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CoPPIX Protects against TNBS Induced Colitis Through HO-1 Induction / 대한해부학회지
Korean Journal of Anatomy ; : 459-466, 2004.
Artículo en Inglés | WPRIM | ID: wpr-650606
ABSTRACT
Crohn`s disease is a severe chronic inflammation that is treated mainly by immunosuppression, which often has serious side effects. There is a need to develop new drugs for treating this disease that have few side effects. Heme oxygenase-1 (HO-1) has immunosuppressive properties, but the mechanism of its anti-inflammatory actions is unclear. We investigated the protective effects of HO-1 on trinitrobenzene sulfonic acid (TNBS)-induced colitis in mice. An HO-1 inducer, cobalt protoporphyrin IX (CoPPIX), dramatically improved the clinical and histopathological symptoms in TNBS-induced colitis. CoPPIX suppressed tumor necrosis factor-alpha and interleukin-1beta expression and down-regulated the nuclear transcription factor kappa B activity caused by TNBS. The vehicle copper protoporphyrin IX (CuPPIX) failed to duplicate the protective effects seen with CoPPIX. Moreover, an inhibitor of HO-1 activity-zinc protoporphyrin IX-reversed the protective effects of CoPPIX on TNBS-induced colitis. In conclusion CoPPIX protects against TNBS-induced colonic damage by inducing HO-1, which might be an important target in the treatment of Crohn`s disease.
Asunto(s)

Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Factores de Transcripción / Terapia de Inmunosupresión / Factor de Necrosis Tumoral alfa / Cobalto / Colitis / Colon / Cobre / Hemo-Oxigenasa 1 / Interleucina-1beta / Inflamación Límite: Animales Idioma: Inglés Revista: Korean Journal of Anatomy Año: 2004 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Factores de Transcripción / Terapia de Inmunosupresión / Factor de Necrosis Tumoral alfa / Cobalto / Colitis / Colon / Cobre / Hemo-Oxigenasa 1 / Interleucina-1beta / Inflamación Límite: Animales Idioma: Inglés Revista: Korean Journal of Anatomy Año: 2004 Tipo del documento: Artículo