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Simultaneous engagement of GLP-1, GIP, and glucagon receptors Modulation of integrated metabolic signaling networks Effects on energy homeostasis pathways Interaction with endocrine feedback systems Participation in glucose and lipid metabolism models Influence on appetite-related neuroendocrine signaling Why it matters: Multi-receptor activity may help explain why Retatrutide is studied differently from single-pathway GLP-1 compounds

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