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J Physiol. 1970 Jul; 209(1): 131–153.
PMCID: PMC1396036
PMID: 5499038

The effects of some inhibitors and accelerators of sodium transport on the turnover of 22Na in the cerebrospinal fluid and the brain

Abstract

1. The purpose of the experiments was to discover whether the turnover of 22Na in the c.s.f., which is largely determined by its rate of secretion, is affected in the same manner by inhibitors or accelerators of active transport as the turnover in the brain tissue since there is reason to believe that the composition of the extracellular fluid of brain is controlled by active processes.

2. Although acetazolamide (Diamox) inhibits rate of secretion of c.s.f. and the turnover of 22Na in this fluid it does not appreciably affect the turnover of 22Na in the brain tissue of either rat or rabbit, the small inhibition observed being probably secondary to the effects on the c.s.f.

3. Ouabain inhibits secretion of c.s.f. and turnover of 22Na in this fluid, but it, also, has no effect on turnover of 22Na in the brain tissue alone or in combination with Diamox.

4. Amphotericin B and amiloride, the anti-aldosterone spirolactone S.C. 114266, all inhibited secretion of c.s.f. without affecting turnover of 22Na in the brain tissue; actinomycin D, puromycin and cycloheximide, however, had no effect on secretion of c.s.f.

5. Vasopressin inhibited secretion of c.s.f. and turnover of 22Na in this fluid but increased the turnover in the brain by some 16%.

6. In the ventriculo—cisternally perfused rabbit, replacement of 80% of the NaCl in the perfusion fluid by choline chloride caused a slowing of the passage of 22Na from blood into the perfusion fluid.

7. On the basis of these results it is concluded that the brain extracellular fluid is not renewed by appreciable bulk-flow, in contrast with the c.s.f.

