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[α1-肾上腺素能受体亚型与α1-肾上腺素能受体拮抗剂]

[Alpha1-adrenoceptor subtypes and alpha1-adrenoceptor antagonists].

作者信息

Muramatsu Ikunobu, Suzuki Fumiko, Tanaka Takashi, Yamamoto Hatsumi, Morishima Shigeru

机构信息

Division of Pharmacology, Department of Biochemistry and Bioinformative Sciences, University of Fukui School of Medicine, Japan.

出版信息

Yakugaku Zasshi. 2006 Mar;126 Spec no.:187-98. doi: 10.1248/yakushi.126.187.

Abstract

Alpha(1)-adrenoceptors are widely distributed in the human body and play important physiologic roles. Three alpha(1)-adrenoceptor subtypes (alpha(1A), alpha(1B) and alpha(1D)) have been cloned and show different pharmacologic profiles. In addition, a putative alpha(1)-adrenoceptor (alpha(1L) subtype) has also been proposed. Recently, three drugs (tamsulosin, naftopidil, and silodosin) have been developed in Japan for the treatment of urinary obstruction in patients with benign prostatic hyperplasia. In this review, we describe recent alpha(1)-adrenoceptor subclassifications and the pharmacologic characteristics (subtype selectivity and clinical relevance) of alpha(1)-adrenoceptor antagonists.

摘要

α1肾上腺素能受体广泛分布于人体并发挥重要的生理作用。已克隆出三种α1肾上腺素能受体亚型(α1A、α1B和α1D),且它们表现出不同的药理学特征。此外,还提出了一种假定的α1肾上腺素能受体(α1L亚型)。最近,日本研发出三种药物(坦索罗辛、萘哌地尔和西洛多辛)用于治疗良性前列腺增生患者的尿路梗阻。在本综述中,我们描述了α1肾上腺素能受体的最新分类以及α1肾上腺素能受体拮抗剂的药理学特征(亚型选择性和临床相关性)。

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