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Interestingly, GLP-1 is a hormone naturally produced in the gut after a meal

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At the same time, the chronic inflammation response in the brain that is part of these diseases continues to damage neurons

Triple Receptor Agonism The defining characteristic of retatrutide is its simultaneous activation of three key metabolic hormone receptors: GLP-1 Receptor: Activation increases insulin secretion in a glucose-dependent manner, reduces glucagon secretion, delays gastric emptying, and decreases appetite through central nervous system effects GIP Receptor: Stimulates insulin secretion and enhances the body's response to glucose while potentially improving lipid metabolism Glucagon Receptor: Activation increases energy expenditure and lipid oxidation, which complements the anorectic effects of GLP-1 receptor activation This triple agonism approach is designed to address multiple aspects of metabolic dysfunction simultaneously, potentially offering superior efficacy compared to single or dual receptor agonists[1][2]

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