(-)- O-Methylcubebin from Vitex trifolia Enhanced Adipogenesis in 3T3-L1 Cells via the Inhibition of ERK1/2 and p38MAPK Phosphorylation

Molecules. 2019 Dec 24;25(1):73. doi: 10.3390/molecules25010073.

Abstract

In this study, for the purpose of elucidation for antidiabetic components, we isolated and identified compounds that could become lead compounds for the development of antidiabetic agents from the herbal medicine Vitex trifolia, which is used for liver protection in Myanmar. Three kinds of lignan, (-)-O-methylcubebin (MC), (-)-hinokinin, and (-)-cubebin, were isolated from the ethyl acetate extract of the leaves of V. trifolia, using various chromatography. Among the three isolated compounds, MC showed the strongest effects to increase intracellular lipid accumulation in 3T3-L1 cells. From the results of the elucidation of the MC's effects on the adipogenesis of 3T3-L1 cells, the downsizing of adipocytes and the promotion of the expression of adipogenesis-related proteins, as well as adiponectin, were observed. On the other hand, since the activity of MC was inhibited by antagonists of PPARγ and improved by inhibitors of the classical mitogen-activated protein kinase (MAPK) pathway and p38MAPK pathway, MC was considered to be an agonist of PPARγ, and furthermore promoted adipogenesis via the inhibition of extracellular signal-regulated kinase 1/2 (ERK1/2) and p38MAPK phosphorylation. Although MC showed similar effects to those of rosiglitazone (RO) used as a positive control, RO promoted the migration of GLUT4 from the cytoplasm to the cell membrane, whereas MC did not show such an effect. From the abovementioned results, it was considered that MC could be a lead compound for the development of antidiabetic drugs that does not show weight gain, which is a side effect of RO.

Keywords: (-)-O-methylcubebin; Vitex trifolia L.; adipogenesis; lipogenesis; lipolysis; rosiglitazone.

MeSH terms

  • 3T3-L1 Cells
  • Adipogenesis / drug effects*
  • Adiponectin / metabolism
  • Animals
  • Berberine / pharmacology
  • Cell Death / drug effects
  • Cell Membrane / drug effects
  • Cell Membrane / metabolism
  • Glucose Transporter Type 4 / metabolism
  • Lignans / pharmacology*
  • Lipid Metabolism / drug effects
  • MAP Kinase Signaling System / drug effects*
  • Mice
  • PPAR gamma / antagonists & inhibitors
  • PPAR gamma / metabolism
  • Phosphorylation / drug effects
  • Plant Extracts / pharmacology
  • Protein Kinase Inhibitors / pharmacology
  • Rosiglitazone / pharmacology
  • Signal Transduction / drug effects
  • Up-Regulation / drug effects
  • Vitex / chemistry*
  • p38 Mitogen-Activated Protein Kinases / metabolism*

Substances

  • Adiponectin
  • Glucose Transporter Type 4
  • Lignans
  • PPAR gamma
  • Plant Extracts
  • Protein Kinase Inhibitors
  • Rosiglitazone
  • Berberine
  • p38 Mitogen-Activated Protein Kinases
  • cubebin