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组胺对兔气管的舒张作用:组胺第三受体亚型可能存在

Relaxant action of histamine on rabbit trachea: possible existence of third histamine receptor subtype.

作者信息

Chand N, Eyre P, DeRoth L

出版信息

Res Commun Chem Pathol Pharmacol. 1979 Feb;23(2):211-21.

PMID:461948
Abstract

The carbachol contracted rabbit trachea relaxes to isoproterenol, PGE1, E2, histamine and bradykinin. Histamine-induced relaxations were resistant to mepyramine (an H1-antagonist), burimamide, cimetidine, metiamide (H2-antagonists), propranolol (a beta-adrenoceptor blocker), indomethacin (a potent inhibitor of prostaglandin synthesis), trasylol (an inhibitor of kallikreins), aminophylline (a purinergic receptor blocker) and dibenzyline (a "D"-tryptamine receptor antagonist). The evidence achieved with these pharmacological agents appears to suggest that the chemical mediator responsible for the relaxant response to histamine is unlikely to be: catecholamines, prostaglandins, 5-HT, adenosine or ATP or kinins. The existence of H2-(iso or H3) histamine receptor subtype in rabbit trachea is postulated.

摘要

卡巴胆碱收缩的兔气管对异丙肾上腺素、前列腺素E1、E2、组胺和缓激肽产生舒张反应。组胺诱导的舒张反应对美吡拉敏(一种H1拮抗剂)、丁咪胺、西咪替丁、甲硫米特(H2拮抗剂)、普萘洛尔(一种β肾上腺素能受体阻滞剂)、吲哚美辛(一种强效前列腺素合成抑制剂)、抑肽酶(一种激肽释放酶抑制剂)、氨茶碱(一种嘌呤能受体阻滞剂)和酚苄明(一种“D”-色胺受体拮抗剂)均有抗性。这些药理学试剂所获得的证据似乎表明,对组胺舒张反应起作用的化学介质不太可能是:儿茶酚胺、前列腺素、5-羟色胺、腺苷或三磷酸腺苷或激肽。推测兔气管中存在H2-(同种或H3)组胺受体亚型。

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