The protective effects of sciadopitysin against methylglyoxal-induced cytotoxicity in cultured pancreatic β-cells

J Appl Toxicol. 2018 Aug;38(8):1104-1111. doi: 10.1002/jat.3620. Epub 2018 Mar 30.

Abstract

Increased glycation of macromolecules via the reactive dicarbonyl and α-oxoaldehyde methylglyoxal (MG) has shown an association with diabetes and its complications. In the present study, the protective effects of sciadopitysin against MG-induced oxidative cell damage were investigated in the insulin-producing pancreatic β-cell line, RIN-m5F cells. When exposed to MG for 48 hours, RIN-m5F cells experienced significant loss of viability and impaired insulin secretion; however, treatment with sciadopitysin protected RIN-m5F cells against MG-induced cell death and decreased insulin secretion. Treatment of RIN-m5F cells with sciadopitysin prevented MG-induced production of interleukin-1β, intracellular reactive oxygen species and cardiolipin peroxidation. Furthermore, sciadopitysin increased adenosine monophosphate-activated protein kinase phosphorylation of RIN-m5F cells. Treatment of cells with sciadopitysin increased the activity of glyoxalase I and decreased the levels of MG-protein adducts, indicating that sciadopitysin protects against MG-induced protein glycation by increasing MG detoxification. Taken together, the results indicated the potential utility of sciadopitysin as an intervention against MG-induced cell damage in pancreatic β-cells.

Keywords: Sciadopitysin; methylglyoxal; mitochondrial biogenesis; oxidative stress; pancreatic beta cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biflavonoids / pharmacology*
  • Cardiolipins / metabolism
  • Cell Culture Techniques
  • Cell Line
  • Cell Survival / drug effects
  • Insulin / metabolism
  • Insulin-Secreting Cells / drug effects*
  • Insulin-Secreting Cells / metabolism
  • Insulin-Secreting Cells / pathology
  • Lipid Peroxidation / drug effects
  • Oxidative Stress / drug effects*
  • Protective Agents / pharmacology*
  • Pyruvaldehyde / toxicity*
  • Rats
  • Reactive Oxygen Species / metabolism

Substances

  • Biflavonoids
  • Cardiolipins
  • Insulin
  • Protective Agents
  • Reactive Oxygen Species
  • sciadopitysin
  • Pyruvaldehyde