Kang Eun Sil, Woo Im Sun, Kim Hyo Jung, Eun So Young, Paek Kyung Shin, Kim Hye Jung, Chang Ki Churl, Lee Jae Heun, Lee Hoon Taek, Kim Jin-Hoi, Nishinaka Toru, Yabe-Nishimura Chihiro, Seo Han Geuk
Department of Pharmacology, Gyeongsang Institute of Health Science, College of Medicine, Gyeongsang National University, 92 Chilam-Dong, Jinju 660-751, Korea.
Free Radic Biol Med. 2007 Aug 15;43(4):535-45. doi: 10.1016/j.freeradbiomed.2007.05.006. Epub 2007 May 16.
Up-regulation of aldose reductase (AR) by reactive oxygen species (ROS) and aldehyde derivatives has been observed in vascular smooth muscle cells. However, the pathophysiological consequences of the induction of AR in vascular tissues are not fully elucidated. Herein we report that an herb-derived polyphenolic compound, curcumin, elicited a dose- and time-dependent increase in AR expression. Inhibition of phosphatidylinositol 3-kinase (PI3K) and p38 mitogen-activated protein kinase (MAPK) significantly suppressed the curcumin-augmented mRNA levels and promoter activity of the AR gene. Luciferase reporter assays indicated that an osmotic response element in the promoter was essential for the responsiveness to curcumin. Curcumin accelerated the nuclear translocation of nuclear factor-erythroid 2-related factor 2 (Nrf2), and overexpression of Nrf2, but not the dominant negative Nrf2, enhanced the promoter activity of the AR gene. Cells preincubated with curcumin demonstrated resistance to ROS-induced apoptotic death. These effects were significantly attenuated in the presence of AR inhibitors or small interfering RNAs, indicating a protective role for AR against ROS-induced cell damage. Taken together, the activation of PI3K and p38 MAPK by curcumin augmented the expression of the AR gene via Nrf2, and increased AR activity may be an important cellular response against oxidative stress.
活性氧(ROS)和醛衍生物可使血管平滑肌细胞中的醛糖还原酶(AR)上调。然而,AR在血管组织中诱导产生的病理生理后果尚未完全阐明。在此我们报告,一种源自草药的多酚化合物姜黄素可引起AR表达呈剂量和时间依赖性增加。抑制磷脂酰肌醇3激酶(PI3K)和p38丝裂原活化蛋白激酶(MAPK)可显著抑制姜黄素增强的AR基因mRNA水平和启动子活性。荧光素酶报告基因检测表明,启动子中的渗透反应元件对于对姜黄素的反应性至关重要。姜黄素加速了核因子红系2相关因子2(Nrf2)的核转位,并且Nrf2的过表达而非显性负性Nrf2增强了AR基因的启动子活性。用姜黄素预孵育的细胞对ROS诱导的凋亡死亡具有抗性。在存在AR抑制剂或小干扰RNA的情况下,这些作用显著减弱,表明AR对ROS诱导的细胞损伤具有保护作用。综上所述,姜黄素激活PI3K和p38 MAPK通过Nrf2增强了AR基因的表达,并且AR活性增加可能是细胞对抗氧化应激的重要反应。
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