Z-Ligustilide inhibits benzo(a)pyrene-induced CYP1A1 upregulation in cultured human keratinocytes via ROS-dependent Nrf2 activation

Exp Dermatol. 2014 Apr;23(4):260-5. doi: 10.1111/exd.12360.

Abstract

Benzo(a)pyrene (BaP), a polycyclic aromatic hydrocarbon (PAH), is an environmental contaminant that can induce cytochrome P4501A1 (CYP1A1) upregulation via aryl hydrocarbon receptor (AhR) activation and provoke inflammation. Here, we investigated the effect of Z-Ligustilide, an active ingredient isolated from the medicinal plants Cnidium officinale and Angelica acutiloba, on BaP-induced CYP1A1 upregulation in normal human epidermal keratinocytes (NHEKs) as well as its underlying mechanisms. Z-Ligustilide significantly inhibited BaP-induced CYP1A1 upregulation in NHEKs. Treatment of NHEKs with Z-Ligustilide induced Nuclear factor-E2-related factor 2 (Nrf2) nuclear translocation and expression of the Nrf2-regulated genes for haeme oxygenase-1 (HO-1) and

Nad(p)h: quinine oxidoreductase-1 (NQO1). AhR silencing, SB203580 (a p38 inhibitor), SP600125 (a JNK inhibitor), U0126 (a MEK inhibitor) and LY294002 (a PI3K inhibitor) did not suppress Z-Ligustilide-induced Nrf2 activation. Moreover, treatment of NHEKs with Z-Ligustilide increased reactive oxygen species (ROS) and L-N-acetylcysteine (L-NAC, an antioxidant) attenuated Z-ligustilide-induced Nrf2 nuclear translocation and HO-1 expression. L-NAC or knock-down of Nrf2 significantly attenuated the inhibitory effects of Z-Ligustilide on BaP-induced CYP1A1 upregulation in NHEKs. Taken together, these findings suggest that Z-Ligustilide can suppress BaP-induced CYP1A1 upregulation through ROS-dependent Nrf2 pathway activation and may be beneficial in preventing or treating BaP-induced skin damage.

Keywords: Nrf2; aryl hydrocarbon receptor; cytochrome P450; keratinocytes; polycyclic aromatic hydrocarbon.

MeSH terms

  • 4-Butyrolactone / analogs & derivatives*
  • 4-Butyrolactone / pharmacology
  • 4-Butyrolactone / therapeutic use
  • Angelica
  • Benzo(a)pyrene / toxicity
  • Cell Survival / drug effects
  • Cells, Cultured
  • Cnidium
  • Cytochrome P-450 CYP1A1 / metabolism*
  • Dermatitis / etiology
  • Dermatitis / prevention & control*
  • Drug Evaluation, Preclinical
  • Environmental Pollutants / toxicity
  • Humans
  • Keratinocytes / drug effects*
  • Keratinocytes / metabolism
  • NF-E2-Related Factor 2 / metabolism*
  • Phytotherapy
  • Plant Extracts / therapeutic use
  • Reactive Oxygen Species / metabolism
  • Receptors, Aryl Hydrocarbon / metabolism
  • Up-Regulation / drug effects

Substances

  • Environmental Pollutants
  • NF-E2-Related Factor 2
  • NFE2L2 protein, human
  • Plant Extracts
  • Reactive Oxygen Species
  • Receptors, Aryl Hydrocarbon
  • Benzo(a)pyrene
  • ligustilide
  • CYP1A1 protein, human
  • Cytochrome P-450 CYP1A1
  • 4-Butyrolactone