Resveratrol attenuates lipopolysaccharide-induced acute kidney injury by suppressing inflammation driven by macrophages

Mol Nutr Food Res. 2015 May;59(5):853-64. doi: 10.1002/mnfr.201400819. Epub 2015 Mar 18.

Abstract

Scope: Acute kidney injury (AKI) is the most frequent and serious complication in sepsis, a potentially deadly inflammatory response induced by bacterial, viral, or fungal infection. LPS-induced AKI is associated with an abnormal inflammatory response, including renal endothelial dysfunction and renal inflammation. Resveratrol, a natural phytoalexin with low toxicity and anti-inflammatory properties, is known to protect endothelial cells and modulate the immune response in sepsis.

Methods and results: This study investigates the potential protective effects of resveratrol on AKI induced by LPS exposure of mice. Resveratrol was administered as a pre- and posttreatment, or as a posttreatment alone following LPS injection and compared to control groups. Resveratrol significantly improved kidney function and lowered serum and kidney tissue inflammatory cytokine levels. Consistently, resveratrol prevented endotoxin-induced disruption of endothelial cell permeability and inhibited inflammation of kidney tissue. Resveratrol treatment attenuated the effects of LPS on macrophages, with significant inhibition of activation, cytokine release, and Toll-like receptor 4 activation. Resveratrol treatment also resulted in decreased expression of iNOS, Bcl-2, and Bcl-xL in macrophages, which was linked with induction of apoptosis in macrophages.

Conclusion: Our studies suggest that resveratrol might represent a novel therapeutic agent to prevent and treat sepsis-induced AKI.

Keywords: AKI; Kidney injury; LPS; Macrophage; Resveratrol.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Acute Kidney Injury / drug therapy*
  • Animals
  • Apoptosis / drug effects
  • Capillary Permeability / drug effects
  • Female
  • Inflammation / prevention & control*
  • Kidney / drug effects
  • Kidney / pathology
  • Kidney / physiology
  • Lipopolysaccharides / toxicity
  • Macrophages / drug effects*
  • Macrophages / immunology
  • Mice
  • Mice, Inbred C57BL
  • NF-kappa B / physiology
  • Resveratrol
  • Signal Transduction / drug effects
  • Stilbenes / pharmacology*
  • Toll-Like Receptor 4 / physiology
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Lipopolysaccharides
  • NF-kappa B
  • Stilbenes
  • Tlr4 protein, mouse
  • Toll-Like Receptor 4
  • Tumor Necrosis Factor-alpha
  • Resveratrol