Liraglutide Modulates Appetite and Body Weight Through Glucagon-Like Peptide 1 Receptor-Expressing Glutamatergic Neurons.
Jessica M AdamsHongjuan PeiDarleen A SandovalRandy J SeeleyRui B ChangStephen D LiberlesDavid P OlsonPublished in: Diabetes (2018)
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 vGAT-expressing GABAergic neurons responded identically to controls in all parameters measured, whereas deletion of GLP-1Rs in vGlut2-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.
Keyphrases
- body weight
- neural network
- weight loss
- spinal cord
- bariatric surgery
- drug administration
- poor prognosis
- rheumatoid arthritis
- skeletal muscle
- systemic lupus erythematosus
- gastric bypass
- wild type
- spinal cord injury
- binding protein
- ankylosing spondylitis
- body mass index
- risk assessment
- long non coding rna
- endothelial cells
- diabetic rats
- drug induced
- interstitial lung disease
- weight gain