4.7 Article

Growth differentiation factor 15 (GDF15) and semaglutide inhibit food intake and body weight through largely distinct, additive mechanisms

期刊

DIABETES OBESITY & METABOLISM
卷 24, 期 6, 页码 1010-1020

出版社

WILEY
DOI: 10.1111/dom.14663

关键词

animal pharmacology; antiobesity drug; appetite control; GLP-1 analogue; neuropharmacology; weight control

资金

  1. National Institute of Diabetes and Digestive and Kidney Diseases [112812, 119574, 21397]
  2. Pfizer, Inc
  3. Schweizerischer Nationalfonds zur Forderung der Wissenschaftlichen Forschung [P400PB-186728]
  4. Swiss National Science Foundation (SNF) [P400PB_186728] Funding Source: Swiss National Science Foundation (SNF)

向作者/读者索取更多资源

The study aimed to evaluate whether the combination of GDF15 and semaglutide would be a more effective antiobesity treatment and investigate their distinct mechanisms of action. The results showed that combined treatment of GDF15 and semaglutide produced greater weight loss without increasing malaise.
Aims To evaluate whether the potent hypophagic and weight-suppressive effects of growth differentiation factor-15 (GDF15) and semaglutide combined would be a more efficacious antiobesity treatment than either treatment alone by examining whether the neural and behavioural mechanisms contributing to their anorectic effects were common or disparate. Materials/Methods Three mechanisms were investigated to determine how GDF15 and semaglutide induce anorexia: the potentiation of the intake suppression by gastrointestinal satiation signals; the reduction in motivation to feed; and the induction of visceral malaise. We then compared the effects of short-term, combined GDF15 and semaglutide treatment on weight loss to the individual treatments. Rat pharmaco-behavioural experiments assessed whether GDF15 or semaglutide added to the satiating effects of orally gavaged food and exogenous cholecystokinin (CCK). A progressive ratio operant paradigm was used to examine whether GDF15 or semaglutide reduced feeding motivation. Pica behaviour (ie, kaolin intake) and conditioned affective food aversion testing were used to evaluate visceral malaise. Additionally, fibre photometry studies were conducted in agouti-related protein (AgRP)-Cre mice to examine whether GDF15 or semaglutide, alone or in combination with CCK, modulate calcium signalling in hypothalamic AgRP neurons. Results Semaglutide reduced food intake by amplifying the feeding-inhibitory effect of CCK or ingested food, inhibited the activity of AgRP neurons when combined with CCK, reduced feeding motivation and induced malaise. GDF15 induced visceral malaise but, strikingly, did not affect feeding motivation, the satiating effect of ingested food or CCK signal processing. Combined GDF15 and semaglutide treatment produced greater food intake and body weight suppression than did either treatment alone, without enhancing malaise. Conclusions GDF15 and semaglutide reduce food intake and body weight through largely distinct processes that produce greater weight loss and feeding suppression when combined.

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