TRAUMA-HEMORRHAGIC SHOCK MESENTERIC LYMPH FROM RAT CONTAINS A MODIFIED FORM OF ALBUMIN THAT IS IMPLICATED IN ENDOTHELIAL CELL TOXICITY

It has been proposed that factors originating from the gut after severe trauma/shock are introduced into the systemic circulation through the mesenteric lymphatics and are responsible for the cellular injury and inflammation that culminates in acute multiple organ dysfunction syndrome (MODS). Indeed, it has been shown that lymph collected from shocked but not sham-shocked animals causes endothelial cell death, neutrophil activation, and bone marrow (BM) colony growth suppression in vitro. In an attempt to isolate the factor(s) in lymph responsible for endothelial cell toxicity, lymph from shock and sham animals was fractionated by solid phase extraction (SPE) and ion exchange chromatography (IEX). The separation of shock lymph by both methodologies yielded two fractions having major detectable toxicity to endothelial cells, whereas no toxicity was detected from sham lymph separations by either method. Subsequent analysis of each SPE toxic fraction by gel electrophoresis and mass spectrometry suggests the toxicity is associated with a modified form of rat serum albumin (mod-RSA) and multiple lipid-based factors. Therefore, we have been able to demonstrate by two different separation techniques that shock lymph contains two or more factors that may account for the toxicity to endothelial cells. Further investigations are needed to determine the type of RSA modification and the identity of the lipid factors and their role in MODS.

[1]  E. Deitch,et al.  Hemorrhagic shock induces endothelial cell apoptosis, which is mediated by factors contained in mesenteric lymph , 2004, Critical care medicine.

[2]  L. Magnotti,et al.  Pancreatic Duct Ligation Reduces Lung Injury Following Trauma and Hemorrhagic Shock , 2004, Annals of surgery.

[3]  R. Forsythe,et al.  THE ROLE OF LYMPH FACTORS IN LUNG INJURY, BONE MARROW SUPPRESSION, AND ENDOTHELIAL CELL DYSFUNCTION IN A PRIMATE MODEL OF TRAUMA-HEMORRHAGIC SHOCK , 2004, Shock.

[4]  E. Deitch,et al.  Albumin Protects Against Gut-Induced Lung Injury In Vitro and In Vivo , 2004, Annals of surgery.

[5]  E. Deitch,et al.  A study of the biologic activity of trauma-hemorrhagic shock mesenteric lymph over time and the relative role of cytokines. , 2004, Surgery.

[6]  E. Deitch,et al.  Trauma-hemorrhagic shock-induced up-regulation of endothelial cell adhesion molecules is blunted by mesenteric lymph duct ligation , 2004, Critical care medicine.

[7]  D. Dries Sepsis and Multiple Organ Dysfunction: A Multidisciplinary Approach , 2004 .

[8]  G. Schmid-Schönbein,et al.  Characterization of Two Classes of Pancreatic Shock Factors: Functional Differences Exhibited by Hydrophilic and Hydrophobic Shock Factors , 2003, Shock.

[9]  E. Deitch,et al.  Factors in intestinal lymph after shock increase neutrophil adhesion molecule expression and pulmonary leukosequestration. , 2003, The Journal of trauma.

[10]  E. Deitch,et al.  Serine Proteases Are Involved in the Pathogenesis of Trauma-Hemorrhagic Shock-Induced Gut and Lung Injury , 2003, Shock.

[11]  E. Deitch,et al.  Trauma/Hemorrhagic Shock Mesenteric Lymph Upregulates Adhesion Molecule Expression and IL-6 Production in Human Umbilical Vein Endothelial Cells , 2002, Shock.

[12]  G. Schmid-Schönbein,et al.  Protease Inhibition in the Intestinal Lumen: Attenuation of Systemic Inflammation and Early Indicators of Multiple Organ Failure in Shock , 2002, Shock.

[13]  John M. Adams,et al.  Entry of gut lymph into the circulation primes rat neutrophil respiratory burst in hemorrhagic shock , 2001, Critical care medicine.

