Hypo-pigmenting effect of sesquiterpenes from Inula britannica in B16 melanoma cells

Arch Pharm Res. 2014 May;37(5):567-74. doi: 10.1007/s12272-013-0302-4. Epub 2013 Dec 18.

Abstract

During the course of screens to identify anti-melanogenic agents from natural resources, we found that the methanol extract of the dried flower of Inula britannica L. inhibited melanin synthesis in cultured melanoma cells stimulated with 3-isobutyl-1-methylxanthine (IBMX). A bioassay-guided isolation of the chloroform fraction of the I. britannica using an in vitro melanogenesis inhibition assay led to the isolation of sesquiterpenes, 1-O-acetylbritannilactone (1), britannilactone (2) and neobritannilactone B (3). Compounds 1 and 2 significantly reduced melanin production in a dose-dependent manner with IC50 values of 13.3 and 15.5 μM, respectively, whereas compound 3 was found to be cytotoxic. Compound 1 also inhibited the tyrosinase activity only in cell based-systems. Western blot analysis indicated that compound 1 inhibited melanogenesis by activating extracellular signal-regulated kinase (ERK) and Akt signaling and also inhibiting cAMP related binding protein, which regulates its downstream pathway, including tyrosinase, tyrosinase related protein-1 and TRP-2. These results demonstrated that compound 1, a major sesquiterpene from the flowers of I. britannica, exhibited anti-melanogenic activity by suppression of tyrosinase expression via ERK and Akt signaling. Taken together, our results suggest that these compounds may act as potent natural skin-lightening agents.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Cyclic AMP Response Element-Binding Protein / metabolism
  • Dose-Response Relationship, Drug
  • Extracellular Signal-Regulated MAP Kinases / antagonists & inhibitors
  • Extracellular Signal-Regulated MAP Kinases / metabolism
  • Flowers
  • Inula* / chemistry
  • Melanins / biosynthesis*
  • Melanoma, Experimental / metabolism*
  • Mice
  • Monophenol Monooxygenase / metabolism
  • Phytotherapy
  • Pigmentation / drug effects*
  • Plant Extracts / isolation & purification
  • Plant Extracts / pharmacology*
  • Plants, Medicinal
  • Protein Kinase Inhibitors / pharmacology
  • Proto-Oncogene Proteins c-akt / antagonists & inhibitors
  • Proto-Oncogene Proteins c-akt / metabolism
  • Sesquiterpenes / isolation & purification
  • Sesquiterpenes / pharmacology*
  • Signal Transduction / drug effects
  • Skin Lightening Preparations / isolation & purification
  • Skin Lightening Preparations / pharmacology*

Substances

  • Creb1 protein, mouse
  • Cyclic AMP Response Element-Binding Protein
  • Melanins
  • Plant Extracts
  • Protein Kinase Inhibitors
  • Sesquiterpenes
  • Skin Lightening Preparations
  • Monophenol Monooxygenase
  • Proto-Oncogene Proteins c-akt
  • Extracellular Signal-Regulated MAP Kinases