抗抑郁药对大鼠离体子宫组胺H2受体的影响。

Journal de pharmacologie Pub Date : 1986-07-01
F J Alvarez, E Casas, A Franganillo, A Velasco
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引用次数: 0

摘要

在大鼠离体子宫中研究了各种抗抑郁药(三环和非三环)以及硫代噻吩对组胺H2受体的拮抗作用。所有研究的药物抑制组胺的作用,作为竞争性拮抗剂。抗组胺H2活性最低的是诺非芬、维洛嗪、曲唑酮和马普替林,而抗组胺H2活性最高的是三氯丙嗪和米安色林,优于西咪替丁。这些结果表明,在大鼠离体子宫中,抗抑郁药与组胺H2受体之间存在类似于抗抑郁药与脑和其他组织中组胺H2受体之间存在的相互作用。
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Effects of antidepressants on histamine H2 receptors in rat isolated uterus.

The antagonist effect of various antidepressants, both tricyclic and non-tricyclic, and of thiothixene on the histamine H2 receptors has been studied in the rat isolated uterus. All the drugs studied inhibit the effect of histamine, acting as competitive antagonists. Trimipramine and mianserin were the antidepressants which showed the highest activity, superior to cimetidine, whereas nomifensine, viloxazine, trazodone and maprotiline were those which showed the lowest antihistamine H2 activity. These results suggest that there is an interaction between antidepressants and histamine H2 receptors in rat isolated uterus similar to the interaction existing between antidepressants and histamine H2 receptors in brain and other tissues.

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