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惊厥后不同时间,对从大鼠多个脑区制备的脑片释放γ-氨基丁酸的抑制作用。

Inhibition of GABA release from slices prepared from several brain regions of rats at various times following a convulsion.

作者信息

Green A R, Minchin M C, Vincent N D

机构信息

MRC Clinical Pharmacology Unit, Radcliffe Infirmary, Oxford.

出版信息

Br J Pharmacol. 1987 Sep;92(1):13-8. doi: 10.1111/j.1476-5381.1987.tb11289.x.

Abstract

1 A method is described for the measurement of the K+-evoked release of endogenous gamma-aminobutyric acid (GABA) from slices of rat cortex, hippocampus and striatum. 2 In tissue prepared 30 min following an electroconvulsive shock, K+-evoked GABA release (above basal release) was inhibited by 45% in cortex, 50% in hippocampus and 75% in striatum. A similar inhibition of release was observed with slices prepared from rats in which a convulsion had been induced by flurothyl. There was no change in spontaneous (basal) release following either procedure. 3 An inhibition of K+-evoked endogenous GABA release was also seen in tissue prepared 4 min postictally but not 2 h after the seizure. 4 No difference was observed in the release of [3H]-GABA from preloaded cortical slices prepared from rats given a single electroconvulsive shock. 5 It is proposed that a convulsion results in an inhibition of GABA release and that this inhibition may in turn inhibit GABA synthesis as described in the preceding paper. 6 It is also proposed that changes in the endogenous releasable pool of GABA may not be detected by preloading slices with [3H]-GABA.

摘要
  1. 本文描述了一种测量大鼠皮层、海马体和纹状体切片中钾离子诱发内源性γ-氨基丁酸(GABA)释放的方法。2. 在电惊厥休克后30分钟制备的组织中,钾离子诱发的GABA释放(高于基础释放)在皮层中被抑制了45%,在海马体中被抑制了50%,在纹状体中被抑制了75%。在用氟烷诱发惊厥的大鼠制备的切片中也观察到了类似的释放抑制。两种处理后,自发性(基础)释放均无变化。3. 在发作后4分钟制备的组织中也观察到钾离子诱发的内源性GABA释放受到抑制,但在发作后2小时制备的组织中未观察到。4. 从接受单次电惊厥休克的大鼠制备的预加载皮层切片中,[3H]-GABA的释放没有差异。5. 有人提出,惊厥会导致GABA释放受到抑制,而这种抑制反过来可能会抑制GABA的合成,如前一篇论文所述。6. 还提出,用[3H]-GABA预加载切片可能检测不到内源性可释放GABA池的变化。

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The uptake of [3H]GABA by slices of rat cerebral cortex.大鼠大脑皮层切片对[3H]γ-氨基丁酸的摄取。
J Neurochem. 1968 Oct;15(10):1141-9. doi: 10.1111/j.1471-4159.1968.tb06831.x.

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