Research

Hormonal

GLP-1 receptor agonists (e.g., Liraglutide) reduce appetite and improve glucose tolerance by stimulating anorexigenic POMC/CART neurons and suppressing orexigenic AgRP/NPY neurons via cAMP and GABA-dependent signaling pathways.

GLP-1 based therapies work by targeting the brain's hunger centers (POMC/CART) to reduce appetite and improve blood sugar control. This suggests that obesity management can involve pharmacological support of natural hormonal signals, rather than relying solely on behavioral changes.

GoodSupportsHIGH confidence
Glucagon-like peptide 1 (GLP-1), a gut-derived hormone capable of decreasing blood sugar levels and improving glucose tolerance by promoting insulin secretion through cyclic adenosine monophosphate (cAMP)-based signaling pathways, can also reduce appetite by directly stimulating proopiomelanocortin (POMC)/cocaine-amphetamine-regulated transcript (CART) (anorexigenic neurons) but suppressing agouti-related protein (AgRP)/neuropeptide Y (NPY) neurons (orexigenic neurons) through γ-aminobutyric acid (GABA)-dependent signaling.
Xue Wen et al. · Signal Transduction and Targeted Therapy · 2022

Why this rating

The paper cites multiple studies (refs 32-38) and notes Liraglutide is already in clinical treatment, indicating strong translational evidence.

Source

Signaling pathways in obesity: mechanisms and therapeutic interventions

Xue Wen et al. · Signal Transduction and Targeted Therapy · 2022

DOI 10.1038/s41392-022-01149-x

narrative_reviewCited 386×
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DOI resolved against Crossref · corpus check 2026-06-10

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