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Selected References

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  • Bentley PJ. Amiloride: a potent inhibitor of sodium transport across the toad bladder. J Physiol. 1968 Mar;195(2):317–330. [PMC free article] [PubMed] [Google Scholar]
  • BERING EA, Jr, SATO O. HYDROCEPHALUS: CHANGES IN FORMATION AND ABSORPTION OF CEREBROSPINAL FLUID WITHIN THE CEREBRAL VENTRICLES. J Neurosurg. 1963 Dec;20:1050–1063. [PubMed] [Google Scholar]
  • Bito LZ, Davson H. Local variations in cerebrospinal fluid composition and its relationship to the composition of the extracellular fluid of the cortex. Exp Neurol. 1966 Mar;14(3):264–280. [PubMed] [Google Scholar]
  • Brzezinski J, Kjällquist A, Siesjö BK. Mean carbon dioxide tension in the brain after carbonic anhydrase inhibition. J Physiol. 1967 Jan;188(1):13–23. [PMC free article] [PubMed] [Google Scholar]
  • Cameron IR, Davson H, Segal MB. The effect of hypercapnia on the blood-brain barrier to sucrose in the rabbit. Yale J Biol Med. 1969 Dec;42(3-4):241–247. [PMC free article] [PubMed] [Google Scholar]
  • Clark JM, Jr, Chang AY. Inhibitors of the transfer of amino acids from aminoacyl soluble ribonucleic acid to proteins. J Biol Chem. 1965 Dec;240(12):4734–4739. [PubMed] [Google Scholar]
  • Cohen MW, Gerschenfeld HM, Kuffler SW. Ionic environment of neurones and glial cells in the brain of an amphibian. J Physiol. 1968 Jul;197(2):363–380. [PMC free article] [PubMed] [Google Scholar]
  • CRABBE J, DEWEER P. ACTION OF ALDOSTERONE ON THE BLADDER AND SKIN OF THE TOAD. Nature. 1964 Apr 18;202:298–299. [PubMed] [Google Scholar]
  • Cutler RW, Barlow CF. The effect of hypercapnia on brain permeability to protein. Arch Neurol. 1966 Jan;14(1):54–63. [PubMed] [Google Scholar]
  • DAVSON H. A comparative study of the aqueous humour and cerebrospinal fluid in the rabbit. J Physiol. 1955 Jul 28;129(1):111–133. [PMC free article] [PubMed] [Google Scholar]
  • DAVSON H, LUCK CP. The effect of acetazoleamide on the chemical composition of the aqueous humour and cerebrospinal fluid of some mammalian species and on the rate of turnover of 24Na in these fluids. J Physiol. 1957 Jul 11;137(2):279–293. [PMC free article] [PubMed] [Google Scholar]
  • DAVSON H, POLLAY M. The turnover of 24Na in the cerebrospinal fluid and its bearing on the blood-brain barrier. J Physiol. 1963 Jul;167:247–255. [PMC free article] [PubMed] [Google Scholar]
  • DAVSON H, SPAZIANI E. The blood-brain barrier and the extracellular space of brain. J Physiol. 1959 Dec;149:135–143. [PMC free article] [PubMed] [Google Scholar]
  • Domer FR. Effects of diuretics on cerebrospinal fluid formation and potassium movement. Exp Neurol. 1969 May;24(1):54–64. [PubMed] [Google Scholar]
  • FISHMAN RA. Factors influencing the exchange of sodium between plasma and cerebrospinal fluid. J Clin Invest. 1959 Oct;38:1698–1708. [PMC free article] [PubMed] [Google Scholar]
  • Keilin D, Mann T. Carbonic anhydrase. Purification and nature of the enzyme. Biochem J. 1940 Sep;34(8-9):1163–1176. [PMC free article] [PubMed] [Google Scholar]
  • KOCH A, WOODBURY DM. Carbonic anhydrase inhibition and brain electrolyte composition. Am J Physiol. 1960 Feb;198:434–440. [PubMed] [Google Scholar]
  • Levine M, Oxender DL, Stein WD. The substrate-facilitated transport of the glucose carrier across the human erythrocyte membrane. Biochim Biophys Acta. 1965 Sep 27;109(1):151–163. [PubMed] [Google Scholar]
  • LICHTENSTEIN NS, LEAF A. EFFECT OF AMPHOTERICIN B ON THE PERMEABILITY OF THE TOAD BLADDER. J Clin Invest. 1965 Aug;44:1328–1342. [PMC free article] [PubMed] [Google Scholar]
  • Maren TH. Carbonic anhydrase: chemistry, physiology, and inhibition. Physiol Rev. 1967 Oct;47(4):595–781. [PubMed] [Google Scholar]
  • Oldendorf WH, Davson H. Brain extracellular space and the sink action of cerebrospinal fluid. Measurement of rabbit brain extracellular space using sucrose labeled with carbon 14. Arch Neurol. 1967 Aug;17(2):196–205. [PubMed] [Google Scholar]
  • PAPPENHEIMER JR, FENCL V, HEISEY SR, HELD D. ROLE OF CEREBRAL FLUIDS IN CONTROL OF RESPIRATION AS STUDIED IN UNANESTHETIZED GOATS. Am J Physiol. 1965 Mar;208:436–450. [PubMed] [Google Scholar]
  • Philpot FJ, Philpot JS. A modified colorimetric estimation of carbonic anhydrase. Biochem J. 1936 Dec;30(12):2191–2193. [PMC free article] [PubMed] [Google Scholar]
  • Pollay M, Curl F. Secretion of cerebrospinal fluid by the ventricular ependyma of the rabbit. Am J Physiol. 1967 Oct;213(4):1031–1038. [PubMed] [Google Scholar]
  • POLLAY M, DAVSON H. The passage of certain substances out of the cerebrosphinal fluid. Brain. 1963 Mar;86:137–150. [PubMed] [Google Scholar]
  • Reese TS, Karnovsky MJ. Fine structural localization of a blood-brain barrier to exogenous peroxidase. J Cell Biol. 1967 Jul;34(1):207–217. [PMC free article] [PubMed] [Google Scholar]
  • Welch K, Sadler K, Gold G. Volume flow across choroidal ependyma of the rabbit. Am J Physiol. 1966 Feb;210(2):232–236. [PubMed] [Google Scholar]

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