Anti-melanogenic effects of resveratryl triglycolate, a novel hybrid compound derived by esterification of resveratrol with glycolic acid

Arch Dermatol Res. 2016 Jul;308(5):325-34. doi: 10.1007/s00403-016-1644-9. Epub 2016 Apr 8.

Abstract

Resveratrol is known to inhibit cellular melanin synthesis by multiple mechanisms. Glycolic acid (GA) is used in skin care products for its excellent skin penetration. The purpose of this study was to examine the anti-melanogenic effects of resveratryl triglycolate (RTG), a novel hybrid compound of resveratrol and GA, in comparison with resveratrol, GA, resveratryl triacetate (RTA) and arbutin. Resveratrol, RTG, and RTA inhibited the catalytic activity human tyrosinase (TYR) more potently than arbutin or GA did. Their cytotoxic and anti-melanogenic effects were examined using murine melanoma B16/F10 cells and human epidermal melanocytes (HEMs). The cytotoxicity of RTG was similar to that of resveratrol and RTA. RTG at 3-10 μM decreased melanin levels and cellular TYR activities in α-melanocyte-stimulating hormone-stimulated B16/F10 cells, and L-tyrosine-stimulated HEMs. RTG also suppressed mRNA and protein expression of TYR, tyrosinase-related protein 1, L-3,4-dihydroxyphenylalanine chrome tautomerase, and microphthalmia-associated transcription factor (MITF) in HEMs stimulated with L-tyrosine. This study suggests that, like resveratrol and RTA, RTG can attenuate cellular melanin synthesis effectively through the suppression of MITF-dependent expression of melanogenic enzymes and the inhibition of catalytic activity of TYR enzyme. RTG therefore has potential for use as a cosmeceutical ingredient for skin whitening.

Keywords: Glycolic acid; Melanin; Resveratrol; Resveratryl triglycolate.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Arbutin / pharmacology
  • Cell Culture Techniques
  • Cell Line, Tumor
  • Enzyme Inhibitors / pharmacology*
  • Epidermal Cells
  • Esterification
  • Glycolates / pharmacology*
  • Humans
  • Intramolecular Oxidoreductases / metabolism
  • Keratolytic Agents / pharmacology*
  • Melanins / metabolism*
  • Melanocytes / drug effects*
  • Melanocytes / metabolism
  • Membrane Glycoproteins
  • Mice
  • Microphthalmia-Associated Transcription Factor / metabolism
  • Monophenol Monooxygenase / antagonists & inhibitors*
  • Oxidoreductases
  • Resveratrol
  • Stilbenes / pharmacology*
  • alpha-MSH / pharmacology

Substances

  • Enzyme Inhibitors
  • Glycolates
  • Keratolytic Agents
  • MITF protein, human
  • Melanins
  • Membrane Glycoproteins
  • Microphthalmia-Associated Transcription Factor
  • Stilbenes
  • resveratryl triacetate
  • glycolic acid
  • alpha-MSH
  • Arbutin
  • Oxidoreductases
  • TYRP1 protein, human
  • Monophenol Monooxygenase
  • Intramolecular Oxidoreductases
  • dopachrome isomerase
  • Resveratrol