抗抑郁药对豚鼠回肠组胺H1和毒蕈碱乙酰胆碱受体的影响。

Journal de pharmacologie Pub Date : 1986-04-01
F J Alvarez, E Casas, A Carvajal, A Velasco
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引用次数: 0

摘要

在豚鼠回肠上评价了一些三环和非三环抗抑郁药对拮抗组胺H1和毒蕈碱乙酰胆碱受体的作用。它们像竞争性拮抗剂一样作用于组胺H1受体。其中一些对毒蕈碱类乙酰胆碱受体表现出竞争性拮抗作用,另一些则表现出非竞争性拮抗作用。其中一些药物对组胺H1和/或毒蕈碱乙酰胆碱受体是非常有效的拮抗剂,而其他药物,特别是非三环抗抑郁药,效力很小。所有抗抑郁药的组胺H1活性都高于毒蕈碱乙酰胆碱活性。这些结果不能解释这些药物的治疗效果,但它们可以解释一些副作用和药物相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of antidepressants on histamine H1 and muscarinic acetylcholine receptors in guinea-pig ileum.

The properties of some tricyclic and non-tricyclic antidepressants on antagonist histamine H1 and muscarinic acetylcholine receptors have been evaluated on guinea-pig ileum. They act like competitive antagonists on histamine H1 receptors. Some of them show a competitive antagonism and others a non-competitive antagonism on muscarinic acetylcholine receptors. A few of them are very potent antagonists on histamine H1 and/or muscarinic acetylcholine receptors, while others, especially the non-tricyclic antidepressants, have a small potency. All antidepressants have a higher histamine H1 activity than muscarinic acetylcholine activity. These results cannot explain the therapeutic effect of these drugs, but they can account for some side effects and drug interactions.

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