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Int Immunopharmacol ; 6(11): 1723-8, 2006 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-16979127

RESUMO

Plant flavonoids show anti-inflammatory activity both in vitro and in vivo. Some flavonoids have been reported previously to inhibit nitric oxide (NO) and prostaglandin E2 (PGE2) production by suppressing inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) expression. The present study focuses on the effect of various naturally occurring flavonoids (santin, ermanin, centaureidin and 5,3'-dihydroxy-4'-methoxy-7-methoxycarbonylflavonol) on modulation of lipopolysaccharide (LPS)-induced iNOS and COX-2 expression in RAW 264.7 cells. Western blotting showed that all flavonoids suppressed the induction of both iNOS and COX-2. Ermanin and 5,3'-dihydroxy-4'-methoxy-7-methoxycarbonylflavonol were the most potent inhibitors. This study suggests that inhibition of iNOS and COX-2 expression by flavonoids may be one of the mechanisms responsible for their anti-inflammatory effects, and that they may be potential agents for use in the treatment of inflammatory diseases.


Assuntos
Inibidores de Ciclo-Oxigenase 2/farmacologia , Flavonoides/farmacologia , Óxido Nítrico Sintase Tipo II/antagonistas & inibidores , Tanacetum/química , Animais , Linhagem Celular , Ciclo-Oxigenase 2/metabolismo , Inibidores Enzimáticos/farmacologia , Camundongos , Óxido Nítrico Sintase Tipo II/metabolismo
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