Eckol inhibits ultraviolet B-induced cell damage in human keratinocytes via a decrease in oxidative stress

Biol Pharm Bull. 2012;35(6):873-80. doi: 10.1248/bpb.35.873.

Abstract

In previous reports, the antioxidant effects of eckol were shown to protect cells against hydrogen peroxide- and gamma ray-induced oxidative stress. In this study, the role of eckol in protecting human skin keratinocytes (HaCaT) against UVB-induced oxidative cell damage was investigated. Also, triphlorethol-A, one of the chemical components in Ecklonia cava, and quercetin a well known antioxidant, were compared with eckol in terms of antioxidant activity based on chemical structure. Eckol decreased UVB-induced intracellular reactive oxygen species (ROS), decreased injury to cellular components resulting from UVB-induced oxidative stress, and restored cell viability. In addition, eckol reduced UVB-induced apoptosis by inhibiting the disruption of mitochondrial membranes. These results suggest that eckol protects human keratinocytes against UVB-induced oxidative stress by scavenging ROS, thereby lessening injury to cellular components.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antioxidants / pharmacology*
  • Cell Line
  • Cell Survival / drug effects
  • DNA Fragmentation
  • Dioxins / pharmacology*
  • Guanine / analogs & derivatives
  • Guanine / metabolism
  • Humans
  • Keratinocytes / drug effects*
  • Keratinocytes / physiology
  • Keratinocytes / radiation effects
  • Lipid Peroxidation / drug effects
  • Membrane Potential, Mitochondrial / drug effects
  • Oxidative Stress / drug effects*
  • Ultraviolet Rays / adverse effects*

Substances

  • Antioxidants
  • Dioxins
  • 8-hydroxyguanine
  • Guanine
  • eckol