Inactivation of the small GTPase Rac1 protects the liver from ischemia/reperfusion injury in the rat

Surgery. 2003 Sep;134(3):480-91. doi: 10.1067/s0039-6060(03)00256-3.

Abstract

Background: In ischemia/reperfusion (I/R) injury, a massive generation of reactive oxygen species (ROS) after reperfusion is a critical factor. Rac, a member of the Rho GTPase superfamily, plays important roles in the production of ROS and activation of nuclear factor-kappaB (NF-kappaB) in vitro. However, the exact role of Rac in the ROS production and NF-kappaB activation in vivo after I/R is still obscure.

Methods: We blocked Rac1 activity in the rat liver using adenovirus encoding a dominant negative rac1 mutant (Ad5N17Rac1) and examined whether inactivation of Rac1 could prevent ROS generation in the hepatic I/R injury. Seventy-two hours after the adenoviral infection, hepatic I/R was induced by Pringle's maneuver for 20 minutes, followed by reperfusion in the rats.

Results: Ad5N17Rac1 infection significantly attenuated ROS production after reperfusion and suppressed the hepatic injury. Furthermore, N17Rac1 suppressed NF-kappaB activation and messenger RNA expression of tumor necrosis factor-alpha (TNF-alpha) and inducible nitric oxide synthetase (iNOS). Ad5LacZ, a control adenovirus, had no effect on the induced hepatic I/R injury, nor did it affect NF-kappaB activation. Immunohistochemical analysis of NF-kappaB (p65) revealed that translocation of p65 to the nucleus after reperfusion was blocked in many of non-parenchymal cells (NPCs) and in hepatocytes in the Ad5N17Rac1-infected liver.

Conclusion: We conclude that Rac1 is required in ROS generation and NF-kappaB activation after hepatic I/R in vivo, and that inactivation of NF-kappaB in NPCs and suppression of ROS generation in NPCs and hepatocytes possibly account for the protective effect of N17Rac1 in this study.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Active Transport, Cell Nucleus
  • Adenoviridae / genetics
  • Animals
  • DNA / metabolism
  • Gene Transfer, Horizontal
  • Liver / blood supply*
  • Male
  • Mutation
  • NF-kappa B / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Reactive Oxygen Species
  • Reperfusion Injury / prevention & control*
  • rac1 GTP-Binding Protein / genetics
  • rac1 GTP-Binding Protein / physiology*

Substances

  • NF-kappa B
  • Reactive Oxygen Species
  • DNA
  • rac1 GTP-Binding Protein