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Klotho, a transmembrane protein that is classically known for its co-receptor activity with fibroblast growth hormone receptors, has recently been characterized as a possible secretagogue for GH

The medication helps by curbing appetite and slowing digestion, which decreases overall calorie intake and supports steady weight loss

doi: 10.1016/j.actbio.2023.10.024 41 LuoYLiCZhangYLiuPChenHZhaoZet al

GLP-1 medications like Ozempic affect multiple body systems through these primary mechanisms: Stimulating insulin secretion: When blood glucose levels rise after meals, Ozempic triggers the pancreas to release insulin in a glucose-dependent manner, helping cells absorb sugar from the bloodstream Decreasing glucagon release: The medication suppresses the hormone glucagon, which normally signals the liver to release stored glucose, thereby preventing unnecessary increases in blood sugar Slowing gastric emptying: By delaying how quickly food leaves the stomach and enters the small intestine, Ozempic prolongs feelings of fullness and reduces post-meal blood sugar spikes this same mechanism (which healthcare providers now recognize) has been linked to severe complications in litigation Affecting brain receptors: The medication acts on GLP-1 receptors in brain regions that control appetite and satiety, contributing to substantial weight loss effects that led to its widespread off-label use The FDA approval in December 2017 marked the beginning of what would become one of the fastest-growing pharmaceutical markets in recent history