[14]  E. Deitch,et al.  Mesenteric lymph from rats subjected to trauma-hemorrhagic shock are injurious to rat pulmonary microvascular endothelial cells as well as human umbilical vein endothelial cells. , 2001, Shock.

[15]  R. Forsythe,et al.  Hematopoietic failure after hemorrhagic shock is mediated partially through mesenteric lymph , 2001, Critical care medicine.

[16]  W. Hörl,et al.  Serum Proteins Modified by Neutrophil-Derived Oxidants as Mediators of Neutrophil Stimulation1 , 2001, The Journal of Immunology.

[17]  E. Deitch Role of the gut lymphatic system in multiple organ failure , 2001, Current opinion in critical care.

[18]  E. Deitch,et al.  Factors larger than 100 kd in post-hemorrhagic shock mesenteric lymph are toxic for endothelial cells. , 2001, Surgery.

[19]  D. Bar-Or,et al.  A novel assay for cobalt-albumin binding and its potential as a marker for myocardial ischemia-a preliminary report. , 2000, The Journal of emergency medicine.

[20]  E. Moore,et al.  The lipid fraction of post-hemorrhagic shock mesenteric lymph (PHSML) inhibits neutrophil apoptosis and enhances cytotoxic potential. , 2000, Shock.

[21]  G. Schmid-Schönbein,et al.  The Pancreas as a Source of Cardiovascular Cell Activating Factors , 2000, Microcirculation.

[22]  D. Herndon,et al.  Gut epithelial apoptosis after severe burn: effects of gut hypoperfusion. , 2000, Journal of the American College of Surgeons.

[23]  E. Kistler,et al.  Generation of in vivo activating factors in the ischemic intestine by pancreatic enzymes. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[24]  E. Moore,et al.  Posthemorrhagic shock mesenteric lymph primes circulating neutrophils and provokes lung injury. , 1999, The Journal of surgical research.

[25]  L. Magnotti,et al.  Gut-derived mesenteric lymph but not portal blood increases endothelial cell permeability and promotes lung injury after hemorrhagic shock. , 1998, Annals of surgery.

[26]  P. Faries,et al.  Intestinal permeability correlates with severity of injury in trauma patients. , 1998, The Journal of trauma.

[27]  G. Jerums,et al.  Vascular hypertrophy in experimental diabetes. Role of advanced glycation end products. , 1997, The Journal of clinical investigation.

[28]  E. Moore,et al.  Splanchnic ischaemia/reperfusion and multiple organ failure. , 1996, British journal of anaesthesia.

[29]  K. Kudsk,et al.  Increased intestinal permeability following blunt and penetrating trauma. , 1995, Critical care medicine.

[30]  C. Ryan,et al.  Increased gut permeability early after burns correlates with the extent of burn injury , 1992, Critical care medicine.

[31]  E. Deitch,et al.  Multiple organ failure. Pathophysiology and potential future therapy. , 1992, Annals of surgery.

[32]  J. Vane,et al.  Regulatory functions of the vascular endothelium. , 1990, The New England journal of medicine.

[33]  E. Deitch Intestinal permeability is increased in burn patients shortly after injury , 1990, Surgery.

[34]  R. Berg,et al.  Hemorrhagic shock-induced bacterial translocation is reduced by xanthine oxidase inhibition or inactivation. , 1988, Surgery.

[35]  J. Ramachandran,et al.  Regulation of actin in rat adrenocortical cells by corticotropin. , 1981, The Journal of biological chemistry.

[36]  J. Baynes,et al.  Nonenzymatic glucosylation of rat albumin. Studies in vitro and in vivo. , 1979, The Journal of biological chemistry.

[37]  E. Deitch,et al.  Mesenteric lymph duct ligation prevents shock-induced RBC deformability and shape changes. , 2003, The Journal of surgical research.

[38]  T. Peters The Biosynthesis of Rat Serum Albumin , 2001 .