Endotoxin tolerance protects against local hepatic ischemia/reperfusion injury in the rat

J Endotoxin Res. 2000;6(4):321-8. doi: 10.1179/096805100101532216.

Abstract

Liver surgery and liver transplantation as well as circulatory shock are often associated with hepatic ischemia/reperfusion (I/R) injury. Recent evidence suggests that TNF-alpha plays a central role in I/R injury and, therefore, down-regulation of TNF-alpha seems to be a promising way to protect against the deleterious consequences of I/R. Endotoxin tolerance represents a state of unresponsiveness to endotoxin and is associated with diminished TNF-alpha production. Thus, the effect of endotoxin tolerance on hepatic I/R injury of the liver was investigated in a rat model. I/R injury was induced by temporary ischemia of the left lateral liver lobe for 90 min followed by a 3 h observation period of reperfusion. I/R injury resulted in functional hepatic disorder characterized by a decrease both in bile flow and bile acid concentration and 50% mortality. This was prevented by induction of endotoxin tolerance. Hepatic TNF-alpha mRNA expression after I/R of the liver was determined by RT-PCR. In untreated rats, TNF-alpha mRNA was induced in the liver 60 min after reperfusion and further increased until 3 h after reperfusion. In contrast, in endotoxin-tolerant rats, no increases in TNF-alpha mRNA expression were detected. This suggests that induction of endotoxin tolerance protects against hepatic I/R injury possibly via down-regulation of intra-organ TNF-alpha expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Bile / physiology
  • Bile Acids and Salts / metabolism
  • DNA Primers / genetics
  • Down-Regulation / drug effects
  • Drug Tolerance
  • Endotoxins / toxicity*
  • Liver / drug effects*
  • Liver / injuries*
  • Liver / physiopathology
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Reperfusion Injury / etiology
  • Reperfusion Injury / genetics
  • Reperfusion Injury / physiopathology
  • Reperfusion Injury / prevention & control*
  • Tumor Necrosis Factor-alpha / genetics

Substances

  • Bile Acids and Salts
  • DNA Primers
  • Endotoxins
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha