Isoorientin induces Nrf2 pathway-driven antioxidant response through phosphatidylinositol 3-kinase signaling

被引:0
作者
Ju Hee Lim
Hae-Suk Park
Jung-Kap Choi
Ik-Soo Lee
Hyun Jin Choi
机构
[1] Chonnam National University,College of Pharmacy and Research Institute of Drug Development
来源
Archives of Pharmacal Research | 2007年 / 30卷
关键词
Isoorientin; Oxidative Stress; NF-E2-related factor 2(Nrf2); NAD(P)H:quinone oxi-doreductase 1 (NQO1);
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摘要
Because oxidative stress is involved in the pathogenesis of various chronic diseases and the aging process, antioxidants that can increase the intrinsic antioxidant potency are proposed as desirable therapeutic agents to counteract oxidative stress-related diseases. NF-E2-related factor-2 (Nrf2) is a transcription factor that regulates important antioxidant and phase II detoxification genes, and therefore, the molecule that regulates nuclear translocation of Nrf2 and the induction of antioxidative proteins is thought to be a promising candidate as a cytoprotective agent for oxidative stress. In the present study, we show that isoorientin (Iuteolin 6-C-β-D-glu-coside) obtained from the leaves ofSasa borealis upregulates and activates Nrf2, and has protective ability against oxidative damage caused by reactive oxygen intermediates in HepG2 cells. Isoorientin induces increase in the level of antioxidant enzyme proteins, especially NQO1, and the cytoprotective and antioxidative effects of isoorientin are PI3K/Akt pathway-dependent. Together with direct radical scavenging activity, the novel effect of isoorientin on the regulation of antioxidative gene expression provides attractive strategy to prevent diseases associated with oxidative stress and attenuate the progress of the diseases.
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页码:1590 / 1598
页数:8
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