Angiotensin-converting enzyme 2 and angiotensin 1-7: novel therapeutic targets

被引:314
作者
Jiang, Fan [1 ]
Yang, Jianmin [1 ]
Zhang, Yongtao [1 ]
Dong, Mei [1 ]
Wang, Shuangxi [1 ]
Zhang, Qunye [1 ]
Liu, Fang Fang [1 ]
Zhang, Kai [1 ]
Zhang, Cheng [1 ]
机构
[1] Shandong Univ, Qilu Hosp, Key Lab Cardiovasc Remodelling & Funct Res, Jinan 250012, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
ATTENUATES DIABETIC-NEPHROPATHY; ROSTRAL VENTROLATERAL MEDULLA; LEFT-VENTRICULAR HYPERTROPHY; ENHANCES PLAQUE STABILITY; SALT-INDUCED HYPERTENSION; RECEPTOR MAS AGONIST; II TYPE-1 RECEPTOR; BLOOD-PRESSURE; HEART-FAILURE; IN-VIVO;
D O I
10.1038/nrcardio.2014.59
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The renin-angiotensin system (RAS) has pivotal roles in the regulation of normal physiology and the pathogenesis of cardiovascular disease. Angiotensin-converting enzyme (ACE) 2, and its product angiotensin 1-7, are thought to have counteracting effects against the adverse actions of other, better known and understood, members of the RAS. The physiological and pathological importance of ACE2 and angiotensin 1-7 in the cardiovascular system are not completely understood, but numerous experimental studies have indicated that these components have protective effects in the heart and blood vessels. Here, we provide an overview on the basic properties of ACE2 and angiotensin 1-7 and a summary of the evidence from experimental and clinical studies of various pathological conditions, such as hypertension, atherosclerosis, myocardial remodelling, heart failure, ischaemic stroke, and diabetes mellitus. ACE2mediated catabolism of angiotensin II is likely to have a major role in cardiovascular protection, whereas the relevant functions and signalling mechanisms of actions induced by angiotensin 1-7 have not been conclusively determined. The ACE2-angiotensin 1-7 pathway, however, might provide a useful therapeutic target for the treatment of cardiovascular disease, especially in patients with overactive RAS.
引用
收藏
页码:413 / 426
页数:14
相关论文
共 218 条
[91]   Tumor necrosis factor-α convertase (ADAM17) mediates regulated ectodomain shedding of the severe-acute respiratory syndrome-coronavirus (SARS-CoV) receptor, angiotensin-converting enzyme-2 (ACE2) [J].
Lambert, DW ;
Yarski, M ;
Warner, FJ ;
Thornhill, P ;
Parkin, ET ;
Smith, AI ;
Hooper, NM ;
Turner, AJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (34) :30113-30119
[92]   Targeting the renin-angiotensin-aldosterone system in heart failure [J].
Lang, Chim C. ;
Struthers, Allan D. .
NATURE REVIEWS CARDIOLOGY, 2013, 10 (03) :125-134
[93]   Involvement of the Gi/o/cGMP/PKG pathway in the AT2-mediated inhibition of outer cortex proximal tubule Na+-ATPase by Ang-(1-7) [J].
Lara, LD ;
Cavalcante, F ;
Axelband, F ;
De Souza, AM ;
Lopes, AG ;
Caruso-Neves, C .
BIOCHEMICAL JOURNAL, 2006, 395 (183-190) :183-190
[94]   Angiotensin (1-7) prevent heart dysfunction and left ventricular remodeling caused by renal dysfunction in 5/6 nephrectomy mice [J].
Li, Yiwen ;
Wu, Jianyong ;
He, Qiang ;
Shou, Zhangfei ;
Zhang, Ping ;
Pen, Wenhan ;
Zhu, Yilin ;
Chen, Jianghua .
HYPERTENSION RESEARCH, 2009, 32 (05) :369-374
[95]   Association of angiotensin-converting enzyme 2 (ACE2) gene polymorphisms with parameters of left ventricular hypertrophy in men -: Results of the MONICA Augsburg echocardiographic substudy [J].
Lieb, W ;
Graf, J ;
Götz, A ;
König, IR ;
Mayer, B ;
Fischer, M ;
Stritzke, J ;
Hengstenberg, C ;
Holmer, SR ;
Döring, A ;
Löwel, H ;
Schunkert, H ;
Erdmann, J .
JOURNAL OF MOLECULAR MEDICINE-JMM, 2006, 84 (01) :88-96
[96]   Potentiation of the hypotensive effect of bradykinin by short-term infusion of angiotensin-(1-7) in normotensive and hypertensive rats [J].
Lima, CV ;
Paula, RD ;
Resende, FL ;
Khosla, MC ;
Santos, RAS .
HYPERTENSION, 1997, 30 (03) :542-548
[97]   Angiotensin-Converting Enzyme (ACE) 2 Overexpression Ameliorates Glomerular Injury in a Rat Model of Diabetic Nephropathy: A Comparison with ACE Inhibition [J].
Liu, Chun Xi ;
Hu, Qin ;
Wang, Yan ;
Zhang, Wei ;
Ma, Zhi Yong ;
Feng, Jin Bo ;
Wang, Rong ;
Wang, Xu Ping ;
Dong, Bo ;
Gao, Fei ;
Zhang, Ming Xiang ;
Zhang, Yun .
MOLECULAR MEDICINE, 2011, 17 (1-2) :59-69
[98]   Angiotensin-(1-7)-induced activation of ERK1/2 is cAMP/protein kinase A-dependent in glomerular mesangial cells [J].
Liu, George C. ;
Oudit, Gavin Y. ;
Fang, Fei ;
Zhou, Joyce ;
Scholey, James W. .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2012, 302 (06) :F784-F790
[99]   Angiotensin-converting enzyme 2 antagonizes angiotensin II-induced pressor response and NADPH oxidase activation in Wistar-Kyoto rats and spontaneously hypertensive rats [J].
Lo, Jennifer ;
Patel, Vaibhav B. ;
Wang, Zuocheng ;
Levasseur, Jody ;
Kaufman, Susan ;
Penninger, Josef M. ;
Oudit, Gavin Y. .
EXPERIMENTAL PHYSIOLOGY, 2013, 98 (01) :109-122
[100]   Angiotensin-(1-7) attenuates the development of heart failure after myocardial infarction in rats [J].
Loot, AE ;
Roks, AJM ;
Henning, RH ;
Tio, RA ;
Suurmeijer, AJH ;
Boomsma, F ;
van Gilst, WH .
CIRCULATION, 2002, 105 (13) :1548-1550