Liraglutide Modulates Appetite and Body Weight Through Glucagon-Like Peptide 1 Receptor-Expressing Glutamatergic Neurons.
Diabetes · 2018
Last updated 2026-05-28A study in mice found that the weight-loss drug liraglutide works by acting on specific brain cells called glutamatergic neurons, not on GABAergic neurons. When liraglutide was given, mice without GLP-1 receptors on glutamatergic neurons did not lose weight or feel sick, and their brain activity changes were blocked. Mice without GLP-1 receptors on GABAergic neurons responded normally to the drug.
AI summary of the abstract below.
| Journal | Diabetes, 2018 |
|---|---|
| Citations | 129 |
| Relative citation ratio | 5.34 |
| NIH percentile | 93 |
| Molecules | liraglutide |
| Conditions studied | Obesity |
Abstract
Glucagon-like peptide 1 receptor (GLP-1R) agonists are U.S. Food and Drug Administration-approved weight loss drugs. Despite their widespread use, the sites of action through which GLP-1R agonists (GLP1RAs) affect appetite and body weight are still not fully understood. We determined whether GLP-1Rs in either GABAergic or glutamatergic neurons are necessary for the short- and long-term effects of the GLP1RA liraglutide on food intake, visceral illness, body weight, and neural network activation. We found that mice lacking GLP-1Rs in -expressing GABAergic neurons responded identically to controls in all parameters measured, whereas deletion of GLP-1Rs in -expressing glutamatergic neurons eliminated liraglutide-induced weight loss and visceral illness and severely attenuated its effects on feeding. Concomitantly, deletion of GLP-1Rs from glutamatergic neurons completely abolished the neural network activation observed after liraglutide administration. We conclude that liraglutide activates a dispersed but discrete neural network to mediate its physiological effects and that these effects require GLP-1R expression on glutamatergic but not GABAergic neurons.
Verbatim abstract via PubMed 29776968 ↗
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