Like other typical GLP-1 agonists, retitrutide is a GGG tri-agonist that selectively activates the glucagon receptor in addition to targeting GLP-1 and GIP receptors. This additional receptor connection increases basal metabolism for more steady fat loss by promoting the synthesis of glucagon, which in turn breaks down glycogen and stored fat. Different from earlier GLP-1 agonists, it offers a complete approach to obesity research through its activities on GIP and GLP-1 receptors, which promote delayed stomach emptying and appetite regulation.
Quantity | 5.0mg, 10.0mg |
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