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Growth differentiation factor 15 (GDF15) and semaglutide inhibit food intake and body weight through largely distinct, additive mechanisms.
Ghidewon, M; Wald, H S; McKnight, A D; De Jonghe, B C; Breen, D M; Alhadeff, A L; Borner, T; Grill, H J.
Afiliación
  • Ghidewon M; Institute of Diabetes, Obesity and Metabolism and School of Arts and Sciences, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Wald HS; Department of Neuroscience, University of Pennsylvania, Philadelphia, Pennsylvania.
  • McKnight AD; Institute of Diabetes, Obesity and Metabolism and School of Arts and Sciences, University of Pennsylvania, Philadelphia, Pennsylvania.
  • De Jonghe BC; Department of Neuroscience, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Breen DM; Monell Chemical Senses Center, Philadelphia, Pennsylvania.
  • Alhadeff AL; Department of Biobehavioral Health Sciences, School of Nursing, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Borner T; Department of Psychiatry, University of Pennsylvania, Perelman School of Medicine, Philadelphia, Pennsylvania.
  • Grill HJ; Internal Medicine Research Unit, Pfizer Global R&D, Cambridge, Massachusetts.
Diabetes Obes Metab ; 24(6): 1010-1020, 2022 06.
Article en En | MEDLINE | ID: mdl-35129264
ABSTRACT

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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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Pérdida de Peso / Ingestión de Alimentos / Péptidos Similares al Glucagón / Factor 15 de Diferenciación de Crecimiento Límite: Animals Idioma: En Revista: Diabetes Obes Metab Asunto de la revista: ENDOCRINOLOGIA / METABOLISMO Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Pérdida de Peso / Ingestión de Alimentos / Péptidos Similares al Glucagón / Factor 15 de Diferenciación de Crecimiento Límite: Animals Idioma: En Revista: Diabetes Obes Metab Asunto de la revista: ENDOCRINOLOGIA / METABOLISMO Año: 2022 Tipo del documento: Article