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血管紧张素II在兔主动脉中组胺介导的肌性效应的证据。

Evidence for the histamine-mediated myotropic effect of angiotensin II in the rabbit aorta.

作者信息

Ercan Z S, Ersoy F F, Bökesoy T A, Türker R K

出版信息

Pharmacology. 1979;18(5):276-9. doi: 10.1159/000137264.

Abstract

Histamine H1-receptor antagonist mepyramine and H2-receptor antagonist metiamide, respectively diminished and potentiated angiotensin II(A II)-induced myotropic responses in the rabbit aortic strips. The responses of the octapeptide were also inhibited in the presence of histidine decarboxylase inhibitor, 2-hydroxy-5-carbomethoxybenzoxyamine and restored when subcontractile quantities of histamine are added to the inhibitor-containing medium. Inhibition of histamine degradation by aminoguanidine potentiates A II's responses. These results are taken as evidences indicating A II-induced histamine synthesis in the test preparation.

摘要

组胺H1受体拮抗剂美吡拉敏和H2受体拮抗剂甲硫米特,分别减弱和增强了血管紧张素II(A II)诱导的兔主动脉条肌性反应。在存在组氨酸脱羧酶抑制剂2-羟基-5-甲氧羰基苄氧胺的情况下,八肽的反应也受到抑制,而当向含抑制剂的培养基中加入亚收缩量的组胺时,反应恢复。氨基胍对组胺降解的抑制增强了A II的反应。这些结果被视为表明在测试制剂中A II诱导组胺合成的证据。

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