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Neuroscience ; 131(4): 779-84, 2005.
Artigo em Inglês | MEDLINE | ID: mdl-15749332

RESUMO

Rodents that live in changing environments display different immune responses mediated in part by photoperiod (day length) cues. Siberian hamsters maintained in winter-like (short) photoperiods display smaller physiological and behavioral responses to immune challenges as compared with hamsters housed in summer-like (long) photoperiods. We hypothesized that these different response patterns are attributable to altered cytokine production in the hypothalamus in response to photoperiod changes. Female hamsters were housed in long or short days for 10 weeks to induce photoperiodic alterations, then injected with either LPS (a bacterial endotoxin) or saline. Fever and food intake were assessed 3 h post-injection; hypothalami and blood were collected 3, 6, and 12 h post-injection. LPS induced lower fever and reduction in food intake responses in short-day hamsters as compared with long-day hamsters. Additionally, short-day hamsters reduced IL-1beta and Tnfalpha expression in the hypothalamus 6 h after LPS injection, as measured by quantitative RT-PCR. Plasma estradiol concentrations did not differ between long- and short-day hamsters. These data suggest that differences in cytokine production in the hypothalamus may underlie the photoperiod-induced differences in sickness responses, and that these changes are not mediated by estradiol.


Assuntos
Citocinas/biossíntese , Citocinas/genética , Ingestão de Alimentos/efeitos dos fármacos , Febre/fisiopatologia , Hipotálamo/metabolismo , Lipopolissacarídeos/toxicidade , Fotoperíodo , Animais , Peso Corporal/efeitos dos fármacos , Peso Corporal/fisiologia , Cricetinae , DNA Complementar/biossíntese , DNA Complementar/genética , Ingestão de Alimentos/fisiologia , Estradiol/metabolismo , Feminino , Febre/induzido quimicamente , Interleucina-1/biossíntese , Tamanho do Órgão/efeitos dos fármacos , Tamanho do Órgão/fisiologia , Phodopus , RNA/biossíntese , RNA/isolamento & purificação , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Fator de Necrose Tumoral alfa/biossíntese
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