Postconditioning ameliorates lipid peroxidation in liver ischemia-reperfusion injury in rats

Acta Cir Bras. 2009 Jan-Feb;24(1):52-6. doi: 10.1590/s0102-86502009000100011.

Abstract

Purpose: Liver ischemia-reperfusion injury is a phenomenon presents in events like liver resections and transplantation. The restoration of blood flow may leads to local and systemic injury. Several techniques have been developed in order to avoid or ameliorate ischemia-reperfusion injury in clinical situations. The application of a stutter reperfusion after the ischemic event (postconditioning) could alters the hydrodynamics and stimulates endogenous mechanisms that attenuate the reperfusion injury. The present study was designed to evaluate the potential protective effect of postconditioning in a model of ischemia-reperfusion in rats.

Methods: Hepatic anterior pedicle of median and left anterolateral segments were exposed and clamped for 1 hour. Two hours later, clamp was released in two different ways: Control Group (n=7): clamp was release straightforward; Postconditioning Group (n=7): clamp was released intermittently. Lipid peroxidation (malondialdehyde) and expression of the glutathione-s-transferase-alpha-3 gene were studied.

Results: Lipid peroxidation was significantly decreased in ischemic and non-ischemic liver by postconditioning. GST- alpha3 gene was overexpressed in post-conditioned group, but not significantly.

Conclusion: Postconditioning induced hepatoprotection by reducing lipid peroxidation in the ischemic and non-ischemic liver.

MeSH terms

  • Animals
  • Biomarkers / blood
  • Glutathione Transferase / blood
  • Glutathione Transferase / genetics
  • Ischemia / prevention & control*
  • Ischemic Preconditioning*
  • Isoenzymes / blood
  • Isoenzymes / genetics
  • Lipid Peroxidation / physiology*
  • Liver / blood supply*
  • Male
  • Malondialdehyde / blood
  • Random Allocation
  • Rats
  • Rats, Wistar
  • Reperfusion Injury / metabolism
  • Reperfusion Injury / prevention & control*

Substances

  • Biomarkers
  • Isoenzymes
  • Malondialdehyde
  • Glutathione Transferase
  • glutathione S-transferase alpha