Comparative Study of the Effects of Light Controlled Germination Conditions on Saponarin Content in Barley Sprouts and Lipid Accumulation Suppression in HepG2 Hepatocyte and 3T3-L1 Adipocyte Cells Using Barley Sprout Extracts

Molecules. 2020 Nov 16;25(22):5349. doi: 10.3390/molecules25225349.

Abstract

Barley sprouts (BS) contain physiologically active substances and promote various positive physiological functions in the human body. The levels of the physiologically active substances in plants depend on their growth conditions. In this study, BS were germinated using differently colored LED lights and different nutrient supplements. Overall, there were 238 varied BS samples analyzed for their total polyphenol and flavonoid contents. Principal component analysis (PCA) was performed to determine the relationship between the germinated samples and their total polyphenol and flavonoid contents, and those with high levels were further analyzed for their saponarin content. Based on the PCA plot, the optimal conditions for metabolite production were blue light with 0.1% boric acid supplementation. In vitro experiments using the ethanol extract from the BS cultured in blue light showed that the extract significantly inhibited the total lipid accumulation in 3T3-L1 adipocytes and the lipid droplets in HepG2 hepatocytes. These findings suggest that specific and controlled light source and nutrient conditions for BS growth could increase the production of secondary metabolites associated with inhibited fat accumulation in adipocytes and hepatocytes.

Keywords: barley sprout; flavonoids; germination conditions; lipid accumulation; polyphenol.

Publication types

  • Comparative Study

MeSH terms

  • 3T3-L1 Cells
  • Adipocytes / drug effects
  • Adipocytes / metabolism*
  • Animals
  • Apigenin / analysis*
  • Apigenin / chemistry
  • Apigenin / pharmacology
  • Flavonoids / analysis
  • Germination / radiation effects*
  • Glucosides / analysis*
  • Glucosides / chemistry
  • Glucosides / pharmacology
  • Hepatocytes / drug effects
  • Hepatocytes / metabolism*
  • Hordeum / chemistry*
  • Hordeum / radiation effects
  • Light*
  • Lipid Metabolism / radiation effects*
  • Mice
  • Plant Extracts / pharmacology*
  • Polyphenols / analysis
  • Principal Component Analysis

Substances

  • Flavonoids
  • Glucosides
  • Plant Extracts
  • Polyphenols
  • saponarin
  • Apigenin