Synthesis of natural 3'-Prenylchalconaringenin and biological evaluation of ameliorating non-alcoholic fatty liver disease and metabolic syndrome

Eur J Med Chem. 2020 Nov 1:205:112649. doi: 10.1016/j.ejmech.2020.112649. Epub 2020 Jul 28.

Abstract

Non-alcoholic fatty liver disease (NAFLD) is the most common cause of chronic liver disease and important risk factor for cardiac diseases, diabetes and extrahepatic cancers. Natural 3'-geranylchalconaringenin (GC) and desmethylxanthohumol (DX) from hop were synthesized using a regio-selective iodination and the Suzuki coupling reaction as key steps. GC and DX, along with their aglycone naringenin chalcone (NC) were investigated their decreasing the accumulation of cellular lipids. GC reduced lipid content and activated the AMP-activated protein kinase (AMPK) pathway in HepG2 and 3T3-L1 cells. In addition, GC had an obvious therapeutic effect on alleviating NAFLD and metabolic syndrome by activating the AMPK pathway in vivo. In conclusion, GC may be potentially used as a candidate drug and functional food for treating NAFLD and metabolic syndrome.

Keywords: 3′-Geranylchalconaringenin; AMPK pathway; Non-alcoholic fatty liver disease.

MeSH terms

  • 3T3-L1 Cells
  • AMP-Activated Protein Kinases / metabolism
  • Animals
  • Chalcones / chemical synthesis*
  • Chalcones / chemistry
  • Chalcones / pharmacology*
  • Chalcones / therapeutic use
  • Chemistry Techniques, Synthetic
  • Hep G2 Cells
  • Humans
  • Metabolic Syndrome / drug therapy*
  • Mice
  • Non-alcoholic Fatty Liver Disease / drug therapy*
  • Signal Transduction / drug effects
  • Stereoisomerism

Substances

  • Chalcones
  • naringenin chalcone
  • AMP-Activated Protein Kinases