The alpha-methylene-gamma-butyrolactone moiety in dehydrocostus lactone is responsible for cytoprotective heme oxygenase-1 expression through activation of the nuclear factor E2-related factor 2 in HepG2 cells

Eur J Pharmacol. 2007 Jun 22;565(1-3):37-44. doi: 10.1016/j.ejphar.2007.02.053. Epub 2007 Mar 7.

Abstract

Inducible heme oxygenase (HO)-1 acts against oxidants that are thought to play a major role in the pathogenesis of several diseases. The alpha-methylene-gamma-butyrolactone (CH2-BL) structural unit, which characterizes a group of naturally occurring sesquiterpene lactones, is known to possess numerous biological activities. In the present study, we evaluated dehydrocostus lactone possessing CH2-BL moiety, one of the bioactive constituents of the medicinal plant Saussurea lappa, as an inducer of cytoprotective HO-1. In HepG2 cells, treatment with dehydrocostus lactone induced HO-1 expression and increased HO activity in a concentration-dependent manner. Similar results were also observed when the cells were incubated with CH2-BL, a parent structure of dehydrocostus lactone. In contrast, mokko lactone, a reduced product of dehydrocostus lactone, and alpha-methyl-gamma-butyrolactone (CH3-BL), a parent structure of mokko lactone, did not induce HO-1 expression. Pretreatment with either dehydrocostus lactone or CH2-BL for 6 h protected the cells from hydrogen peroxide-mediated toxicity, whereas mokko lactone or CH3-BL failed to exert a cytoprotective action. Inhibition of HO-1 expression by HO-1 small interfering RNA (siRNA) abrogated cellular protection afforded by dehydrocostus lactone or CH2-BL. In addition, dehydrocostus lactone caused the nuclear accumulation of the nuclear factor E2-related factor 2 (Nrf2) and increased the promoter activity of antioxidant response element (ARE). Using Nrf2 siRNA, Nrf2 activation was confirmed to contribute to cytoprotective HO-1 expression by dehydrocostus lactone or CH2-BL. Collectively, our findings suggest that CH2-BL moiety in dehydrocostus lactone increases cellular resistance to oxidant injury in HepG2 cells, presumably through Nrf2/ARE-dependent HO-1 expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 4-Butyrolactone / analogs & derivatives*
  • 4-Butyrolactone / pharmacology
  • Active Transport, Cell Nucleus
  • Antioxidants / pharmacology*
  • Cell Line
  • Cytoprotection*
  • Heme Oxygenase-1 / genetics
  • Heme Oxygenase-1 / physiology*
  • Humans
  • Lactones / chemistry
  • Lactones / pharmacology*
  • NF-E2-Related Factor 2 / physiology*
  • Response Elements / physiology
  • Sesquiterpenes / chemistry
  • Sesquiterpenes / pharmacology*

Substances

  • Antioxidants
  • Lactones
  • NF-E2-Related Factor 2
  • NFE2L2 protein, human
  • Sesquiterpenes
  • mokko lactone
  • alpha-methylene gamma-butyrolactone
  • dehydrocostus lactone
  • Heme Oxygenase-1
  • 4-Butyrolactone