β-Sitosterol-D-Glucopyranoside Mimics Estrogenic Properties and Stimulates Glucose Utilization in Skeletal Muscle Cells

Molecules. 2021 May 24;26(11):3129. doi: 10.3390/molecules26113129.

Abstract

Estrogenic molecules have been reported to regulate glucose homeostasis and may be beneficial for diabetes management. Here, we investigated the estrogenic effect of β-sitosterol-3-O-D-glucopyranoside (BSD), isolated from the fruits of Cupressus sempervirens and monitored its ability to regulate glucose utilization in skeletal muscle cells. BSD stimulated ERE-mediated luciferase activity in both ERα and ERβ-ERE luc expression system with greater response through ERβ in HEK-293T cells, and induced the expression of estrogen-regulated genes in estrogen responsive MCF-7 cells. In silico docking and molecular interaction studies revealed the affinity and interaction of BSD with ERβ through hydrophobic interaction and hydrogen bond pairing. Furthermore, prolonged exposure of L6-GLUT4myc myotubes to BSD raised the glucose uptake under basal conditions without affecting the insulin-stimulated glucose uptake, the effect associated with enhanced translocation of GLUT4 to the cell periphery. The BSD-mediated biological response to increase GLUT4 translocation was obliterated by PI-3-K inhibitor wortmannin, and BSD significantly increased the phosphorylation of AKT (Ser-473). Moreover, BSD-induced GLUT4 translocation was prevented in the presence of fulvestrant. Our findings reveal the estrogenic activity of BSD to stimulate glucose utilization in skeletal muscle cells via PI-3K/AKT-dependent mechanism.

Keywords: Cupressus sempervirens; glucose uptake; insulin resistance; phytoestrogen; skeletal muscle.

MeSH terms

  • Glucose / metabolism*
  • Glucose Transporter Type 4 / metabolism
  • HEK293 Cells
  • Humans
  • MCF-7 Cells
  • Magnetic Resonance Spectroscopy
  • Mass Spectrometry
  • Molecular Mimicry*
  • Muscle, Skeletal / cytology
  • Muscle, Skeletal / metabolism*
  • Phosphatidylinositol 3-Kinases / metabolism
  • Phytoestrogens / pharmacology*
  • Proto-Oncogene Proteins c-akt / metabolism
  • Signal Transduction
  • Sitosterols / chemistry
  • Sitosterols / pharmacology*

Substances

  • Glucose Transporter Type 4
  • Phytoestrogens
  • SLC2A4 protein, human
  • Sitosterols
  • gamma-sitosterol
  • Proto-Oncogene Proteins c-akt
  • Glucose