Effects of undescribed iridoids in Patrinia punctiflora on insulin resistance in HepG2 cells

Fitoterapia. 2024 Oct:178:106160. doi: 10.1016/j.fitote.2024.106160. Epub 2024 Aug 2.

Abstract

Patrinia punctiflora is a medical and edible Chinese herb with high nutritional and medicinal value. The continuing study of its chemical constituents led to the isolation of six iridoids, which were previously unreported compounds, patriscabioins PU (1-6). Their structures were characterized and confirmed with NMR (1D & 2D), HRMS, IR and UV. Among them, compound 5 was screened to evaluate its insulin resistance activity on an IR-HepG-2 cell model. Compound 5 had no cytotoxicity compared with the control group and could promote glucose uptake in IR-HepG-2 cells. Through further mechanism studies, the undescribed compound 5 could increase the expression levels of PI-3 K, p-AKT, GLUT4 and p-GSK3β proteins. Moreover, the expression of PEPCK and G6Pase proteins, which are key gluconeogenic enzymes, was also inhibited. Thus, compound 5 promotes the transfer of GLUT4 to the plasma membrane by activating the PI-3 K/AKT signaling pathway, at the same time, promotes glycogen synthesis and inhibits the onset of gluconeogenesis, which in turn ameliorates insulin resistance.

Keywords: HepG-2 cell; Insulin resistance; Iridoid; PI-3K/AKT; Patrinia punctiflora P.S. Hsu & H. J. Wang.

MeSH terms

  • China
  • Gluconeogenesis / drug effects
  • Glucose / metabolism
  • Glucose Transporter Type 4 / metabolism
  • Hep G2 Cells
  • Humans
  • Insulin Resistance*
  • Iridoids* / chemistry
  • Iridoids* / isolation & purification
  • Iridoids* / pharmacology
  • Molecular Structure
  • Patrinia* / chemistry
  • Phosphatidylinositol 3-Kinases / metabolism
  • Phytochemicals / isolation & purification
  • Phytochemicals / pharmacology
  • Proto-Oncogene Proteins c-akt / metabolism
  • Signal Transduction / drug effects

Substances

  • Iridoids
  • Proto-Oncogene Proteins c-akt
  • Glucose Transporter Type 4
  • Phytochemicals
  • Glucose
  • Phosphatidylinositol 3-Kinases