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阻断尾加压素II系统在系统性高血压中的治疗潜力。

Therapeutic potential of blockade of the urotensin II system in systemic hypertension.

作者信息

Krum Henry, Kemp Will

机构信息

Department of Epidemiology and Preventive Medicine, Monash University/Alfred Hospital, 89 Commercial Road, Melbourne, VIC 3004, Australia.

出版信息

Curr Hypertens Rep. 2007 Mar;9(1):53-8. doi: 10.1007/s11906-007-0010-x.

Abstract

Urotensin II, an 11-amino acid peptide, has been found to be the most potent vasoconstrictor yet described, in certain vascular beds. Discovery of its endogenous receptor (UII-R) has ignited considerable interest in this system's role in disease states associated with increased vascular tone (eg, systemic hypertension). Urotensin II was shown to have direct effects on the heart in addition to effects on vascular tone. In human systemic hypertension, increased plasma levels of urotensin II were noted, with a weak but significant correlation to absolute blood pressure levels. Furthermore, hypertensive patients demonstrate net vasoconstrictor responsiveness in skin microcirculation compared to normal controls. Highly selective UII-R antagonists have been developed based on the known structure of UII-R. Early preclinical and clinical studies report potential beneficial effects in renal disease, heart failure, and diabetes, although effects on blood pressure have been equivocal.

摘要

尾加压素II是一种由11个氨基酸组成的肽,在某些血管床中,它被发现是迄今所描述的最强效的血管收缩剂。其内源性受体(UII-R)的发现引发了人们对该系统在与血管张力增加相关的疾病状态(如系统性高血压)中所起作用的浓厚兴趣。研究表明,尾加压素II除了对血管张力有影响外,还对心脏有直接作用。在人类系统性高血压中,发现尾加压素II的血浆水平升高,且与绝对血压水平存在微弱但显著的相关性。此外,与正常对照组相比,高血压患者的皮肤微循环表现出净血管收缩反应性。基于UII-R的已知结构,已经开发出了高选择性的UII-R拮抗剂。早期的临床前和临床研究报告了其在肾脏疾病、心力衰竭和糖尿病方面的潜在有益作用,尽管对血压的影响尚不明确。

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