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一种γ-氨基丁酸(GABA)受体结合的内源性抑制剂。

An endogenous inhibitor of GABA receptor binding.

作者信息

Kuroda H, Ogawa N, Nukina I, Ota Z

出版信息

Neurochem Res. 1984 Jan;9(1):21-7. doi: 10.1007/BF00967656.

Abstract

An endogenous inhibitor of GABA receptor binding was prepared from synaptic membrane of rat brain with 0.05% Triton X-100. The endogenous inhibitor was competitive with GABA for GABA binding sites. The inhibition of GABA receptor binding by the endogenous inhibitor was blocked by the allosteric effect of diazepam. In the presence of diazepam, specific [3H]GABA binding was greater in a medium containing the endogenous inhibitor than in one containing an equal inhibitory potency of GABA, whereas there was no difference in the absence of diazepam. This indicated that the endogenous inhibitor was not GABA itself.

摘要

用0.05%的曲拉通X-100从大鼠脑突触膜制备了一种γ-氨基丁酸(GABA)受体结合的内源性抑制剂。该内源性抑制剂与GABA竞争GABA结合位点。地西泮的变构效应可阻断内源性抑制剂对GABA受体结合的抑制作用。在地西泮存在的情况下,含有内源性抑制剂的培养基中特异性[3H]GABA结合比含有同等抑制效力GABA的培养基中更高,而在地西泮不存在时则没有差异。这表明内源性抑制剂不是GABA本身。

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