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一种高效且选择性的H3激动剂在体外可使兔大脑中动脉舒张。

A highly potent and selective H3 agonist relaxes rabbit middle cerebral artery, in vitro.

作者信息

Ea-Kim L, Oudart N

机构信息

Laboratoire de Pharmacologie, UFR de Pharmacie, Limoges, France.

出版信息

Eur J Pharmacol. 1988 Jun 10;150(3):393-6. doi: 10.1016/0014-2999(88)90026-x.

Abstract

An H3-agonist, R alpha methylhistamine strongly relaxed isolated and perfused rabbit middle cerebral artery precontracted with K+. This vasodilatation was not antagonized by either mepyramine or cimetidine but was competitively antagonized by an H3-antagonist, a mixture of impromidine and cimetidine. Histamine activated the H3-sites in this artery since its concentration-response curve (obtained with mepyramine and cimetidine) was parallel to that of R alpha methylhistamine. Our data indicate that H3-sites could exist in the rabbit cerebral artery.

摘要

一种H3激动剂,Rα甲基组胺能强烈舒张由钾离子预收缩的离体灌注兔大脑中动脉。这种血管舒张作用既不被美吡拉敏也不被西咪替丁所拮抗,但能被一种H3拮抗剂(英普咪定和西咪替丁的混合物)竞争性拮抗。组胺激活了该动脉中的H3位点,因为其浓度-反应曲线(由美吡拉敏和西咪替丁测得)与Rα甲基组胺的曲线平行。我们的数据表明兔脑动脉中可能存在H3位点。

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