16–28
Gaddum J H (1961) Push-pull cannulae J Physiol (Lond ) 155, P1–P2
Hememann U, Lux H D, and Gutnick M J (1977) Extracellular free calcium and potassium during paroxysmal activity in the cerebral cortex of the cat Exp, Brain Res 27, 237–243
Hery F., Faudon M., and Ternaux J. P (1982). In vivo release of serotonin in two raphe nuclei (raphe dorsalis and magnus) of the cat Brain Res Bull 8, 123–129.
Honchar M. P, Hartman B K, and Sharpe L G (1979). Evaluation of in vivo brain site perfusion with the push-pull cannula Am J Physiol 236, R48–R56
Imperato A and Di Chiara G. (1984). Trans-stnatal dialysis coupled to reverse phase high performance liquid chromatography with electrochemical detection a new method for the study of the in vivo release of endogenous dopamine and metabolites Neurosci 4, 966–977
Izquierdo I and Izquierdo J A. (1971). Effects of drugs on deep brain centers Ann Rev Pharmacol 11, 189–208
Johnson R D and Justice J B (1983) Model studies for brain dialysis Brain Res Bull 10, 567–571
Jordan C. C and Webster R A (1978) The release of acetylcholine in the perfused cat spinal cord in vivo Neuropharmacology 17, 321–327
Kasting N W, Carr D. B, Martin J. B., Blume H, and Bergland R (1983) Changes in cerebrospinal fluid and plasma vasopressin in the febrile sheep Can J Physiol Pharmacol 61, 427–431
Leusen I (1950) The influence of calcium, potassium and magnesium ions in cerebrospmal fluid on vasomotor system J Physiol (Lond ) 110, 319–329
Levine J E and Ramirez V D (1980) In vivo release of lutemizing hormone-releasing hormone estimated with push-pull cannulae from the mediobasal hypothalami of ovanectomized, steroidprimed rats Endocrinology 107, 1782–1790
Llinas R., Yarom Y., and Sugimoru M. (1981). The isolated mammalian brain in vitro a new technique for the analysis of the electrical activity of neuronal circuit function. Fed Proc. 40, 2240–2245
Loullis C C, Hingtgen J. N, Shea P. A, and Aprison M H. (1980) In vivo determination of endogenous biogenic amines in rat brain using HPLC and push-pull cannula Pharmacol Biochem. Behav 12, 959–963
Malkinson T. J, Jackson-Middelkoop L. M, and Veale W L (1977). A simple multi-purpose cannula system for access to the brain and/or systemic vascular system of unanesthetized animals Brain Res Bull 2, 57–59
Martin G E and Myers R D (1975) Evoked release of [14C] norepinephrine from the rat hypothalamus during feeding. Am. J Physiol 229, 1547–1555
McIlwain H and Rodnight R (1962) Practical Neurochemistry, Churchill-Livingstone, London
Mitchell J F (1963). The spontaneous and evoked release of acetylcholine from the cerebral cortex J Physiol (Lond) 165, 98–116.
Moir A T B and Dow R C (1970) A simple method allowing perfusion of cerebral ventricles of the conscious rabbit J Appl Physiol 28, 528–529.
Morton I K. M Stagg C J. and Webster R. A (1977) Perfusion of the central canal and subarachnoid space of the cat and rabbit spinal cord in vivo. Neuropharmacology 16, 1–
Muhlethaler M, Sawyer W H., Manning M M, and Dreifuss J J (1983). Characterization of a uterine-type oxytocin receptor in the rat hippocampus Proc Natl Acad Sci USA 80, 6713–6717
Myers R. D (1970) An improved push-pull cannula system for perfusing an isolated region of the brain Physiol Behav 5, 243–246
Myers R. D. (1972). Methods for Perfusing Different Structures of the Brain, in Methods in Psychobiology vol 2, (R. D. Myers, ed) pp 169–211, Academic Press, New York.
