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Curr Pharm Biotechnol ; 14(11): 975-84, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-24372242

RESUMO

Acetaminophen is a common analgesic and antipyretic compound which, when administered in high doses, has been associated with significant morbidity and mortality, secondary to hepatic toxicity. Although this may be due to a direct interaction of reactive acetaminophen metabolites with hepatocyte proteins, recent studies have suggested that reactive species produced by neutrophils also contribute to the pathophysiological process. Researches on the chemical composition of B. trimera show that this plant has bioactive compounds such as flavonoids, related to the organism's protection against free radicals. Therefore, in the present study, using Fischer rats, the effect of B. trimera on the antioxidant defense system, the production of nitric oxide (NO) and on the expression of nitric oxide synthase (iNOS), superoxide dismutase (SOD), catalase (CAT) and of the subunits of the NADPH oxidase in neutrophils was evaluated in a model of phagocytosis induced by zimosan (ZC3b) and in a model of inflammation induced by acetaminophen. The results show that the treatment with B. trimera improves the defense system of antioxidant and restores the balance ROS / NO that is altered in the inflammatory process induced by APAP. In conclusion, B. trimera extracts exert antioxidant properties by scavenging ROS and decrease the expression of genes responsible by reactive species production in neutrophils.


Assuntos
Baccharis/química , Inflamação/tratamento farmacológico , Inflamação/imunologia , NADPH Oxidases/imunologia , Óxido Nítrico Sintase Tipo II/imunologia , Extratos Vegetais/uso terapêutico , Espécies Reativas de Oxigênio/imunologia , Acetaminofen , Animais , Células Cultivadas , Ativação Enzimática/efeitos dos fármacos , Ativação Enzimática/imunologia , Imunidade Inata/efeitos dos fármacos , Imunidade Inata/imunologia , Inflamação/induzido quimicamente , Masculino , Ativação de Neutrófilo/efeitos dos fármacos , Ativação de Neutrófilo/imunologia , Óxido Nítrico Sintase Tipo II/antagonistas & inibidores , Ratos , Ratos Endogâmicos F344 , Resultado do Tratamento
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