Andrographis paniculata (Burm. f.) Nees extract ameliorates insulin resistance in the insulin-resistant HepG2 cells via GLUT2/IRS-1 pathway

Arch Physiol Biochem. 2024 Dec;130(6):779-789. doi: 10.1080/13813455.2023.2273221. Epub 2023 Oct 25.

Abstract

Hyperglycaemia is one condition related to inflammation leading to insulin signalling impairment. This study was conducted to investigate the insulin sensitivity improvement of Sambiloto (Andrographis paniculata (Burm. f.)) Nees extract in insulin resistance-induced HepG2 (IR-HepG2) cells by stimulating insulin sensitivities and inhibiting inflammatory response. Sambiloto extract at 2 µg/mL revealed glucose uptake stimulation and up-regulating GLUT-2 and IRS-1 gene expression, and inhibited pro-inflammatory cytokine IL-6 gene expression in IR-HepG2 cells. Phytochemical analysis showed that the total phenolic level and andrografolide content of Sambiloto extract were 2.91 ± 0.04% and 1.95%, respectively. This result indicated that Sambiloto extract ameliorated insulin resistance in high glucose-induced IR-HepG2 cells via modulating the IRS-1/GLUT-2 pathway due to IL-6 inhibition. These findings suggested that Sambiloto extract had potency as an anti-inflammatory and insulin-resistance improvement in IR-HepG2 cells.

Keywords: Glucose transporter 2 (GLUT-2); HepG2 cell; Sambiloto (Andrographis paniculata (Burm. f.) Nees; insulin receptor substrate 1 (IRS-1); insulin resistance.

MeSH terms

  • Andrographis* / chemistry
  • Glucose / metabolism
  • Glucose Transporter Type 2* / genetics
  • Glucose Transporter Type 2* / metabolism
  • Hep G2 Cells
  • Humans
  • Insulin / metabolism
  • Insulin Receptor Substrate Proteins* / genetics
  • Insulin Receptor Substrate Proteins* / metabolism
  • Insulin Resistance*
  • Interleukin-6* / genetics
  • Interleukin-6* / metabolism
  • Plant Extracts* / chemistry
  • Plant Extracts* / pharmacology
  • Signal Transduction* / drug effects

Substances

  • Insulin Receptor Substrate Proteins
  • Plant Extracts
  • IRS1 protein, human
  • Glucose Transporter Type 2
  • Interleukin-6
  • SLC2A2 protein, human
  • Glucose
  • IL6 protein, human
  • Insulin