Nieoullon A., Cheramy A, and Glowinski J (1977) An adaptation of the push-pull cannula method to study the in vivo release of [3H] dopamme synthesized from [3H]tyrosine in the cat caudate nucleus-effects of various physical and pharmacological treatments. J Neurochem 28, 819–828
Otsuka M and Konishi S. (1974) Electrophysiology of mammalian spinal cord in vitro. Nature (Lond ) 252, 733–734
Palfreyman M G, Huot S, and Grove J (1983). Total GABA and homocarnosme in CSF as indices of brain GABA concentrations Neurosa Lett 35, 161–166
Pappenheimer J. R., Heisey S. R., Jordan E F., and De Downer J (1962). Perfusion of the cerebral ventricular system in unanesthetized goats Am J. Physiol 203, 763–774
Philips S. R, Robson A. M, and Boulton A A. (1982). Unstimulated and amphetamine-stimulated release of endogenous noradrenaline and dopamine from rat brain in vivo J Neurochem 38, 1106–1110
Phillis, J. W. (1968) Acetylcholine release from the cerebral cortex its role in cortical arousal Brain Res 7, 378–389
Pierau F. R K., Klee M R., and Klussmann F W (1976) Effect of temperature on postsynaptic potentials of cat spinal motoneurones Brain Res 144, 21–34
Pittman Q. J, Hatton J. D., and Bloom F E (1980) Morphine and opioid peptides reduce paraventncular neuronal activity, studies on the rat hypothalamic slice preparation Proc Natl Acad. Sci USA 77, 5527–5531.
Pittman Q J, Lawrence D., and McLean L (1982) Central effects of arginine vasopressin on blood pressure in rats Endocrinology 110, 1058–1060.
Pittman Q J, Riphagen C L, and Ledens K (1984) Release of immunoassayable neurohypophyeal peptides from rat spinal cord, in vivo Brain Res 300, 321–326
Redgrave, Peter (1977) A modified push-pull system for the localised perfusion of brain tissue Pharmacol Bwchem Behav. 6, 471–474
Riddell D and Szerb J C (1971) The release in vivo of dopamine synthesized from labeled precursors in the caudate nucleus of the cat J Neurochem. 18, 989–1006
Robinson, I C A. F (1983). Neurohypophysial Peptides in the Cerebrospinal Fluid, in The Neumhypophysis Structure, Function and Control, Progress in Brain Research, vol. 60, (Cross B A and Lenz G, eds ), pp. 129–145, Elsevier, Amsterdam
Szerb J. C. (1967) Model experiments with Gaddum’s push-pull cannulas. Can. J Physiol Pharmacol 45, 613–620.
Tossman U. and Ungerstedt U (1981) Neuroleptic action on putative amino acid neurotransmitters in the brain studied with a new technique of brain dialysis Neurosci Lett. Suppl 7, S479
Van der Gugten J. and Slangen J L (1977). Release of endogenous catecholamines from rat hypothalamus in vivo related to feeding and other behaviors Pharmacol Bwchem Behav 7, 211–219.
Walton K. and Fulton B. (1983) Hydrogen peroxide as a source of molecular oxygen for in vitro mammalian CNS preparations Brain Res 278, 387–393
Wood J H. (1980) Physiology, Pharmacology and Dynamics of Cerebrospinal Fluid, in Neurobiology of Cerebrospinal Fluid, (Wood, J H ed.) pp. 1–16, Plenum Press, New York.
Yaksh T L. and Rudy T. A. (1976) Chronic catheterization of the spinal subarachnoid space Physiol Behav 17, 1031–1036
Yaksh T L and Tyce G M (1980) Resting and K +-evoked release of serotonin and norepinephrine in vivo from the rat and cat spinal cord Brain Res 192, 133–146.
Yaksh T. L. and Yamamura H. I (1974). Factors affecting performance of the push-pull cannula in brain J Appl Physiol 37, 428–434
Yamamoto C. (1972) Activation of hippocampal neurons by mossy fiber stimulation in thin brain sections in vitro Exp brain Res 14, 423–435
Zetterstrom T. and Ungerstedt U (1984). Effects of apomorphine on the in vivo release of dopamine and its metabolites, studied by brain dialysis Eur J Pharmacol 97, 29–36.
Zetterstrom T., Sharp T, Marsden C. A., and Ungerstedt U. (1983) In vivo measurement of dopamine and its metabolites by intracerebral dialysis: changes after d-amphetamine. J. Neurochem. 41, 1769–1773
Author information
Authors and Affiliations
Editor information
Rights and permissions
Copyright information
© 1985 The Humana Press Inc.
About this protocol
Cite this protocol
Plttman, Q.J., Dlsturnal, J., Rlphagen, C., Veale, W.L., Bauce, L. (1985). Perfusion Techniques for Neural Tissue. In: Boulton, A.A., Baker, G.B. (eds) General Neurochemical Techniques. Neuromethods, vol 1. Humana Press, Totowa, NJ. https://doi.org/10.1385/0-89603-075-x:279
Download citation
DOI: https://doi.org/10.1385/0-89603-075-x:279
Publisher Name: Humana Press, Totowa, NJ
Print ISBN: 978-0-89603-075-6
Online ISBN: 978-1-59259-606-5
eBook Packages: Springer Protocols