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Overfeeding-induced weight gain suppresses plasma ghrelin levels in rats.
Williams, D L; Grill, H J; Cummings, D E; Kaplan, J M.
Afiliação
  • Williams DL; Department of Psychology, University of Pennsylvania, Philadelphia, USA. dianalw@u.washington.edu
J Endocrinol Invest ; 29(10): 863-8, 2006 Nov.
Article em En | MEDLINE | ID: mdl-17185893
ABSTRACT
The elevation of plasma ghrelin associated with weight loss has been taken as evidence of a role for ghrelin in the adaptive response to body weight change. However, there has been no clear experimental evidence that circulating ghrelin is suppressed by weight gain. We investigate this issue using a model of involuntary (intra-gastric gavage) overfeeding-induced obesity. Rats were first maintained at normal body weight with 4 daily tube-feedings of liquid diet (2.11 kcal/ml), each delivered at a volume of 9 ml. Gavage volume was then increased to 13 ml/feeding for 2 weeks, during which rats gained 25% of their initial body weight. Fasting plasma ghrelin levels and the response to 9- and 13-ml intra-gastric load sizes were measured during the weight-stable and overfed conditions. We found that 1) weight gain decreased circulating ghrelin levels; 2) this response could not be attributed to additional food in the gastrointestinal tract; 3) the ghrelin response to nutrient loads was diminished in the obese vs normal-weight conditions. Having discounted diet composition and differences in gastric contents at the time of blood sampling, the decrease in ghrelin levels with overfeeding can be unambiguously attributed to physiological correlates of weight gain.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aumento de Peso / Hiperfagia / Hormônios Peptídicos Tipo de estudo: Etiology_studies Limite: Animals Idioma: En Revista: J Endocrinol Invest Ano de publicação: 2006 Tipo de documento: Article País de afiliação: Estados Unidos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aumento de Peso / Hiperfagia / Hormônios Peptídicos Tipo de estudo: Etiology_studies Limite: Animals Idioma: En Revista: J Endocrinol Invest Ano de publicação: 2006 Tipo de documento: Article País de afiliação: Estados Unidos