[8]-Gingerol inhibits melanogenesis in murine melanoma cells through down-regulation of the MAPK and PKA signal pathways

Biochem Biophys Res Commun. 2013 Aug 23;438(2):375-81. doi: 10.1016/j.bbrc.2013.07.079. Epub 2013 Jul 25.

Abstract

[8]-Gingerol is an active component of Zinger and shows several pharmacological activities, such as antipyretic and anti-inflammation characteristics. To identify a potential skin-whitening agent, the inhibitory effects of [8]-gingerol on melanogenesis and its mechanism of action were investigated. In the present study, the effects of [8]-gingerol on mushroom tyrosinase, tyrosinase activity and melanin content were determined spectrophotometrically; the expression of melanogenesis-related proteins in B16F10 and B16F1 melanoma cells were determined by Western blotting. Furthermore, the possible signaling pathways involved in [8]-gingerol-mediated depigmentation were also investigated using specific inhibitors. The results revealed that [8]-gingerol (5-100μM) effectively suppressed intracellular tyrosinase activity and decreased the amount of melanin in B16F10 and B16F1 cells. In addition, [8]-gingerol also effectively decreased intracellular reactive species (RS) and reactive oxygen species (ROS) levels at the same dose range. Our results indicated that [8]-gingerol inhibited melanogenesis in B16F10 and B16F1 cells by down-regulation of both mitogen-activated protein kinases (MAPK) and protein kinase A (PKA) signaling pathways or through its antioxidant properties. Hence, [8]-gingerol could be used as an effective skin-whitening agent.

Keywords: Melanin; Melanogenesis; Tyrosinase; [8]-Gingerol.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Catechols / pharmacology*
  • Cell Line, Tumor
  • Cell Survival
  • Cyclic AMP-Dependent Protein Kinases / metabolism*
  • Down-Regulation
  • Fatty Alcohols / pharmacology*
  • Gene Expression Regulation, Enzymologic
  • Intramolecular Oxidoreductases / antagonists & inhibitors
  • MAP Kinase Signaling System*
  • Melanins / biosynthesis*
  • Melanoma / metabolism*
  • Melanoma, Experimental
  • Mice
  • Microphthalmia-Associated Transcription Factor / antagonists & inhibitors
  • Monophenol Monooxygenase / antagonists & inhibitors
  • Monophenol Monooxygenase / metabolism*
  • Reactive Oxygen Species
  • Receptor, Melanocortin, Type 1 / antagonists & inhibitors
  • Signal Transduction

Substances

  • Catechols
  • Fatty Alcohols
  • Melanins
  • Microphthalmia-Associated Transcription Factor
  • Mitf protein, mouse
  • Reactive Oxygen Species
  • Receptor, Melanocortin, Type 1
  • gingerol
  • Monophenol Monooxygenase
  • Cyclic AMP-Dependent Protein Kinases
  • Intramolecular Oxidoreductases
  • dopachrome isomerase