
RETATRUTIDE
Unlike the popular well known glucagon-like peptide-1 (GLP-1) receptor agonist medication Semaglutide and unlike Tirzepatide which binds to and activates both GLP-1 and glucose-dependent insulinotropic polypeptide (GIP), Retatrutide has been called a “triple threat”, targeting glucagon (GCG) in addition to GLP-1 and GIP.

Retatrutide, which is an incretin mimetic agent. Incretins decrease appetite and enhance feelings of fullness while slowing gastric emptying (GE). The fewer side effects and high accuracy of incretin mimetic drugs such as liraglutide and semaglutide are opening the door for the development of such drugs. Retatrutide demonstrates similar efficacy to natural glucagon in evoking glucose production within hepatocytes. While in adipocytes, it surpasses native GIP in inducing lipolysis. The data from the trials mentioned in this manuscript indicates that Retatrutide is effective in reducing weight in individuals with non syndromic obesity.
By uniquely targeting three receptors essential to a well functioning metabolism, retatrutide is a triagonist drug that encourages satiation, supports blood sugar regulation, and helps suppress appetite. Pyridoxine may enhance retatrutide’s efficacy while decreasing potential side effects, such as nausea and fatigue. (Evexias)
About Retatrutide/Pyridoxine
Retatrutide, like most weight loss drugs, is part of a class of drugs called glucagon-like peptide-1 (GLP-1) receptor agonists. These drugs imitate the effects of the body’s natural incretin hormone GLP-1 released by the gut following meals that cues the body to release insulin and reduce appetite.
As retatrutide stimulates the release of insulin-boosting GLP-1, it also targets two other hunger-regulating receptors, the glucagon receptor (GCGR) and gastric inhibitory polypeptide receptor (GIPR). Retatrutide’s triple-acting effect helps to combat obesity, type-2 diabetes, and fatty liver disease.