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[离体大鼠回肠对5-羟色胺反应中的收缩与舒张机制(作者译)]

[Mechanisms of contraction and relaxation in the response to 5'hydroxytriptamine of isolated rat ileum (author's transl)].

作者信息

Furukawa K

出版信息

Nihon Yakurigaku Zasshi. 1978 May;74(4):525-37.

PMID:700515
Abstract

The action of 5-hydroxytryptamine (5-HT) in the rat ileum was analysed pharmacologically. In the isolated rat ileum, either mono or biphasic contraction was induced depending on the concentrations of 5-HT. The former was induced by lower concentrations of 5-HT (less than 6.25 X 10(-7)M) and the latter by higher concentrations of 5-HT (greater than 2.5 X 10 (-6)M). The monophasic contraction and the tonic contraction in response to 5-HT were blocked by methysergide (MTG). The phasic contraction in response to 5-HT after inhibition of muscular receptor with MTG was potentiated by physostigmine and blocked by mecamylamine (MC) or tetrodo-toxin (TTX). The response to 5-HT changed from a contraction to a relaxation by preincubation with MTG plus hyoscine. The relaxation was inhibited by TTX but not by MC and such was provoked even in the ileum from rats treated with 6-hydroxydopamine. Therefore, the inhibitory neuronal receptor for 5-HT does not appear to belong to the adrenergic nervous system. At lower concentrations of 5-HT, relaxation was induced with MTG which was only partially inhibited by TTX. These results indicate that the stimulatory response to 5-HT were caused by activations of muscular receptors and of intramural parasympathetic ganglion cells while inhibitory responses were caused by activations of non-adrenergic inhibitory nerve terminals and of non-neuronal elements.

摘要

对5-羟色胺(5-HT)在大鼠回肠中的作用进行了药理学分析。在离体大鼠回肠中,根据5-HT的浓度可诱导单相或双相收缩。前者由较低浓度的5-HT(小于6.25×10⁻⁷M)诱导,后者由较高浓度的5-HT(大于2.5×10⁻⁶M)诱导。5-HT引起的单相收缩和强直性收缩被麦角新碱(MTG)阻断。用MTG抑制肌肉受体后,5-HT引起的相性收缩被毒扁豆碱增强,并被美加明(MC)或河豚毒素(TTX)阻断。预先用MTG加东莨菪碱孵育后,对5-HT的反应从收缩变为松弛。这种松弛被TTX抑制,但不被MC抑制,即使在经6-羟基多巴胺处理的大鼠回肠中也会出现这种情况。因此,5-HT的抑制性神经受体似乎不属于肾上腺素能神经系统。在较低浓度的5-HT作用下,MTG可诱导松弛,TTX只能部分抑制这种松弛。这些结果表明,对5-HT的刺激反应是由肌肉受体和壁内副交感神经节细胞的激活引起的,而抑制反应是由非肾上腺素能抑制性神经末梢和非神经元成分的激活引起的。

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