Dieckol isolated from Ecklonia cava protects against high-glucose induced damage to rat insulinoma cells by reducing oxidative stress and apoptosis

Biosci Biotechnol Biochem. 2012;76(8):1445-51. doi: 10.1271/bbb.120096. Epub 2012 Aug 7.

Abstract

Pancreatic β cells are very sensitive to oxidative stress and this might play an important role in β cell death with diabetes. The protective effect of dieckol, one of the phlorotannin polyphenol compounds purified from Ecklonia cava (E. cava), against high glucose-induced oxidative stress was investigated by using rat insulinoma cells. A high-glucose (30 mM) treatment induced the death of rat insulinoma cells, but dieckol, at a concentration 17.5 or 70 µM, significantly inhibited the high-glucose induced glucotoxicity. Treatment with dieckol also dose-dependently reduced thiobarbituric acid reactive substances (TBARS), the generation of intracellular reactive oxygen species (ROS), and the nitric oxide level increased by a high glucose concentration. In addition, the dieckol treatment increased the activities of antioxidative enzymes including catalase (CAT), superoxide dismutase (SOD) and glutathione peroxidase (GSH-px) in high glucose-pretreated rat insulinoma cells. Dieckol protected rat insulinoma cells damage under high glucose conditions. These effects were mediated by suppressing apoptosis and were associated with increased anti-apoptotic Bcl-2 expression, and reduced pro-apoptotic cleaved caspase-3 expression. These findings indicate that dieckol might be useful as a potential pharmaceutical agent to protect against the glucotoxicity caused by hyperglycemia-induced oxidative stress associated with diabetes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / isolation & purification
  • Antioxidants / pharmacology*
  • Apoptosis / drug effects
  • Benzofurans / isolation & purification
  • Benzofurans / pharmacology*
  • Caspase 3 / genetics
  • Caspase 3 / metabolism
  • Catalase / genetics
  • Catalase / metabolism
  • Dose-Response Relationship, Drug
  • Gene Expression / drug effects
  • Glucose / adverse effects
  • Glutathione Peroxidase / genetics
  • Glutathione Peroxidase / metabolism
  • Insulinoma / metabolism
  • Insulinoma / pathology
  • Nitric Oxide / antagonists & inhibitors
  • Nitric Oxide / biosynthesis
  • Oxidative Stress / drug effects
  • Phaeophyceae / chemistry*
  • Proto-Oncogene Proteins c-bcl-2 / genetics
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Rats
  • Reactive Oxygen Species / antagonists & inhibitors*
  • Reactive Oxygen Species / metabolism
  • Superoxide Dismutase / genetics
  • Superoxide Dismutase / metabolism
  • Thiobarbituric Acid Reactive Substances / metabolism
  • Tumor Cells, Cultured

Substances

  • Antioxidants
  • Benzofurans
  • Proto-Oncogene Proteins c-bcl-2
  • Reactive Oxygen Species
  • Thiobarbituric Acid Reactive Substances
  • dieckol
  • Nitric Oxide
  • Catalase
  • Glutathione Peroxidase
  • Superoxide Dismutase
  • Caspase 3
  • Glucose