Hepatic structural enhancement and insulin resistance amelioration due to AT1 receptor blockade

• Published in: World journal of hepatology Vol. 9; no. 2; pp. 74 - 79
• Main Author: Vanessa Souza-Mello
• Format: Journal Article
• Language: English
• Published: United States Baishideng Publishing Group Inc 18.01.2017
• Subjects: MAS receptor; Insulin resistance; Non-alcoholic fatty liver disease; Renin-angiotensin system; Angiotensin receptor blockers
• ISSN: 1948-5182; 1948-5182
• DOI: 10.4254/wjh.v9.i2.74

Over the last decade, the role of renin-angiotensin system(RAS) on the development of obesity and its comorbidities has been extensively addressed. Both circulating and local RAS components are up-regulated in obesity and involved in non-alcoholic fatty liver disease onset. Pharmacological manipulations of RAS are viable strategies to tackle metabolic impairments caused by the excessive body fat mass. Renin inhibitors rescue insulin resistance, but do not have marked effects on hepatic steatosis. However, angiotensin-converting enzyme inhibitors and angiotensin receptor blockers(ARB) yield beneficial hepatic remodeling. ARBs elicit body mass loss and normalize insulin levels, tackling insulin resistance. Also, this drug class increases adiponectin levels, besides countering interleukin-6, tumoral necrosis factor-alpha, and transforming growth factor-beta 1. The latter is essential to prevent from liver fibrosis. When conjugated with peroxisome proliferator-activated receptor(PPAR)-alpha activation, ARB fully rescues fatty liver. These effects might be orchestrated by an indirect up-regulation of MAS receptor due to angiotensin Ⅱ receptor type 1(AT1R) blockade. These associations of ARB with PPAR activation and ACE2-angiotensin(ANG)(1-7)-MAS receptor axis deserve a better understanding. This editorial provides a brief overview of the current knowledge regarding AT1 R blockade effects on sensitivity to insulin and hepatic structural alterations as well as the intersections of AT1 R blockade with peroxisome proliferator-activated receptor activation and ACE2-ANG(1-7)- MAS receptor axis.