Defensive Properties of Ginsenoside Re against UV-B-Induced Oxidative Stress through Up-Regulating Glutathione and Superoxide Dismutase in HaCaT Keratinocytes

Authors

  • Chang-Jin Lim Department of Biochemistry, College of Natural Sciences, Kangwon National University, Chuncheon 24341, Korea.
  • Dae-Duk Kim College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul 08826, Korea.
  • Daehyun Shin Research and Development Center, Cosmocos Corporation, Incheon 21698, Korea.
  • Hee Won Moon Department of Biochemistry, College of Natural Sciences, Kangwon National University, Chuncheon 24341, Korea.
  • Kyunghoon Kim Department of Biological Sciences, College of Natural Sciences, Kangwon National University, Chuncheon 24341, Korea.
  • Yuri Oh Department of Biological Sciences, College of Natural Sciences, Kangwon National University, Chuncheon 24341, Korea.
Abstract:

Ginseng is now used worldwide as a traditional Oriental medicine. Ginsenosides, alsoknown as ginseng saponins, are responsible for most pharmacological efficacies of ginseng.This work aimed to assess the novel skin anti-photoaging potential of ginsenoside Re (Re), aprotopanaxatriol-type ginsenoside, by analyzing reactive oxygen species (ROS), pro-matrixmetalloproteinase-2 (proMMP-2) and -9 (proMMP-9), total glutathione (GSH), superoxidedismutase (SOD), and cellular viability in UV-B-irradiated HaCaT keratinocytes. When HaCaTcells were pretreated with Re prior to UV-B irradiation, Re significantly suppressed the UVB-induced ROS elevation. It was also able to attenuate the UV-B-induced proMMP-2 and -9elevations at both activity and protein levels. Re was capable of overcoming the UV-B-reducedtotal GSH content and SOD activity in concentration-dependent ways. Under the experimentalconditions used, Re could interfere with cellular viabilities in neither non-irradiated nor UV-Birradiatedkeratinocytes.

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Journal title

volume 17  issue 1

pages  249- 260

publication date 2018-01-01

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