Effects of antidepressants on histamine H1 and muscarinic acetylcholine receptors in guinea-pig ileum.

Journal de pharmacologie Pub Date : 1986-04-01
F J Alvarez, E Casas, A Carvajal, A Velasco
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Abstract

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.

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。
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。
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