Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros

Base de dados
Ano de publicação
Tipo de documento
Intervalo de ano de publicação
1.
Brain Behav Immun ; 36: 90-100, 2014 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-24145051

RESUMO

Toll-like receptors (TLR) are innate immune receptors typically activated by microbial-associated molecular patterns (MAMPs) during infection or damage-associated molecular patterns (DAMPs) as a result of tissue injury. Recent findings suggest that TLR2 and TLR4 signaling play important roles in developmental and adult neuroplasticity, and in learning and memory. In addition, activation of TLR2 and TLR4 worsens ischemic injury to the heart and brain in animal models of myocardial infarction and stroke. TLR activation is also implicated in thermoregulation and fever in response to infection. However, it is not known whether TLRs participate in the regulation of the sympathetic and/or parasympathetic components of the autonomic nervous system (ANS). Here we provide evidence that TLR2 and TLR4 influence autonomic regulation of heart rate (HR) body temperature and energy metabolism in mice. We show that mice lacking TLR2 or TLR4 exhibit reduced basal HR, which results from an increase of parasympathetic tone. In addition, thermoregulatory responses to stress are altered in TLR2-/- and TLR4-/- mice, and brown fat-dependent thermoregulation is altered in TLR4-/- mice. Moreover, TLR2-/- and TLR4-/- mice consume less food and exhibit a greater mass compared to wild type mice. Collectively, our findings suggest important roles for TLR2 and TLR4 in the ANS regulation of cardiovascular function, thermoregulation, and energy metabolism.


Assuntos
Sistema Nervoso Autônomo/fisiologia , Receptor 2 Toll-Like/genética , Receptor 4 Toll-Like/genética , Animais , Temperatura Corporal , Regulação da Temperatura Corporal/fisiologia , Metabolismo Energético/fisiologia , Frequência Cardíaca/fisiologia , Masculino , Camundongos , Camundongos Knockout , Restrição Física , Estresse Psicológico/metabolismo
2.
Age (Dordr) ; 34(6): 1453-8, 2012 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-22037865

RESUMO

Calorie restriction (CR) is a reliable anti-aging intervention that attenuates the onset of a number of age-related diseases, reduces oxidative damage, and maintains function during aging. In the current study, we assessed the effects of CR and other feeding regimens on wound healing in 7-month-old Fischer-344 rats from a larger cohort of rats that had been fed either ad libitum (AL) or 40% calorie restricted based on AL consumption. Rats were assigned to one of three diet groups that received three skin punch wounds along the dorsal interscapular region (12-mm diameter near the front limbs) of the back as follows: (1) CR (n = 8) were wounded and maintained on CR until they healed, (2) AL (n = 5) were wounded and maintained on AL until wound closure was completed, and (3) CR rats were refed (RF, n = 9) AL for 48 h prior to wounding and maintained on AL until they healed. We observed that young rats on CR healed more slowly while CR rats refed for 48 h prior to wounding healed as fast as AL fed rats, similar to a study reported in aged CR and RF mice (Reed et al. 1996). Our data suggest that CR subjects, regardless of age, fail to heal well and that provision of increased nutrition to CR subjects prior to wounding enhances the healing process.


Assuntos
Ingestão de Energia/fisiologia , Privação de Alimentos/fisiologia , Pele/lesões , Cicatrização/fisiologia , Animais , Ingestão de Energia/genética , Metabolismo Energético/genética , Metabolismo Energético/fisiologia , Matriz Extracelular/genética , Matriz Extracelular/fisiologia , Canais Iônicos/genética , Canais Iônicos/fisiologia , Masculino , Proteínas Mitocondriais/genética , Proteínas Mitocondriais/fisiologia , Estresse Oxidativo/genética , Estresse Oxidativo/fisiologia , Coativador 1-alfa do Receptor gama Ativado por Proliferador de Peroxissomo , Proteínas de Ligação a RNA/genética , Proteínas de Ligação a RNA/fisiologia , Ratos , Ratos Endogâmicos F344 , Sirtuína 1/genética , Sirtuína 1/fisiologia , Transativadores/genética , Fatores de Transcrição/genética , Fatores de Transcrição/fisiologia , Proteína Desacopladora 1 , Cicatrização/genética
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA