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Up-regulation of aldose reductase expression mediated by phosphatidylinositol 3-kinase/Akt and Nrf2 is involved in the protective effect of curcumin against oxidative damage

Authors
Kang, Eun SilWoo, Im SunKim, Hyo JungEun, So YoungPaek, Kyung ShinKim, Hye JungChang, Ki ChurlLee, Jae HeunLee, Hoon TaekKim, Jin-HoiNishinaka, ToruYabe-Nishimura, ChihiroSeo, Han Geuk
Issue Date
15-Aug-2007
Publisher
ELSEVIER SCIENCE INC
Keywords
aldose reductase; curcumin; Nrf2; PI3K; MAPK; oxidative stress; apoptosis; vascular smooth muscle cells; free radicals
Citation
FREE RADICAL BIOLOGY AND MEDICINE, v.43, no.4, pp.535 - 545
Indexed
SCIE
SCOPUS
Journal Title
FREE RADICAL BIOLOGY AND MEDICINE
Volume
43
Number
4
Start Page
535
End Page
545
URI
https://scholarworks.bwise.kr/gnu/handle/sw.gnu/28307
DOI
10.1016/j.freeradbiomed.2007.05.006
ISSN
0891-5849
Abstract
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. (c) 2007 Elsevier Inc. All rights reserved.
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