Characterization of release of tumor necrosis factor, interleukin-1, and superoxide anion from equine white blood cells in response to endotoxin.
Abstract: Direct effects of endotoxin (lipopolysaccharide [LPS]) on equine WBC are known to stimulate the release of a variety of mediators including thromboxane, prostacyclin, and leukotrienes. In this study, 0.1 microgram of LPS/ml stimulated an early increase in tumor necrosis factor, succeeded by an increase in interleukin-1, but concentrations of LPS up to 5.0 micrograms/ml caused no significant increase in superoxide anion release. The concentration of LPS (0.1 microgram/ml) used in this experiment was in the range of concentrations measured in plasma of some horses with gastrointestinal problems. These results indicate that mediators released in response to low concentrations of LPS may be responsible for many of the LPS-induced pathophysiologic effects. This is indicated because concentrations of LPS detected in plasma of some horses with severe gastrointestinal problems are approximately 0.1 microgram/ml, a concentration that will stimulate cells to produce tumor necrosis factor, but will not stimulate any other measurable cytotoxic effect.
Publication Date: 1990-08-01 PubMed ID: 2167032
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- Journal Article
Summary
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The research article aims to understand the impact of endotoxins on equine white blood cells (WBC), indicating that low concentrations of such toxins trigger the release of tumor necrosis factor and interleukin-1 but does not necessarily increase the release of superoxide anion.
Background
- Endotoxins, specifically lipopolysaccharide (LPS), are recognized for their stimulant effects on equine white blood cells. Upon stimulation, these cells release various mediators such as thromboxane, prostacyclin, and leukotrienes.
- The research primarily focuses on the release of tumor necrosis factor, interleukin-1, and superoxide anion in response to LPS.
Research Methodology
- The concentration of LPS used in the experiment was 0.1 microgram/ml. This concentration triggered an initial increase in the production of tumor necrosing factors, followed by an increase in interleukin-1.
- However, even when the LPS concentration was increased to 5.0 micrograms/ml, there was no significant change in the release of superoxide anion.
Research Findings and Conclusion
- The selected LPS concentration used in the research aligns with the levels typically found in the plasma of horses suffering from gastrointestinal issues.
- The outcomes suggest that the mediators released in reaction to small quantities of LPS may lead to many of its pathophysiological effects.
- The findings are indicative, especially since the levels of LPS detected in the plasma of some horses with severe gastrointestinal problems can stimulate cells to produce tumor necrosis factor without triggering any other measurable cytotoxic effect.
Cite This Article
APA
Seethanathan P, Bottoms GD, Schafer K.
(1990).
Characterization of release of tumor necrosis factor, interleukin-1, and superoxide anion from equine white blood cells in response to endotoxin.
Am J Vet Res, 51(8), 1221-1225.
Publication
Researcher Affiliations
- Department of Veterinary Physiology and Pharmacology, School of Veterinary Medicine, Purdue University, West Lafayette, IN 47907.
MeSH Terms
- Animals
- Cell Line
- Female
- Horses / blood
- Interleukin-1 / blood
- Leukocytes / drug effects
- Leukocytes / metabolism
- Lipopolysaccharides / pharmacology
- Male
- Superoxides / blood
- Time Factors
- Tumor Necrosis Factor-alpha / metabolism
Citations
This article has been cited 2 times.- Grulke S, Benbarek H, Caudron I, Deby-Dupont G, Mathy-Hartert M, Farnir F, Deby C, Lamy M, Serteyn D. Plasma myeloperoxidase level and polymorphonuclear leukocyte activation in horses suffering from large intestinal obstruction requiring surgery: preliminary results. Can J Vet Res 1999 Apr;63(2):142-7.
- Benbarek H, Deby-Dupont G, Caudron I, Deby C, Lamy M, Serteyn D. Failure of lipopolysaccharides to directly trigger the chemiluminescence response of isolated equine polymorphonuclear leukocytes. Vet Res Commun 1997 Oct;21(7):477-82.
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