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大鼠后肢5-羟色胺受体的某些特性

Some properties of 5-hydroxytryptamine receptors in the hindquarters of the rat.

作者信息

Cooper M, Wyllie J H

出版信息

Br J Pharmacol. 1979 Sep;67(1):79-85.

Abstract

1 The rat hindquarter preparation, as described, responds with reproducible vasoconstriction to noradrenaline and tryptamines. 2 The receptors involved in these responses are distinct. 3 Evidence of heterogeneity of tryptamine receptors was not obtained. 4 The 5-hydroxytryptamine (5-HT) antagonists, methysergide and cyproheptadine, although very potent, displayed antagonism of a non-competitive type whereas a series of phenothiazines and phentolamine displayed competitive antagonism against 5-HT. 5 For the phenothiazines the order of increasing potency was promazine less than chlorpromazine less than triflupromazine.

摘要
  1. 如所述,大鼠后肢标本对去甲肾上腺素和色胺会产生可重复的血管收缩反应。2. 参与这些反应的受体是不同的。3. 未获得色胺受体异质性的证据。4. 5-羟色胺(5-HT)拮抗剂麦角酰二乙胺和赛庚啶虽然效力很强,但表现出非竞争性拮抗作用,而一系列吩噻嗪类药物和酚妥拉明则对5-HT表现出竞争性拮抗作用。5. 对于吩噻嗪类药物,效力增强的顺序为:异丙嗪<氯丙嗪<三氟拉嗪。

相似文献

5
Antagonism by tetrahydro-beta-carboline of the vasoconstrictor responses to tryptamine in rat tail arteries.
Eur J Pharmacol. 1983 Dec 9;96(1-2):145-9. doi: 10.1016/0014-2999(83)90543-5.

本文引用的文献

1
An action of 5-hydroxytryptamine on adrenaline receptors.5-羟色胺对肾上腺素受体的作用。
Br J Pharmacol Chemother. 1962 Dec;19(3):427-41. doi: 10.1111/j.1476-5381.1962.tb01447.x.
4
The pharmacological differentiation of adrenergic receptors.肾上腺素能受体的药理学分化
Ann N Y Acad Sci. 1967 Feb 10;139(3):553-70. doi: 10.1111/j.1749-6632.1967.tb41229.x.

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