Resveratrol protects against methylglyoxal-induced hyperglycemia and pancreatic damage in vivo

Nutrients. 2015 Apr 15;7(4):2850-65. doi: 10.3390/nu7042850.

Abstract

Methylglyoxal (MG) has been found to cause inflammation and insulin resistance in vitro and in vivo in recent studies. Resveratrol has been proposed as an effective treatment that helps lower the risk of developing complications of diabetes. To study the significance of glycosylation-related stress on the pathology of diabetes, the effects of resveratrol were examined in a mouse model of diabetes induced by MG. Resveratrol was given via oral gavage in MG-treated mice, and diabetes-related tests and markers were assessed using biochemical and immunohistochemical analyses. Treatment with resveratrol markedly improved blood glucose level from the oral glucose tolerance test and promoted nuclear factor erythroid 2-related factor-2 (Nrf2) phosphorylation (p < 0.05) in the pancreas of MG-treated mice. However, these effects were abolished by retinoic acid, Nrf2 inhibitor, in resveratrol and retinoic acid-treated and MG-induced mice. These findings support that resveratrol may be useful in the treatment of type-2 diabetes by protecting against pancreatic cell dysfunction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / pharmacology
  • Blood Glucose / metabolism
  • Disease Models, Animal
  • Glucose Tolerance Test
  • Hyperglycemia / chemically induced
  • Hyperglycemia / drug therapy*
  • Hypoglycemic Agents / pharmacology
  • Inflammation / chemically induced
  • Inflammation / drug therapy
  • Insulin / blood
  • Insulin Receptor Substrate Proteins / genetics
  • Insulin Receptor Substrate Proteins / metabolism
  • Insulin Resistance
  • Liver / drug effects
  • Liver / metabolism
  • Male
  • Mice
  • Mice, Inbred BALB C
  • NF-E2-Related Factor 2 / genetics
  • NF-E2-Related Factor 2 / metabolism
  • Pancreas / cytology
  • Pancreas / drug effects
  • Pancreas / metabolism
  • Pancreatic Diseases / chemically induced
  • Pancreatic Diseases / drug therapy*
  • Phosphorylation
  • Pyruvaldehyde / adverse effects*
  • Resveratrol
  • Stilbenes / pharmacology*

Substances

  • Anti-Inflammatory Agents
  • Blood Glucose
  • Hypoglycemic Agents
  • Insulin
  • Insulin Receptor Substrate Proteins
  • Irs1 protein, mouse
  • NF-E2-Related Factor 2
  • Nfe2l2 protein, mouse
  • Stilbenes
  • Pyruvaldehyde
  • Resveratrol