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Equine veterinary journal1994; 26(6); 474-481; doi: 10.1111/j.2042-3306.1994.tb04053.x

Regulation of equine fibrinolysis in blood and peritoneal fluid based on a study of colic cases and induced endotoxaemia.

Abstract: Much of the pathophysiology associated with equine gastrointestinal diseases is attributed to the effects of endotoxin on haemostasis. Because little is known about the responses of the equine fibrinolytic system to endotoxin, regulation of the system was investigated. Tissue-type plasminogen activator (t-PA) and plasminogen activator inhibitor type-1 (PAI-1) were identified as the primary plasminogen activator and plasminogen activator inhibitor, respectively, in equine blood. Under experimental conditions, the equine fibrinolytic system responded to endotoxin in a manner similar to that reported in man, with an early, transient increase in t-PA activity followed by an overwhelming and prolonged increase in activity of PAI-1. To investigate the response of the equine fibrinolytic system to clinical endotoxaemia, endotoxin concentrations were measured in plasma and peritoneal fluid, and activities of t-PA and PAI-1 were compared between healthy horses (n = 38) and horses with naturally occurring gastrointestinal diseases (n = 150). It was observed that plasma PAI-1 and peritoneal t-PA were increased concurrently in abnormal horses; and that these increases were associated with the presence of endotoxin. The results of this study suggest that 1) fibrinolysis is regulated in horses in a manner similar to that in man; 2) regulation of fibrinolysis is altered in endotoxaemic horses with gastrointestinal diseases; 3) events occurring in the vascular system may not reflect those in the peritoneal cavity; and 4) t-PA activity is increased in the peritoneal fluid of endotoxaemic horses with gastrointestinal diseases.
Publication Date: 1994-11-01 PubMed ID: 7889922DOI: 10.1111/j.2042-3306.1994.tb04053.xGoogle Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research on equine gastrointestinal diseases highlights that much of the illness is due to the impact of endotoxin on haemostasis. In this study, the main fibrinogen activator and inhibitor, t-PA and PAI-1 respectively, were identified in horse blood. Through experiments, it was noted that the equine fibrinolytic system reacts to endotoxin similarly to humans, with an early rise in t-PA followed by a larger and longer increase in PAI-1 activity. Comparing healthy and diseased horses, the study found that plasma PAI-1 and peritoneal t-PA levels were higher in the diseased horses and correlated with the presence of endotoxin. The study suggests that fibrinolysis regulation is the same in horses and humans and that it is altered in sick horses with gastrointestinal diseases.

Research Objective and Methodology

  • Scientists aimed to comprehend how the equine fibrinolytic system responds to endotoxin, as this was previously less understood. They sought to explore this by identifying and studying the key elements, t-PA and PAI-1, present in equine blood.
  • Researchers designed experiments that exposed the equine fibrinolytic system to endotoxin. The response of the fibrinolytic system was then observed and compared with the reported response in humans.
  • This research also featured an analysis of plasma and peritoneal fluid of healthy horses (n=38) and horses suffering from gastrointestinal diseases (n=150) to study the response ofthis system in clinical endotoxaemia (when there are endotoxins present in the blood).

Findings and Conclusion

  • Researchers observed that plasma PAI-1 and peritoneal t-PA were increased simultaneously in horses with gastrointestinal diseases; these increases were associated with endotoxin presence.
  • The study established that fibrinolysis in horses operates similarly to that in humans — characterized by an initial t-PA activity rise followed by a sustained PAI-1 activity increase when exposed to endotoxins.
  • The research also identified that the regulation of fibrinolysis changes in horses afflicted with gastrointestinal diseases, implying a specific response to endotoxaemia, suggesting a link between endotoxaemia and the progression of gastrointestinal diseases in horses.
  • The study concluded that events in the vascular system may not always reflect the events in the peritoneal cavity (part of the abdomen), indicating the complexity of the equine fibrinolytic response and underscoring the significance of localized analyses in understanding the full impact of endotoxins.

Cite This Article

APA
Collatos C, Barton MH, Schleef R, Prasse KW, Moore JN. (1994). Regulation of equine fibrinolysis in blood and peritoneal fluid based on a study of colic cases and induced endotoxaemia. Equine Vet J, 26(6), 474-481. https://doi.org/10.1111/j.2042-3306.1994.tb04053.x

Publication

ISSN: 0425-1644
NlmUniqueID: 0173320
Country: United States
Language: English
Volume: 26
Issue: 6
Pages: 474-481

Researcher Affiliations

Collatos, C
  • Department of Large Animal Medicine, College of Veterinary Medicine, University of Georgia, Athens 30602.
Barton, M H
    Schleef, R
      Prasse, K W
        Moore, J N

          MeSH Terms

          • Animals
          • Ascitic Fluid / blood
          • Ascitic Fluid / veterinary
          • Colic / blood
          • Colic / veterinary
          • Endotoxins
          • Female
          • Fibrinolysis / physiology
          • Horse Diseases / blood
          • Horses / blood
          • Humans
          • Male
          • Plasminogen Activator Inhibitor 1 / metabolism
          • Plasminogen Activators / metabolism
          • Tissue Plasminogen Activator / metabolism
          • Toxemia / blood
          • Toxemia / veterinary

          Citations

          This article has been cited 1 times.
          1. Lillich JD, Ray-Miller W, Silver KS, Davis EG, Schultz BD. Intra-abdominal hyaluronan concentration in peritoneal fluid of horses with sudden signs of severe abdominal pain. Am J Vet Res 2011 Dec;72(12):1666-73.
            doi: 10.2460/ajvr.72.12.1666pubmed: 22126696google scholar: lookup