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Rev. bras. pesqui. méd. biol ; Braz. j. med. biol. res;50(2): e5801, 2017. graf
Artigo em Inglês | LILACS | ID: biblio-839250

RESUMO

We determined the effect of N-acetylcysteine (NAC) on the expression of the phosphorylated p38 (p-p38) protein and superoxide anion generation (SAG), two important players in the processing of neuropathic pain, in the lumbosacral spinal cord of rats with chronic constriction injury (CCI)-induced neuropathic pain. The sciatic functional index (SFI) was also measured to assess the functional recovery post-nerve lesion. Thirty-six male Wistar rats were divided equally into the following groups: Naive (rats did not undergo surgical manipulation); Sham (rats in which all surgical procedures involved in CCI were used except the ligature), and CCI (rats in which four ligatures were tied loosely around the right common sciatic nerve), which received 2, 4, or 8 intraperitoneal injections of NAC (150 mg·kg-1·day-1) or saline beginning 4 h after CCI. Rats were sacrificed 1, 3, and 7 days after CCI. The SFI was measured on these days and the lumbosacral spinal cord was used for analysis of p-p38 expression and SAG. CCI induced a decrease in SFI as well as an increase in p-p38 expression and SAG in the spinal cord. The SFI showed a partial recovery at day 7 in saline-treated CCI rats, but recovery was improved in NAC-treated CCI rats. NAC induced a downregulation in p-p38 expression at all time-points evaluated, but did not reverse the increased SAG induced by CCI. Since p-p38 is a mediator in neuropathic pain and/or nerve regeneration, modulation of this protein may play a role in NAC-induced effects in CCI rats.


Assuntos
Animais , Masculino , Ratos , Acetilcisteína/uso terapêutico , Neuralgia/tratamento farmacológico , Proteínas Quinases p38 Ativadas por Mitógeno/efeitos dos fármacos , Medula Espinal/efeitos dos fármacos , Superóxidos/metabolismo , Western Blotting , Constrição Patológica , Modelos Animais de Doenças , Regulação para Baixo/efeitos dos fármacos , Neuralgia/etiologia , Proteínas Quinases p38 Ativadas por Mitógeno/metabolismo , Limiar da Dor , Fosforilação/efeitos dos fármacos , Ratos Wistar , Medula Espinal/metabolismo
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