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组胺诱导大鼠大脑皮质切片释放去甲肾上腺素和5-羟色胺的机制研究。

Studies on the mechanism of histamine-induced release of noradrenaline and 5-hydroxytryptamine from slices of rat cerebral cortex.

作者信息

Young C S, Mason R, Hill S J

机构信息

Department of Physiology and Pharmacology, Medical School, Queen's Medical Centre, Nottingham, U.K.

出版信息

Biochem Pharmacol. 1988 Jul 15;37(14):2799-805. doi: 10.1016/0006-2952(88)90043-3.

Abstract

The effect of histamine on the release of endogenous noradrenaline and 5-hydroxytryptamine (5-HT) has been examined in slices of rat cerebral cortex. Histamine was found to produce a marked release of both amines from rat cerebral cortex at concentrations between 0.1 and 1 mM. This response to histamine was relatively resistant to removal of calcium ions from the incubation medium when compared to the release evoked by depolarising potassium stimuli. The response to 1 mM histamine was not, however, significantly inhibited by the H1-antagonist mepyramine (1 microM) or the H2-antagonist cimetidine (100 microM). Furthermore, impromidine which is both a potent H2-agonist and a potent H3-antagonist was without effect on the basal and histamine-stimulated release of endogenous noradrenaline and 5-HT. The response to histamine was, however, significantly attenuated by nisoxetine, fluoxetine and imipramine which are inhibitors of the amine uptake systems. The results of this study show that high concentrations (0.1 to 1 mM) of histamine can produce a marked increase in the release of endogenous 5-HT and noradrenaline from rat cerebral cortex, apparently via a non-receptor mechanism. This effect will need to be borne in mind in interpreting biochemical and behavioral responses to histamine in this concentration range.

摘要

已在大鼠大脑皮层切片中研究了组胺对内源性去甲肾上腺素和5-羟色胺(5-HT)释放的影响。发现组胺在0.1至1 mM的浓度下可使大鼠大脑皮层中的两种胺类物质显著释放。与去极化钾刺激所诱发的释放相比,这种对组胺的反应在去除孵育培养基中的钙离子后相对具有抗性。然而,1 mM组胺所引起的反应并未被H1拮抗剂美吡拉敏(1 microM)或H2拮抗剂西咪替丁(100 microM)显著抑制。此外,既是强效H2激动剂又是强效H3拮抗剂的英普咪定对内源性去甲肾上腺素和5-HT的基础释放及组胺刺激释放均无影响。然而,作为胺摄取系统抑制剂的尼索西汀、氟西汀和丙咪嗪可使对组胺的反应显著减弱。本研究结果表明,高浓度(0.1至1 mM)的组胺可使大鼠大脑皮层中内源性5-HT和去甲肾上腺素的释放显著增加,显然是通过一种非受体机制。在解释该浓度范围内对组胺的生化和行为反应时,需要牢记这一效应。

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