Resveratrol improves oxidative stress and prevents the progression of periodontitis via the activation of the Sirt1/AMPK and the Nrf2/antioxidant defense pathways in a rat periodontitis model

Free Radic Biol Med. 2014 Oct:75:222-9. doi: 10.1016/j.freeradbiomed.2014.07.034. Epub 2014 Aug 1.

Abstract

Oxidative stress is a key factor regulating the systemic pathophysiological effects associated with periodontitis. Resveratrol is a phytochemical with antioxidant and anti-inflammatory properties that can reduce oxidative stress and inflammation. We hypothesized that resveratrol may prevent the progression of periodontitis and reduce systemic oxidative stress through the activation of the sirtuin 1 (Sirt1)/AMP-activated protein kinase (AMPK) and the nuclear factor E2-related factor 2 (Nrf2)/antioxidant defense pathways. Three groups of male Wistar rats (periodontitis treated with melinjo resveratrol, periodontitis without resveratrol, and control rats with no periodontitis or resveratrol treatment) were examined. A ligature was placed around the maxillary molars for 3 weeks to induce periodontitis, and the rats were then given drinking water with or without melinjo resveratrol. In rats with periodontitis, ligature placement induced alveolar bone resorption, quantified using three-dimensional images taken by micro-CT, and increased proinflammatory cytokine levels in gingival tissue. Melinjo resveratrol intake relieved alveolar bone resorption and activated the Sirt1/AMPK and the Nrf2/antioxidant defense pathways in inflamed gingival tissues. Further, melinjo resveratrol improved the systemic levels of 8-hydroxydeoxyguanosine, dityrosine, nitric oxide metabolism, nitrotyrosine, and proinflammatory cytokines. We conclude that oral administration of melinjo resveratrol may prevent the progression of ligature-induced periodontitis and improve systemic oxidative and nitrosative stress.

Keywords: AMPK; Cytokines; Free radicals; Nrf2; Oxidative stress; Periodontitis; Resveratrol; Sirt1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 8-Hydroxy-2'-Deoxyguanosine
  • AMP-Activated Protein Kinases / metabolism
  • Animals
  • Anti-Inflammatory Agents / pharmacology*
  • Antioxidants / pharmacology*
  • Bone Resorption / drug therapy
  • Cytokines / blood
  • Deoxyguanosine / analogs & derivatives
  • Deoxyguanosine / urine
  • Disease Models, Animal
  • Gingiva / pathology
  • Inflammation / drug therapy
  • Inflammation / prevention & control
  • Male
  • NF-E2-Related Factor 2 / metabolism
  • Nitric Oxide / blood
  • Oxidative Stress / drug effects*
  • Periodontitis / drug therapy
  • Periodontitis / prevention & control*
  • Random Allocation
  • Rats
  • Rats, Wistar
  • Resveratrol
  • Sirtuin 1 / metabolism
  • Stilbenes / pharmacology*
  • Tyrosine / analogs & derivatives
  • Tyrosine / blood
  • Tyrosine / urine

Substances

  • Anti-Inflammatory Agents
  • Antioxidants
  • Cytokines
  • NF-E2-Related Factor 2
  • Nfe2l2 protein, rat
  • Stilbenes
  • Nitric Oxide
  • 3-nitrotyrosine
  • Tyrosine
  • 8-Hydroxy-2'-Deoxyguanosine
  • dityrosine
  • AMP-Activated Protein Kinases
  • Sirt1 protein, rat
  • Sirtuin 1
  • Deoxyguanosine
  • Resveratrol