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

Free Radic Biol Med. 2007 Aug 15;43(4):535-45. doi: 10.1016/j.freeradbiomed.2007.05.006. Epub 2007 May 16.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aldehyde Reductase / biosynthesis*
  • Aldehyde Reductase / drug effects
  • Aldehyde Reductase / genetics
  • Animals
  • Antioxidants / pharmacology*
  • Apoptosis / drug effects
  • Blotting, Northern
  • Blotting, Western
  • Cells, Cultured
  • Curcumin / pharmacology*
  • Dose-Response Relationship, Drug
  • Gene Expression / drug effects
  • Gene Expression Regulation, Enzymologic / drug effects*
  • In Situ Nick-End Labeling
  • Microscopy, Confocal
  • Muscle, Smooth, Vascular / drug effects
  • Muscle, Smooth, Vascular / metabolism
  • Mutagenesis, Site-Directed
  • NF-E2-Related Factor 2 / metabolism*
  • Oncogene Protein v-akt / metabolism
  • Oxidative Stress / drug effects
  • Oxidative Stress / physiology
  • Phosphatidylinositol 3-Kinases / drug effects
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Promoter Regions, Genetic
  • RNA, Messenger / analysis
  • RNA, Small Interfering
  • Rats
  • Reactive Oxygen Species / metabolism
  • Up-Regulation
  • p38 Mitogen-Activated Protein Kinases / drug effects
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Antioxidants
  • NF-E2-Related Factor 2
  • RNA, Messenger
  • RNA, Small Interfering
  • Reactive Oxygen Species
  • Aldehyde Reductase
  • Phosphatidylinositol 3-Kinases
  • Oncogene Protein v-akt
  • p38 Mitogen-Activated Protein Kinases
  • Curcumin