Nrf2 is involved in the effect of tanshinone IIA on intracellular redox status in human aortic smooth muscle cells
- 作者：Hong-Sheng Zhang ; Sheng-Qi Wang
- 关键词：Tanshinone IIA ; Nrf2 ; Oxidative stress ; Smooth muscle cells
- 刊名：Biochemical Pharmacology
- 出版年：2007
- 期刊代码：2_00062952
- 类别：pha
- 出版时间：1 May 2007
- 卷：73
- 期：9
- 页码：1358-1366
- 文件大小：727 K
摘要
Tanshinone IIA is the major antioxidant component in the traditional Chinese medicine Salvia miltiorrhiza. Transcription factor nuclear-factor-E2-related factor (Nrf2) regulates a battery of antioxidant response element (ARE)-regulated genes. The aim of this study was to determine the effect of tanshinone IIA on Nrf2 activation and intracellular redox status in human aortic smooth muscle cells. Tanshinone IIA potentiated tumor necrosis factor α (TNF-α)-mediated nuclear accumulation of Nrf2 and expression of ARE-related genes, while it reversed TNF-α-induced down-regulation of intracellular glutathione (GSH), NADPH and glucose 6-phosphate dehydrogenase (G6PDH) levels. Specific silence of Nrf2 by siRNA down-regulated tanshinone IIA-induced Nrf2 activation and increased of intracellular GSH, NADPH and G6PDH levels. Tanshinone IIA-induced Nrf2 activation was association with activation of ERK and PKB, which was prevented by treatment with PD098059 or wortmannin. Tanshinone IIA attenuated TNF-α, angiotensin II, H2O2-mediated reactive oxygen species (ROS) production. These results demonstrated that tanshinone IIA-induced Nrf2 activation is the major regulatory pathway of cytoprotective gene expression against oxidative stress via ERK and PKB signaling pathways.