HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Coagulation blockade prevents sepsis-induced respiratory and renal failure in baboons.

Abstract
Sepsis-induced tissue factor (TF) expression activates coagulation in the lung and leads to a procoagulant environment, which results in fibrin deposition and potentiates inflammation. We hypothesized that preventing initiation of coagulation at TF-Factor VIIa (FVIIa) complex would block fibrin deposition and control inflammation in sepsis, thereby limiting acute lung injury (ALI) and other organ damage in baboons. A model of ALI was used in which adult baboons were primed with killed Escherichia coli (1 x 10(9) CFU/kg), and bacteremic sepsis was induced 12 h later by infusion of live E. coli at 1 x 10(10) CFU/kg. Animals in the treatment group were given a competitive inhibitor of TF, site-inactivated FVIIa (FVIIai), intravenously at the time of the infusion of live bacteria and monitored physiologically for another 36 h. FVIIai dramatically protected gas exchange and lung compliance, prevented lung edema and pulmonary hypertension, and preserved renal function relative to vehicle (all p < 0.05). Treatment attenuated sepsis-induced fibrinogen depletion (p < 0.01) and decreased systemic proinflammatory cytokine responses, for example, interleukin 6 (p < 0.01). The protective effects of TF blockade in sepsis-induced ALI were confirmed by using tissue factor pathway inhibitor. The results show that TF-FVIIa complex contributes to organ injury in septic primates in part through selective stimulation of proinflammatory cytokine release and fibrin deposition.
AuthorsK E Welty-Wolf, M S Carraway, D L Miller, T L Ortel, M Ezban, A J Ghio, S Idell, C A Piantadosi
JournalAmerican journal of respiratory and critical care medicine (Am J Respir Crit Care Med) Vol. 164 Issue 10 Pt 1 Pg. 1988-96 (Nov 15 2001) ISSN: 1073-449X [Print] United States
PMID11734456 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Interleukin-6
  • Tumor Necrosis Factor-alpha
  • Factor VIIIa
  • Fibrinogen
  • Thromboplastin
Topics
  • Acute Kidney Injury (microbiology, prevention & control)
  • Animals
  • Bacteremia (blood, complications, immunology, pathology, physiopathology)
  • Blood Coagulation (drug effects, physiology)
  • Disease Models, Animal
  • Drug Evaluation, Preclinical
  • Escherichia coli Infections (blood, complications, immunology, physiopathology)
  • Factor VIIIa (physiology, therapeutic use)
  • Fibrinogen (analysis, drug effects)
  • Hemodynamics (drug effects)
  • Inflammation
  • Interleukin-6 (blood)
  • Kidney Function Tests
  • Lung Compliance (drug effects)
  • Male
  • Papio
  • Pulmonary Edema (microbiology, prevention & control)
  • Pulmonary Gas Exchange (drug effects)
  • Random Allocation
  • Respiratory Distress Syndrome (microbiology, prevention & control)
  • Thromboplastin (antagonists & inhibitors, physiology)
  • Tumor Necrosis Factor-alpha (metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: