The inhibition of diacylglycerol acyltransferase by terpenoids from Youngia koidzumiana

Arch Pharm Res. 2005 Feb;28(2):164-8. doi: 10.1007/BF02977708.

Abstract

The EtOAc extract of Youngia koidzumiana significantly inhibited the diacylglycerol acyltransferase (DGAT) from rat liver microsomes. Bioactivity-guided fractionation led to the isolation of nine compounds, the structures of which were established using physicochemical and spectral data. Of the isolated compounds, oleanolic acid (2), methyl ursolate (7) and corosolic aicd (8) inhibited DGAT, with IC50 values of 31.7, 26.4, and 44.3 microM, respectively. However, sesquiterpenoids showed only weak inhibitory effects toward DGAT.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acyltransferases / antagonists & inhibitors*
  • Animals
  • Asteraceae / chemistry*
  • Chromatography, Thin Layer
  • Diacylglycerol O-Acyltransferase
  • Enzyme Inhibitors / isolation & purification
  • Enzyme Inhibitors / pharmacology*
  • In Vitro Techniques
  • Liver / drug effects
  • Liver / enzymology
  • Magnetic Resonance Spectroscopy
  • Male
  • Microsomes, Liver / drug effects
  • Microsomes, Liver / enzymology
  • Plant Extracts / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Spectrophotometry, Infrared
  • Terpenes / isolation & purification
  • Terpenes / pharmacology*

Substances

  • Enzyme Inhibitors
  • Plant Extracts
  • Terpenes
  • Acyltransferases
  • Diacylglycerol O-Acyltransferase