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6-[N,S-二甲基-N'-氰基硫脲基甲基]-6,11-二氢-5H-二苯并[b,e]氮杂卓盐酸盐(Fran 12):一种具有升压特性的组胺和5-羟色胺拮抗剂。

6-[N,S-dimethyl-N'-cyanothioureidomethyl]-6,11-dihydro-5H- dibenz[b,e]azepine hydrochloride (Fran 12): a histamine and 5-hydroxytryptamine antagonist with pressor properties.

作者信息

Law S C, Guyett F J, King R G, Boura A L, Jackson W R, Hodgson W C

机构信息

Department of Pharmacology, Monash University, Clayton, Victoria, Australia.

出版信息

Arch Int Pharmacodyn Ther. 1992 May-Jun;317:67-80.

PMID:1360792
Abstract

We have synthesized and examined some of the pharmacological properties of 6-[N,S-dimethyl-N'-cyanoisothioureidomethyl]-6,11-dihydro-5H- dibenz(b,e)azepine hydrochloride (Fran 12), a derivative of 6-methylaminomethyl-6,11-dihydro-5H- dibenz[b,e,]azepine. In the guinea-pig isolated ileum, Fran 12 (10(-7)-10(-5) M) caused parallel rightward shifts of the concentration-response curves to histamine. A Schild plot gave a pA2 of 7.48, with a slope not significantly different from -1.0. In the rat stomach fundus strip and in endothelium-denuded aortic rings, Fran 12 inhibited contractile responses to 5-hydroxytryptamine in a non-competitive manner. In both chloralose-anaesthetized and pithed rats, it inhibited pressor responses to 5-hydroxytryptamine. It had no effect on depressor responses to 5-hydroxytryptamine in anaesthetized rats. In pithed rats, Fran 12 (0.25-2 mg/kg, i.v.) produced dose-dependent increases in blood pressure. These were not inhibited by i.v. phentolamine, prazosin, yohimbine, propranolol, methysergide, pentolinium or atropine but were inhibited by verapamil. These results indicate that Fran 12 is a histamine and 5-hydroxytryptamine antagonist which also exerts pressor effects via a peripheral action. The pressor action does not appear to be mediated via effects on alpha 1- or alpha 2-adrenoceptors, muscarinic or nicotinic cholinoceptors or 5-hydroxytryptamine receptors, although calcium channel activation may play a role.

摘要

我们合成并研究了6-甲基氨基甲基-6,11-二氢-5H-二苯并[b,e]氮杂䓬的衍生物6-[N,S-二甲基-N'-氰基异硫脲基甲基]-6,11-二氢-5H-二苯并[b,e]氮杂䓬盐酸盐(Fran 12)的一些药理特性。在豚鼠离体回肠中,Fran 12(10⁻⁷ - 10⁻⁵ M)使组胺浓度-反应曲线平行右移。Schild图得出pA2为7.48,斜率与-1.0无显著差异。在大鼠胃底条和去内皮主动脉环中,Fran 12以非竞争性方式抑制对5-羟色胺的收缩反应。在氯醛糖麻醉和脊髓横断的大鼠中,它均抑制对5-羟色胺的升压反应。对麻醉大鼠对5-羟色胺的降压反应无影响。在脊髓横断的大鼠中,Fran 12(0.25 - 2 mg/kg,静脉注射)产生剂量依赖性的血压升高。这些升高不受静脉注射酚妥拉明、哌唑嗪、育亨宾、普萘洛尔、甲基麦角新碱、喷托铵或阿托品的抑制,但受维拉帕米抑制。这些结果表明,Fran 12是一种组胺和5-羟色胺拮抗剂,它还通过外周作用发挥升压效应。升压作用似乎不是通过对α1或α2肾上腺素能受体、毒蕈碱或烟碱胆碱能受体或5-羟色胺受体的作用介导的,尽管钙通道激活可能起作用。

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