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NMEG-CGRP is a peptoid-modified analog of alpha-calcitonin gene-related peptide (α-CGRP) developed by researchers at the University of South Carolina. It consists of human α-CGRP with two N-methoxyethylglycine (NMEG) peptoid units attached to the N-terminus. This modification is designed to enhance the peptide's bioavailability and stability by protecting it from enzymatic degradation, specifically by insulin-degrading enzyme (IDE). In preclinical studies involving a transverse aortic constriction (TAC) mouse model of pressure-overload heart failure, NMEG-CGRP demonstrated significant cardioprotective effects, including improved fractional shortening and reduced cardiac cell size, fibrosis, and apoptosis. It acts as a bioactive CGRP receptor agonist and vasodilator, positioning it as a potential therapeutic agent for heart failure.
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