Autophagy is involved in the effects of resveratrol on prevention of splenocyte apoptosis caused by oxidative stress in restrained mice

Mol Nutr Food Res. 2013 Jul;57(7):1145-57. doi: 10.1002/mnfr.201200662. Epub 2013 Mar 15.

Abstract

Scope: Resveratrol, a powerful natural compound for human health, is widely reported for its immunity-related beneficial properties. However, few works have studied its effect mechanism on immunity. The present study was conducted to investigate the effects of resveratrol on splenic immunity in restraint stressed mice and the mechanism was further studied as autophagy induction.

Methods and results: Mice were administered with resveratrol for 7 days consecutively, fixed in restraint cages for 18 h, and recovered for 12 h after the last administration. Data showed that restraint led to spleen damages, including declined spleen index, decreased CD4(+) T-cell number, increased mitochondrial oxidative damage, and apoptosis of splenocytes. Resveratrol, vitamin C (antioxidant), and rapamycin (autophagy agonist) protected spleen functions. Meanwhile, rapamycin augmented the effects of resveratrol that were abolished by chloroquine (autophagy antagonists). Further studies showed that expressions of Beclin 1 and LC3β required in autophagy development were significantly upregulated by resveratrol but not by vitamin C.

Conclusion: This study demonstrated that resveratrol preserved splenic immunity of restraint stressed mice. It is meaningful to find that autophagy, apart from reactive oxygen species clearance, is included as a potential mechanism via which resveratrol ameliorated the state of oxidative stress and thus protected splenocytes in mice.

Keywords: Autophagy; Oxidative stress; Restraint; Resveratrol; Splenocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / pharmacology
  • Apoptosis / drug effects*
  • Apoptosis Regulatory Proteins / metabolism
  • Ascorbic Acid / pharmacology
  • Autophagy / drug effects*
  • Beclin-1
  • In Situ Nick-End Labeling
  • Male
  • Membrane Potential, Mitochondrial
  • Mice
  • Microtubule-Associated Proteins / metabolism
  • Oxidative Stress / drug effects*
  • Reactive Oxygen Species / metabolism
  • Resveratrol
  • Sirolimus / pharmacology
  • Spleen / cytology
  • Spleen / drug effects*
  • Spleen / immunology
  • Stilbenes / pharmacology*
  • T-Lymphocyte Subsets / cytology
  • Up-Regulation

Substances

  • Antioxidants
  • Apoptosis Regulatory Proteins
  • Beclin-1
  • Becn1 protein, mouse
  • Map1lc3b protein, mouse
  • Microtubule-Associated Proteins
  • Reactive Oxygen Species
  • Stilbenes
  • Ascorbic Acid
  • Resveratrol
  • Sirolimus