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

被引:31
作者
Ghidewon, M. [1 ,2 ,3 ]
Wald, H. S. [1 ,2 ]
McKnight, A. D. [3 ,4 ]
De Jonghe, B. C. [5 ,6 ]
Breen, D. M. [7 ]
Alhadeff, A. L. [3 ,4 ]
Borner, T. [5 ,6 ]
Grill, H. J. [1 ,2 ]
机构
[1] Univ Penn, Inst Diabet Obes & Metab, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Arts & Sci, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Neurosci, Philadelphia, PA 19104 USA
[4] Monell Chem Senses Ctr, 3500 Market St, Philadelphia, PA 19104 USA
[5] Univ Penn, Sch Nursing, Dept Biobehav Hlth Sci, Philadelphia, PA 19104 USA
[6] Univ Penn, Perelman Sch Med, Dept Psychiat, Philadelphia, PA 19104 USA
[7] Pfizer Global R&D, Internal Med Res Unit, Cambridge, MA USA
基金
瑞士国家科学基金会;
关键词
animal pharmacology; antiobesity drug; appetite control; GLP-1; analogue; neuropharmacology; weight control; NUCLEUS-TRACTUS-SOLITARIUS; RECEPTOR AGONISTS; PEPTIDE-1; NEURONS; NAUSEA; CHOLECYSTOKININ; TOLERABILITY; LIRAGLUTIDE; CONTRIBUTES; APPETITE;
D O I
10.1111/dom.14663
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:1010 / 1020
页数:11
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