Daidzein promotes glucose uptake through glucose transporter 4 translocation to plasma membrane in L6 myocytes and improves glucose homeostasis in Type 2 diabetic model mice

J Nutr Biochem. 2014 Feb;25(2):136-43. doi: 10.1016/j.jnutbio.2013.09.012. Epub 2013 Nov 6.

Abstract

Daidzein shows estrogenic, antioxidant and antiandrogenic properties as well as cell cycle regulatory activity. However, the antihyperglycemic effect of daidzein remains to be elucidated. In this study, we investigated the in vitro effect of daidzein on glucose uptake, AMPK phosphorylation and GLUT4 translocation on plasma membrane in L6 myotubes and its in vivo antihyperglycmic effect in obese-diabetic model db/db mice. Daidzein was found to promote glucose uptake, AMPK phosphorylation and GLUT4 translocation by Western blotting analyses in L6 myotubes under a condition of insulin absence. Promotion by daidzein of glucose uptake as well as GLUT4 translocation to plasma membrane by immunocytochemistry was also demonstrated in L6 myoblasts transfected with a GLUT4 cDNA-coding vector. Daidzein (0.1% in the diet) suppressed the rises in the fasting blood glucose, serum total cholesterol levels and homeostasis model assessment index of db/db mice. In addition, daidzein supplementation markedly improved the AMPK phosphorylation in gastrocnemius muscle of db/db mice. Daidzein also suppressed increases in blood glucose levels and urinary glucose excretion in KK-Ay mice, another Type 2 diabetic animal model. These in vitro and in vivo findings suggest that daidzein is preventive for Type 2 diabetes and an antidiabetic phytochemical.

Keywords: AMP-activated protein kinase; AMPK; Daidzein; GLUT4; Glucose transporter 4; Glucose uptake; L6 myocytes; glucose transporter 4..

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenylate Kinase / metabolism
  • Animals
  • Base Sequence
  • Cell Membrane / drug effects
  • Cell Membrane / metabolism
  • DNA Primers
  • Diabetes Mellitus, Type 2 / metabolism*
  • Glucose / metabolism*
  • Glucose Transporter Type 4 / metabolism*
  • Isoflavones / pharmacology*
  • Mice
  • Muscle Cells / drug effects*
  • Muscle Cells / metabolism
  • Phosphorylation
  • Protein Transport

Substances

  • DNA Primers
  • Glucose Transporter Type 4
  • Isoflavones
  • Slc2a4 protein, mouse
  • daidzein
  • Adenylate Kinase
  • Glucose