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Inhibitory Effect of Esculetin on the Inducuble Nitric Oxide Synthase Expression in TNF-stimulated 3T3-L1 Adipocytes
The Korean Journal of Physiology and Pharmacology ; : 283-287, 2003.
Artículo en Inglés | WPRIM | ID: wpr-727404
ABSTRACT
While nitric oxide (NO) produced by inducible nitric oxide synthase (iNOS) is beneficial for host survival, it is also detrimental to the host. Thus, regulation of iNOS gene expression may be an effective therapeutic strategy for the prevention of unwanted reactions at various pathologic conditions. During the screening process for the possible iNOS regulators, we observed that esculetin is a potent inhibitor of cytokine-induced iNOS expression. The treatment of 3T3-L1 adipocytes with the tumor necrosis factor-alpha (TNF) induced iNOS expression, leading to enhanced NO production. TNF-induced NO production was inhibited by esculetin in a dose-dependent manner. Esculetin inhibited the TNF-induced NO production at the transcriptional level through suppression of iNOS mRNA and subsequent iNOS protein expression. These results suggest esculetin, a component of natural products, as a naturally occurring, nontoxic means to attenuate iNOS expression and NO-mediated cytotoxicity.
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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Productos Biológicos / ARN Mensajero / Expresión Génica / Tamizaje Masivo / Factor de Necrosis Tumoral alfa / Adipocitos / Óxido Nítrico Sintasa / Óxido Nítrico Sintasa de Tipo II / Óxido Nítrico Tipo de estudio: Estudio pronóstico / Estudio de tamizaje Idioma: Inglés Revista: The Korean Journal of Physiology and Pharmacology Año: 2003 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Productos Biológicos / ARN Mensajero / Expresión Génica / Tamizaje Masivo / Factor de Necrosis Tumoral alfa / Adipocitos / Óxido Nítrico Sintasa / Óxido Nítrico Sintasa de Tipo II / Óxido Nítrico Tipo de estudio: Estudio pronóstico / Estudio de tamizaje Idioma: Inglés Revista: The Korean Journal of Physiology and Pharmacology Año: 2003 Tipo del documento: Artículo