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The Effects in Vitro of Hypoglycaemia and Recovery from Anoxia on Synaptosomal Metabolism

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Journal Biochem J
Specialty Biochemistry
Date 1982 Sep 15
PMID 6816223
Citations 9
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Abstract

Synaptosomes from several regions of the rat brain were found to exhibit half-maximal rates of 14CO2 output and [14C]acetylcholine synthesis from D-[U-14C]glucose at glucose concentrations approx. 50-fold lower than those required by the brain in situ. However, synaptosomal acetylcholine synthesis was found not to be directly proportional to substrate oxidation as measured by 14CO2 output. When synaptosomes had been exposed to anoxia in vitro, their metabolic indices (14CO2 and [14C]acetylcholine synthesis, and adenine nucleotide levels) were found not to be significantly different from control aerobic values, unless they had been subjected to veratridine depolarization. This is in accord with previous findings that neither the absolute metabolic rates nor the vulnerability to hypoxic damage exhibited by brain in situ is reflected by brain slices in vitro, unless these are stimulated by depolarization. The use of synaptosomes as a model for synaptic damage in vivo is discussed.

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References
1.
Kovachich G . Depression of 14CO2 production from [U-14C] glucose in brain slices under high-pressure oxygen: relationship between metabolic rate and tissue sensitivity to oxygen. J Neurochem. 1980; 34(2):459-62. DOI: 10.1111/j.1471-4159.1980.tb06620.x. View

2.
Booth R, Clark J . A method for the rapid separation of soluble and particulate components of rat brain synaptosomes. FEBS Lett. 1979; 107(2):387-92. DOI: 10.1016/0014-5793(79)80414-7. View

3.
Ksiezak H, Gibson G . Acetylcholine synthesis and CO2 production from variously labeled glucose in rat brain slices and synaptosomes. J Neurochem. 1981; 37(1):88-94. DOI: 10.1111/j.1471-4159.1981.tb05294.x. View

4.
Fletcher A, Bachelard H . Demonstration of high affinity hexose uptake in cerebral cortex-slices. J Neurochem. 1978; 31(1):233-6. DOI: 10.1111/j.1471-4159.1978.tb12453.x. View

5.
Grewaal D, QUASTEL J . Control of synthesis and release of radioactive acetylcholine in brain slices from the rat. Effects of neurotropic drugs. Biochem J. 1973; 132(1):1-14. PMC: 1177553. DOI: 10.1042/bj1320001. View