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H3受体控制人脑中组胺的释放。

H3-receptors control histamine release in human brain.

作者信息

Arrang J M, Devaux B, Chodkiewicz J P, Schwartz J C

机构信息

Unité 109 de Neurobiologie et Pharmacologie, Centre Paul Broca de l'INSERM, Paris, France.

出版信息

J Neurochem. 1988 Jul;51(1):105-8. doi: 10.1111/j.1471-4159.1988.tb04841.x.

Abstract

The regulation of histamine release was studied on slices prepared from pieces of human cerebral cortex removed during neurosurgery and labeled with L-[3H]histidine. Depolarization by increased extracellular K+ concentration induced [3H]histamine release, although to a lesser extent than from rat brain slices. Exogenous histamine reduced by up to 60% the K+-evoked release, with an EC50 of 3.5 +/- 0.5 X 10(-8) M. The H3-receptor antagonists impromidine and thioperamide reversed the histamine effect in an apparently competitive manner and enhanced the K+-evoked release, indicating a participation of endogenous histamine in the release control process. The potencies of histamine and the H3-receptor antagonists were similar to those of these agents at presynaptic H3-autoreceptors controlling [3H]histamine release from rat brain slices. It is concluded that H3-receptors control histamine release in the human brain.

摘要

利用神经外科手术中切除的人类大脑皮层组织切片,用L-[3H]组氨酸进行标记,研究了组胺释放的调节机制。细胞外钾离子浓度升高引起的去极化可诱导[3H]组胺释放,但其释放程度低于大鼠脑切片。外源性组胺可使钾离子诱发的释放减少高达60%,半数有效浓度(EC50)为3.5±0.5×10(-8)M。H3受体拮抗剂英普咪定和硫代哌酰胺以明显的竞争性方式逆转了组胺的作用,并增强了钾离子诱发的释放,表明内源性组胺参与了释放控制过程。组胺和H3受体拮抗剂的效力与这些药物在控制大鼠脑切片[3H]组胺释放的突触前H3自身受体上的效力相似。得出结论:H3受体控制人类大脑中的组胺释放。

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