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通过药理学拮抗作用对兔逼尿肌对组胺的反应进行表征。

Characterization of the rabbit detrusor response to histamine through pharmacologic antagonism.

作者信息

Fredericks C M

出版信息

Pharmacology. 1975;13(1):5-11. doi: 10.1159/000136879.

Abstract

The various effects of histamine on smooth muscles and other tissues are thought to be mediated by two pharmacologically distinct receptors, H1 and H2 types. These receptors are defined in terms of thier susceptibility to blockade by pyrilamine (type H1) or burimamide (type H2). In this study selective antagonism of the spasmodic effects of histamine on isolated strips of rabbit detrusor has shown that the response is mediated by H1 receptors, with no evidence of H2 activity. The p-A2 of the pyrilaminehistamine antagonism is 9.3. The histamine response is susceptible to muscarinic blockade (atropine and propantheline) but not to nicotinic blockade (hexamethonium). Adrenergic blocking agents propranolol (10 minus 4 M) and phenoxybenzamine (10 minus 8 M) do antagonize the contractile response, but this does not appear to be indicative of adrenergic mediation.

摘要

组胺对平滑肌和其他组织的各种作用被认为是由两种药理学特性不同的受体介导的,即H1型和H2型。这些受体是根据它们对吡苄明(H1型)或布立马胺(H2型)阻断作用的敏感性来定义的。在本研究中,对组胺作用于兔逼尿肌离体条带的痉挛效应进行的选择性拮抗作用表明,该反应是由H1受体介导的,没有H2活性的证据。吡苄明 - 组胺拮抗作用的pA2为9.3。组胺反应易受毒蕈碱阻断(阿托品和丙胺太林)影响,但不受烟碱阻断(六甲铵)影响。肾上腺素能阻断剂普萘洛尔(10⁻⁴M)和酚苄明(10⁻⁸M)确实能拮抗收缩反应,但这似乎并不表明是由肾上腺素能介导的。

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