Pakala Rajbabu
Cardiovascular Research Institute, Washington Hospital Center, Washington, DC, USA.
Cardiovasc Revasc Med. 2008 Jul-Sep;9(3):166-78. doi: 10.1016/j.carrev.2008.02.001.
Urotensin II (U-II) is a powerful vasoconstrictor peptide with a potency greater than that of endothelin 1. Its plasma level correlates positively with body weight and is raised in diabetes, renal failure, hypertension, and other cardiovascular diseases, including congestive heart failure and carotid atherosclerosis. Experimental and clinical studies have revealed increased expression of U-II and U-II receptor (UT) in animals with experimentally induced myocardial infarction, heart failure, and in patients with hypertension, atherosclerosis, and diabetes, suggesting a potential role for U-II in coronary artery disease. Peptide and nonpeptide UT ligands have been shown to be effective in antagonizing the effects of U-II in the cardiovascular system. This article aims to review recent advances in physiology and pathophysiology of U-II with particular reference to its role in atherosclerotic cardiovascular diseases.
尾加压素II(U-II)是一种强大的血管收缩肽,其效力大于内皮素-1。其血浆水平与体重呈正相关,在糖尿病、肾衰竭、高血压以及其他心血管疾病(包括充血性心力衰竭和颈动脉粥样硬化)中升高。实验和临床研究表明,在实验性诱导心肌梗死、心力衰竭的动物以及高血压、动脉粥样硬化和糖尿病患者中,U-II和U-II受体(UT)的表达增加,提示U-II在冠状动脉疾病中可能发挥作用。肽类和非肽类UT配体已被证明可有效拮抗U-II在心血管系统中的作用。本文旨在综述U-II在生理学和病理生理学方面的最新进展,尤其涉及其在动脉粥样硬化性心血管疾病中的作用。