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Therapeutic strategies targeting the ACE2/Ang-(1-7)/Mas axis show compelling preclinical promise for cardiometabolic diseases, though clinical efficacy remains to be established in ongoing trials.
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Highlights emerging therapeutic strategies targeting the ACE2/Ang-(1-7)/Mas axis for cardiometabolic diseases, though clinical efficacy remains to be established.
INTRODUCTION: The renin-angiotensin system (RAS) is a main therapeutic target for cardiovascular diseases. Within the last two decades, novel components of the RAS have been discovered, opening new opportunities to interfere with its activity. Angiotensin(Ang)-(1-7) is synthesized by angiotensin-converting enzyme 2 (ACE2), and interacts with the G-protein-coupled receptor Mas. The axis formed by ACE2/Ang-(1-7)/Mas represents an endogenous counter regulatory pathway within the RAS. AREAS COVERED: In this review, the authors discuss patents and recent initiatives to develop therapeutic strategies based on the ACE2/Ang-(1-7)/Mas axis. EXPERT OPINION: Many publications and patents support a strategy to interfere with the activity of the RAS by stimulating its counter-regulatory axis mainly in two different ways: i) To increase the activity of ACE2, which will impact the system by increasing the inactivation of Ang II and the production of Ang-(1-7); ii) To stimulate Mas, taking advantage of nanostructured formulations of the natural peptide or analogues of Ang-(1-7). Although the preclinical studies are compelling, the possible impact of these novel therapeutic tools for the treatment of cardiometabolic diseases will only be known after completion of the ongoing clinical studies.
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Ferreira et al. (2012) conducted a review in Cardiovascular diseases. ACE2/Ang-(1-7)/Mas axis targeted therapies was evaluated. Therapeutic strategies targeting the ACE2/Ang-(1-7)/Mas axis show compelling preclinical promise for cardiometabolic diseases, though clinical efficacy remains to be established in ongoing trials.
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