The renin-angiotensin-aldosterone system and its therapeutic targets

被引:121
|
作者
Colafella, Katrina M. Mirabito [1 ,2 ]
Bovee, Dominique M. [3 ]
Danser, A. H. Jan [3 ]
机构
[1] Monash Univ, Biomed Discover Inst, Cardiovasc Dis Program, Melbourne, Vic, Australia
[2] Monash Univ, Dept Physiol, Melbourne, Vic, Australia
[3] Erasmus MC, Dept Internal Med, Div Pharmacol & Vasc Med, Univ Med Ctr, Rotterdam, Netherlands
基金
英国医学研究理事会;
关键词
Mineralocorticoid receptor antagonist; Angiotensin-converting enzyme inhibitor; AT(1) receptor blocker; Renin inhibitor; Angiotensinogen siRNA; AT(2) receptor agonist; Neprilysin inhibitor; Mas receptor agonist; ACE2; CONVERTING ENZYME 2; MINERALOCORTICOID RECEPTOR ANTAGONISM; LEFT-VENTRICULAR DYSFUNCTION; REDUCES BLOOD-PRESSURE; II TYPE-2 RECEPTOR; HEART-FAILURE; VASCULAR PATHOLOGY; LIVER ANGIOTENSINOGEN; NEPRILYSIN INHIBITION; DIABETIC-RETINOPATHY;
D O I
10.1016/j.exer.2019.05.020
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
The renin-angiotensin-aldosterone system (RAAS) plays a pivotal role in the regulation of blood pressure and body fluid homeostasis and is a mainstay for the treatment of cardiovascular and renal diseases. Angiotensin II and aldosterone are the two most powerful biologically active products of the RAAS, inducing all of the classical actions of the RAAS including vasoconstriction, sodium retention, tissue remodeling and pro-inflammatory and pro-fibrotic effects. In recent years, new components of the RAAS have been discovered beyond the classical pathway that have led to the identification of depressor or so-called protective RAAS pathways and the development of novel therapies targeting this system. Moreover, dual inhibitors which block the RAAS and other systems involved in the regulation of blood pressure or targeting upstream of angiotensin II by selectively deleting liver-derived angiotensinogen, the precursor to all angiotensins, may provide superior treatment for cardiovascular and renal diseases and revolutionize RAAS-targeting therapy.
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页数:7
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