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α1肾上腺素能受体基因敲除小鼠研究的临床意义

Clinical implications from studies of alpha1 adrenergic receptor knockout mice.

作者信息

Koshimizu Taka-aki, Tanoue Akito, Tsujimoto Gozoh

机构信息

Department of Genomic Drug Discovery Science, Graduate School of Pharmaceutical Sciences, Kyoto University, Yoshida Shimoadachi-cho, Sakyo-ku, Kyoto 606-8501, Japan.

出版信息

Biochem Pharmacol. 2007 Apr 15;73(8):1107-12. doi: 10.1016/j.bcp.2006.11.002. Epub 2006 Nov 7.

Abstract

alpha1-Adrenergic receptors (alpha1-ARs) modulate a large number of physiological functions in cardiovascular and noncardiovascular tissues. Because individual members of the alpha1-AR family (alpha1A-, alpha1B-, and alpha1D-ARs) have overlapping expression profiles in most tissues, elucidation of the precise physiological roles of individual alpha1-AR subtypes remains a challenging task. To alleviate this constraint, a gene targeting approach has been employed to generate mutant mice lacking one or two alpha1-AR genes. Recent studies on these mutant mouse strains are discussed in this article, with an emphasis on the role of alpha1-AR in the central nervous system and lower urinary tracts. These are two major tissues of particular interest for the development of new therapeutic strategies targeted to the alpha1-ARs. By combining gene targeting techniques with pharmacological tools, the specific roles of alpha1-AR subtypes could be delineated.

摘要

α1肾上腺素能受体(α1-ARs)调节心血管组织和非心血管组织中的大量生理功能。由于α1-AR家族的各个成员(α1A-、α1B-和α1D-ARs)在大多数组织中具有重叠的表达谱,阐明各个α1-AR亚型的确切生理作用仍然是一项具有挑战性的任务。为了缓解这一限制,已采用基因靶向方法来生成缺失一个或两个α1-AR基因的突变小鼠。本文讨论了对这些突变小鼠品系的最新研究,重点是α1-AR在中枢神经系统和下尿路中的作用。这是针对α1-ARs开发新治疗策略特别感兴趣的两个主要组织。通过将基因靶向技术与药理学工具相结合,可以描绘出α1-AR亚型的具体作用。

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