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Urotensin II and cardiovascular diseases
被引:37
|作者:
Thanassoulis, G
[1
]
Huyhn, T
[1
]
Giaid, A
[1
]
机构:
[1] McGill Univ, Montreal Gen Hosp, Dept Med, Montreal, PQ H3G 1A4, Canada
来源:
关键词:
vascular physiology;
atherosclerosis;
coronary artery disease;
heart failure;
metabolic syndrome;
D O I:
10.1016/j.peptides.2004.05.027
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Urotensin II (UII) has been found to be a potent vasoactive peptide in humans and in a number of relevant animal models of cardiovascular disease such as the mouse, rat and other non-human primates. This peptide with structural homology to somatostatin was first isolated from the urophysis of fish and was recently found to bind to an orphan receptor in mouse and human. Initially found to have potent vasoconstrictive activities in a variety of vessels from diverse species, it has also been shown to exert vasodilatation in certain vessels in the rat and human by various endothelium-dependent mechanisms. The various vasoactive properties of UII suggest that the peptide may have a physiological role in maintaining vascular tone and therefore may have a role in the pathophysiology of a number of human diseases such as heart failure. Moreover, UII has also been implicated as a mitogen of vascular smooth muscle cells suggesting a deleterious role in atherosclerosis and coronary artery disease. In addition, there is evidence to demonstrate that UII has multiple metabolic effects on cholesterol metabolism, glycemic control and hypertension and therefore may be implicated in the development of insulin resistance and the metabolic syndrome. (C) 2004 Elsevier Inc. All rights reserved.
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页码:1789 / 1794
页数:6
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