Leathesia difformis Extract Inhibits α-MSH-Induced Melanogenesis in B16F10 Cells via Down-Regulation of CREB Signaling Pathway

Int J Mol Sci. 2019 Jan 28;20(3):536. doi: 10.3390/ijms20030536.

Abstract

Leathesia difformis (L.) Areschoug (L. difformis) is a species of littoral brown algae of the class Phaeophyceae. Only a few studies on the apoptotic, antiviral, and antioxidant properties of L. difformis have been reported, and its inhibitory effect on melanin synthesis has not been studied. The aim of this study was to investigate the anti-melanogenic effect of L. difformis extract on α-melanocyte-stimulating hormone (α-MSH)-induced B16F10 melanocytes and its mechanism of action. L. difformis was extracted using 80% ethanol (LDE) and then fractioned between ethyl acetate (LDE-EA) and water (LDE-A). Our data demonstrated that LDE-EA significantly inhibited melanin level and cellular tyrosinase activity in α-MSH-stimulated B16 cells. In addition, the expression of genes associated with melanin synthesis, such as microphthalmia-associated transcription factor (Mitf), tyrosinase (Tyr), tyrosinase-related protein-1 (Trp-1), dopachrome tautomerase (Dct), and melanocortin 1 receptor (Mc1r) was down-regulated by LDE-EA treatment. Moreover, LDE-EA decreased p-CREB levels, which suggests that the inhibition of the cAMP/PKA/CREB pathways may be involved in the anti-melanogenic effect of LDE-EA. Thus, this study revealed that LDE-EA is an effective inhibitor of hyperpigmentation through inhibition of CREB pathways and may be considered as a potential therapeutic agent for hyperpigmentation disorders.

Keywords: B16F10; CREB pathway; Leathesia difformis; melanogenesis; tyrosinase.

MeSH terms

  • Animals
  • Cell Death / drug effects
  • Cell Survival / drug effects
  • Cyclic AMP / metabolism
  • Cyclic AMP Response Element-Binding Protein / metabolism*
  • Down-Regulation / drug effects*
  • Gene Expression Regulation, Neoplastic / drug effects
  • Melanins / biosynthesis*
  • Melanoma, Experimental / metabolism*
  • Mice
  • Models, Biological
  • Monophenol Monooxygenase / metabolism
  • Phaeophyceae / chemistry*
  • Phosphorylation / drug effects
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Reference Standards
  • Signal Transduction*
  • Xanthophylls / analysis
  • alpha-MSH / pharmacology*

Substances

  • Cyclic AMP Response Element-Binding Protein
  • Melanins
  • RNA, Messenger
  • Xanthophylls
  • fucoxanthin
  • alpha-MSH
  • Cyclic AMP
  • Monophenol Monooxygenase