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肾脏中的血管紧张素II受体亚型。

Angiotensin II receptor subtypes in the kidney.

作者信息

Edwards R M, Aiyar N

出版信息

J Am Soc Nephrol. 1993 Apr;3(10):1643-52. doi: 10.1681/ASN.V3101643.

Abstract

The kidney is an important target organ for angiotensin II. The diverse biologic effects of angiotensin II in the kidney and periphery suggest that angiotensin II may be interacting with more than one receptor. Recently, the synthesis of highly selective nonpeptide angiotensin II receptor antagonists and the expression cloning of the angiotensin receptor have unequivocally demonstrated the existence of at least two angiotensin II receptor subtypes, designated AT1 and AT2. Autoradiography and ligand binding studies have shown that most tissues, including the kidney, have a mixture of both receptor subtypes. The AT1 receptor is coupled via G proteins to traditional signal transduction mechanisms such as stimulation of phospholipase C, Ca2+ mobilization, and inhibition of adenylate cyclase. The AT2 receptor does not appear to be coupled to G proteins, and the signal transduction pathway(s) associated with this receptor is not known but may involve cGMP. In the kidney, as in the periphery, all of the major physiologic actions of angiotensin II appear to be mediated by activation of the AT1 receptor. In this review, the general characteristics of the AT1 and AT2 receptors and their distribution and function in the kidney will be discussed.

摘要

肾脏是血管紧张素II的重要靶器官。血管紧张素II在肾脏及外周具有多种生物学效应,提示其可能与不止一种受体相互作用。近来,高选择性非肽类血管紧张素II受体拮抗剂的合成以及血管紧张素受体的表达克隆已明确证实至少存在两种血管紧张素II受体亚型,分别命名为AT1和AT2。放射自显影和配体结合研究表明,包括肾脏在内的大多数组织都同时存在这两种受体亚型。AT1受体通过G蛋白与传统信号转导机制偶联,如刺激磷脂酶C、动员Ca2+以及抑制腺苷酸环化酶。AT2受体似乎不与G蛋白偶联,与之相关的信号转导途径尚不清楚,但可能涉及环磷酸鸟苷(cGMP)。在肾脏以及外周,血管紧张素II的所有主要生理作用似乎均由AT1受体的激活介导。在本综述中,将讨论AT1和AT2受体的一般特性及其在肾脏中的分布和功能。

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