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While not shown, this is most likely mediated by activation of GLP-1Rs in upstream CCK-expressing NTS neurons by exendin-4 since NE-expressing NTS neurons do not appreciably express GLP-1Rs [66]
How It Works Activates both GLP-1 and GIP receptors for a broader metabolic impact Reduces appetite and increases satiety through two hormonal pathways Enhances insulin sensitivity more aggressively than GLP-1 alone Supports reduction of visceral fat the deep abdominal fat most strongly associated with metabolic disease Improves blood sugar regulation through a dual insulin-stimulating mechanism Clinical Results In the SURMOUNT-1 trial, Tirzepatide produced average weight loss of up to 20% of body weight outperforming Semaglutide in head-to-head comparisons
The consumer is not leaving, they are changing
The mechanism is elegant: mimic a gut hormone that tells your brain you are full, and appetite drops dramatically
Muhammed A, Thomas C, Kalaiselvan V, Undela K
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