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Pharmazie ; 62(12): 933-6, 2007 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-18214346

RESUMO

Panax ginseng is widely used as herbal medicine in East Asia and the pharmacological effects of P. ginseng against certain chronic diseases might be explained by its antioxidative effects. Here, we show that ginsenoside Rd significantly increases both cellular glutathione (GSH) contents and the protein level of gamma-glutamylcysteine ligase (gamma-GCL) heavy chain in H4IIE cells (a rat hepatocyte cell line). Subcellular fractionation and Western blot analysis revealed that ginsenoside Rd increased the nuclear level of p65, but not of Nrf2. Moreover, ginsenoside Rd increased luciferase reporter gene activity in cells transfected with nuclear factor-kappaB (NF-kappaB) binding site-containing -1088 bp gamma-GCL promoter. However, ginsenoside Rd-inducible reporter activity was abolished when cells were transfected with NF-kappaB deletion mutant. These effectsof ginsenoside Rd are suggested to underlie the putative anti-oxidative effect of Panax ginseng.


Assuntos
Antioxidantes/farmacologia , Ginsenosídeos/farmacologia , Glutamato-Cisteína Ligase/biossíntese , Glutationa/metabolismo , NF-kappa B/fisiologia , Animais , Western Blotting , Linhagem Celular , Indução Enzimática , Genes Reporter/efeitos dos fármacos , Glutamato-Cisteína Ligase/genética , Hepatócitos/efeitos dos fármacos , Hepatócitos/metabolismo , Fator 2 Relacionado a NF-E2/biossíntese , Fator 2 Relacionado a NF-E2/genética , Ratos , Fator de Transcrição RelA/biossíntese , Fator de Transcrição RelA/genética
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