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Physiol Behav ; 133: 141-51, 2014 Jun 22.
Artigo em Inglês | MEDLINE | ID: mdl-24866911

RESUMO

Anorexia and anxiety cause significant mortality and disability with female biases and frequent comorbidity after puberty, but the scarcity of suitable animal models impedes understanding of their biological underpinnings. It is reported here that in adult or weanling Syrian hamsters, relative to social housing (SH), social separation (SS) induced anorexia characterized as hypophagia, weight loss, reduced adiposity, and hypermetabolism. Following anorexia, SS increased reluctance to feed, and thigmotaxis, in anxiogenic environments. Importantly, anorexia and anxiety were induced post-puberty with female biases. SS also reduced hypothalamic corticotrophin-releasing factor mRNA and serum corticosteroid levels assessed by RT-PCR and RIA, respectively. Consistent with the view that sex differences in adrenal suppression contributed to female biases in anorexia and anxiety by disinhibiting neuroimmune activity, SS elevated hypothalamic interleukin-6 and toll-like receptor 4 mRNA levels. Although corticosteroids were highest during SH, they were within the physiological range and associated with juvenile-like growth of white adipose, bone, and skeletal muscle. These results suggest that hamsters exhibit plasticity in bioenergetic and emotional phenotypes across puberty without an increase in stress responsiveness. Thus, social separation of hamsters provides a model of sex differences in anorexia and anxiety during adulthood and their pathogeneses during adolescence.


Assuntos
Anorexia/etiologia , Ansiedade/etiologia , Viés , Corticosteroides/sangue , Animais , Peso Corporal/fisiologia , Hormônio Liberador da Corticotropina/genética , Hormônio Liberador da Corticotropina/metabolismo , Cricetinae , Modelos Animais de Doenças , Ingestão de Alimentos , Metabolismo Energético , Comportamento Exploratório , Feminino , Hipotálamo/metabolismo , Interleucina-6/genética , Interleucina-6/metabolismo , Masculino , Mesocricetus , Fatores Sexuais , Isolamento Social/psicologia , Receptor 4 Toll-Like/genética , Receptor 4 Toll-Like/metabolismo
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