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1.
J Spinal Cord Med ; 30(2): 140-6, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-17591226

RESUMO

BACKGROUND/OBJECTIVES: Glutamine plays a key role in immune response. Spinal cord injury (SCI) leads to severe loss of muscle mass and to a high incidence of infections. This study investigated the acute effect of SCI (2 and 5 days) on the plasma glutamine and skeletal muscle concentrations and immune responses in rats. METHODS: A total of 29 adult male Wistar rats were divided as follows: control (C; n = 5), sham-operated (S2; n = 5) and spinal cord-transected (T2; n = 7). They were killed on day 2 after surgery/transection (acute phase). Another set was sham-operated (S5; n = 5), spinal cord-transected (T5; n = 7), and killed at day 5 after surgery/transection (secondary phase). Blood was collected; the white portion of the epitrochlearis and gastrocnemius muscles and the red portion of soleus muscles were dissected to measure the glutamine concentration. Gut-associated lymphocytes and peritoneal macrophages were obtained for immune parameters measurements. RESULTS: Glutamine concentration in the plasma, gastrocnemius, and soleus muscles in rats with SCI were significantly reduced but not in the epitrochlearis muscle in the acute (2 days) and secondary (5 days) phases. Phagocytic response was reduced in the acute phase but increased in the secondary phase in rats with SCI. Superoxide production, on the other hand, was significantly increased at days 2 and 5 after SCI, and CD8+ lymphocytes subset decreased significantly on days 2 and 5. CONCLUSIONS: Our results showed reduction in plasma glutamine and skeletal muscle concentrations after spinal cord transection. They also suggest that SCI and glutamine reduction contribute to an alteration in immune competence.


Assuntos
Infecções Bacterianas/metabolismo , Ácido Glutâmico/sangue , Músculo Esquelético/metabolismo , Atrofia Muscular/metabolismo , Paralisia/complicações , Traumatismos da Medula Espinal/complicações , Animais , Infecções Bacterianas/diagnóstico , Infecções Bacterianas/imunologia , Biomarcadores/análise , Biomarcadores/sangue , Modelos Animais de Doenças , Metabolismo Energético/fisiologia , Ativação Linfocitária/imunologia , Macrófagos/imunologia , Macrófagos/metabolismo , Masculino , Metabolismo/fisiologia , Músculo Esquelético/inervação , Músculo Esquelético/fisiopatologia , Atrofia Muscular/diagnóstico , Atrofia Muscular/imunologia , Peptídeo Hidrolases/metabolismo , Valor Preditivo dos Testes , Ratos , Ratos Wistar , Sepse/diagnóstico , Sepse/imunologia , Sepse/metabolismo , Linfócitos T/imunologia , Linfócitos T/metabolismo
2.
Mol Cell Biochem ; 273(1-2): 145-50, 2005 May.
Artigo em Inglês | MEDLINE | ID: mdl-16013449

RESUMO

The insulin-like effects of peroxovanate (POV) and peroxovanadyl (PSV) on rates of lactate formation and glycogen synthesis were measured in isolated incubated soleus muscle preparations. In another experiment rats were made insulin deficient by streptozotocin injection and treated with POV and PSV (0.25 mM) administered in the drinking water and in the course of 7 days glycemia were determined. Also, signal transduction proteins ERK 1 and ERK 2 involved in the insulin signaling were measured in soleus muscle of diabetic rats treated with POV and PSV. Peroxides of vanadate and vanadyl significantly stimulated glucose utilization in soleus muscle preparations in vitro. The stimulation of glycogen synthesis and lactate formation by POV and PSV was similar to insulin stimuli. Rats treated with POV or PSV presented reduction of glycemia, food and fluid intake with amelioration of the diabetic state during the short period of treatment (7 days). POV and PSV modulated ERK1/2 phosphorilation and the insulin administration in these rats caused an addictive effect on phosphorilation state of these proteins.


Assuntos
Glucose/metabolismo , Hipoglicemiantes/farmacologia , Músculo Esquelético/efeitos dos fármacos , Transdução de Sinais/efeitos dos fármacos , Vanadatos/farmacologia , Compostos de Vanádio/farmacologia , Animais , Diabetes Mellitus Experimental/etiologia , Diabetes Mellitus Experimental/metabolismo , Glicogênio/metabolismo , Hiperglicemia/etiologia , Hiperglicemia/fisiopatologia , Insulina/farmacologia , Ácido Láctico/metabolismo , Masculino , Proteína Quinase 1 Ativada por Mitógeno/metabolismo , Proteína Quinase 3 Ativada por Mitógeno/metabolismo , Músculo Esquelético/citologia , Músculo Esquelético/metabolismo , Fosforilação/efeitos dos fármacos , Ratos , Ratos Wistar , Compostos de Vanádio/química
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