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

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-α plays a central role in I/R injury and, therefore, down-regulation of TNF-α 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-α 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-α mRNA expression after I/R of the liver was determined by RT-PCR. In untreated rats, TNF-α 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-α 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-α expression.

[1]  G. Wanner,et al.  SIGNIFICANCE OF PROCALCITONIN (PCT) PLASMA LEVELS DURING THE CLINICAL COURSE OF SEVERELY INJURED PATIENTS , 1999 .

[2]  K. Messmer,et al.  Differential effect of anti-TNF-alpha antibody on proinflammatory cytokine release by Kupffer cells following liver ischemia and reperfusion. , 1999, Shock.

[3]  F. Schade,et al.  Peritoneal macrophages from endotoxin-tolerant mice produce an inhibitor of tumor necrosis factor α synthesis and protect against endotoxin shock , 1997 .

[4]  M. Gerritsen,et al.  Cytokine-induced VCAM-1 and ICAM-1 expression in different organs of the mouse. , 1997, Journal of immunology.

[5]  F. Schade,et al.  Endotoxin-tolerant mice produce an inhibitor of tumor necrosis factor synthesis , 1996 .

[6]  T. Mak,et al.  Crucial role of 55-kilodalton TNF receptor in TNF-induced adhesion molecule expression and leukocyte organ infiltration. , 1996, Journal of immunology.

[7]  M. Leist,et al.  The 55-kD Tumor Necrosis Factor Receptor and CD95 Independently Signal Murine Hepatocyte Apoptosis and Subsequent Liver Failure , 1996, Molecular medicine.

[8]  K. Rajewsky,et al.  Interleukin-10 is a central regulator of the response to LPS in murine models of endotoxic shock and the Shwartzman reaction but not endotoxin tolerance. , 1995, The Journal of clinical investigation.

[9]  R. Green,et al.  Tumor necrosis factor–alpha decreases hepatocyte bile salt uptake and mediates endotoxin‐induced cholestasis , 1995, Hepatology.

[10]  S. Arii,et al.  Liver transplantation and hepatic sinusoidal cells , 1995, Journal of gastroenterology and hepatology.

[11]  H. Jaeschke,et al.  Cytokine‐induced upregulation of hepatic intercellular adhesion molecule‐1 messenger RNA expression and its role in the pathophysiology of murine endotoxin shock and acute liver failure , 1995, Hepatology.

[12]  C. Meisel,et al.  Mechanism of endotoxin desensitization: involvement of interleukin 10 and transforming growth factor beta , 1995, The Journal of experimental medicine.

[13]  B. Zingarelli,et al.  INCREASED NITRIC OXIDE SYNTHESIS DURING THE DEVELOPMENT OF ENDOTOXIN TOLERANCE , 1995, Shock.

[14]  M. Leist,et al.  Activation of the 55 kDa TNF receptor is necessary and sufficient for TNF-induced liver failure, hepatocyte apoptosis, and nitrite release. , 1995, Journal of immunology.

[15]  川野克則 Evidence that FK506 Alleviates Ischemia/Reperfusion Injury to the Rat Liver: In vivo Demonstration for Suppression of TNF-α Production in Response to Endotoxemia(FR506によるラット肝における虚血・再灌流障害の軽減: エンドトキシン血症に伴うTNF-α産生抑制のin vivoでの証明) , 1995 .

[16]  F. Schade,et al.  Formation of a TNF synthesis inhibitor in endotoxin tolerance. , 1995, Progress in clinical and biological research.

[17]  D. Remick,et al.  Hepatic ischemia/reperfusion injury: importance of oxidant/tumor necrosis factor interactions. , 1994, The American journal of physiology.

[18]  T. Nakamura,et al.  Pathogenic role of Kupffer cell activation in the reperfusion injury of cold-preserved liver. , 1994, Transplantation.

[19]  D. Remick,et al.  LPS pretreatment protects from hepatic ischemia/reperfusion. , 1994, The Journal of surgical research.

[20]  J. Haas,et al.  Tolerance to lipopolysaccharide involves mobilization of nuclear factor kappa B with predominance of p50 homodimers. , 1994, The Journal of biological chemistry.

[21]  T. Kirikae,et al.  Bacterial endotoxin: molecular relationships of structure to activity and function , 1994, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[22]  K. Messmer,et al.  Role of leukocytes in the initial hepatic microvascular response to endotoxemia. , 1993, Zentralblatt fur Chirurgie.

[23]  P. Vassalli,et al.  The pathophysiology of tumor necrosis factors. , 1992, Annual review of immunology.

[24]  P. Heinrich,et al.  Time course of IL-6 and TNFα release during endotoxin-induced endotoxin tolerance in rats , 1991 .

[25]  P. Heinrich,et al.  Time course of IL-6 and TNF alpha release during endotoxin-induced endotoxin tolerance in rats. , 1991, Biochemical pharmacology.

[26]  R. Strieter,et al.  Role of tumor necrosis factor-alpha in the pathophysiologic alterations after hepatic ischemia/reperfusion injury in the rat. , 1990, The Journal of clinical investigation.

[27]  K. Glaser,et al.  Adaptation to bacterial lipopolysaccharide controls lipopolysaccharide-induced tumor necrosis factor production in rabbit macrophages. , 1990, The Journal of clinical investigation.

[28]  A. Harken,et al.  Endotoxin pretreatment increases endogenous myocardial catalase activity and decreases ischemia-reperfusion injury of isolated rat hearts. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[29]  W. Meyers,et al.  Bile flow--an index of ischemic injury. , 1987, The Journal of surgical research.

[30]  B. Beutler,et al.  Purification of cachectin, a lipoprotein lipase-suppressing hormone secreted by endotoxin-induced RAW 264.7 cells , 1985, The Journal of experimental medicine.

[31]  W. Frederiks,et al.  A model for provoking ischemic necrosis in rat liver parenchyma and its quantitative analysis. , 1982, Experimental pathology.