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5-羟色胺对大鼠离体输精管的直接和间接作用。

Direct and indirect actions of 5-hydroxytryptamine on the rat isolated vas deferens.

作者信息

Lucchelli A, Santagostino-Barbone M G, Modesto F, Grana E

出版信息

Arch Int Pharmacodyn Ther. 1984 Jun;269(2):236-51.

PMID:6433824
Abstract

The contractile effect of 5-hydroxytryptamine on the rat isolated vas deferens was analyzed. In tissues from reserpine-pretreated animals 5-hydroxytryptamine (1 X 10(-6) M-3 X 10(-4) M) induced effects which were much lower than those induced in tissues from normal animals; the effects of low and medium concentrations of 5-hydroxytryptamine were antagonized by methysergide, those of medium and high concentrations were inhibited by phentolamine. In tissues from normal animals 5-hydroxytryptamine-induced contractions were compared with those induced by noradrenaline. 5-Hydroxytryptamine was less potent than noradrenaline and exhibited tachyphylaxis when the time interval between two successive exposures was too short. Phentolamine and dihydroergocristine reduced the effects of 5-hydroxytryptamine at concentrations lower than those necessary to antagonize noradrenaline-induced effects. Methysergide only reduced the effects of lower concentrations of 5-hydroxytryptamine. Cross-protection experiments showed that when noradrenaline was added before dibenamine, responses to both 5-hydroxytryptamine and noradrenaline were maintained to a very similar degree, while when 5-hydroxytryptamine was used as a protecting agent only a small degree of protection was found both towards noradrenaline and 5-hydroxytryptamine-induced effects. Cocaine potentiated the effects of low concentrations of 5-hydroxytryptamine while inhibiting those of high concentrations. The present study provides direct and indirect evidences that the contractile effect of 5-hydroxytryptamine on the rat vas deferens is prevailingly due to the release of noradrenaline; in the lower part of the concentration-response curve also direct effects are involved which are mediated by an interaction with both tryptaminergic "D" receptors and alpha 1-adrenoceptors.

摘要

分析了5-羟色胺对大鼠离体输精管的收缩作用。在利血平预处理动物的组织中,5-羟色胺(1×10⁻⁶M - 3×10⁻⁴M)诱导的效应远低于正常动物组织中的效应;低、中浓度5-羟色胺的效应被甲基麦角新碱拮抗,中、高浓度的效应被酚妥拉明抑制。在正常动物的组织中,比较了5-羟色胺诱导的收缩与去甲肾上腺素诱导的收缩。5-羟色胺的效力低于去甲肾上腺素,并且当两次连续暴露之间的时间间隔过短时会出现快速耐受性。酚妥拉明和双氢麦角隐亭在低于拮抗去甲肾上腺素诱导效应所需的浓度下降低了5-羟色胺的效应。甲基麦角新碱仅降低较低浓度5-羟色胺的效应。交叉保护实验表明,当在二苄胺之前加入去甲肾上腺素时,对5-羟色胺和去甲肾上腺素的反应都能维持在非常相似的程度,而当使用5-羟色胺作为保护剂时,对去甲肾上腺素和5-羟色胺诱导的效应仅发现有很小程度的保护。可卡因增强了低浓度5-羟色胺的效应,同时抑制了高浓度的效应。本研究提供了直接和间接证据,表明5-羟色胺对大鼠输精管的收缩作用主要是由于去甲肾上腺素的释放;在浓度-反应曲线的较低部分也涉及直接效应,这些效应是由与色胺能“D”受体和α1-肾上腺素能受体的相互作用介导的。

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