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American journal of veterinary research2010; 71(10); 1162-1169; doi: 10.2460/ajvr.71.10.1162

Expression of genes associated with inflammation induced by ex vivo exposure to lipopolysaccharide in peripheral blood leukocytes from horses with gastrointestinal disease.

Abstract: To investigate the effect of ex vivo exposure to lipopolysaccharide (LPS) on the expression of inflammatory genes in leukocytes from horses with gastrointestinal (Gl) disease and determine whether the pattern or magnitude of the response to LPS correlated with the type of disease and outcome. Methods: 49 horses with Gl disease and 10 healthy horses Methods: Leukocytes were isolated from blood samples and submitted to 3 protocols: immediate freezing, freezing after 4-hour incubation in medium, and freezing after 4-hour incubation in medium containing LPS. Expression of 14 genes associated with inflammation was assessed via PCR assay. Results were compared by disease type and outcome Results: Horses with Gl disease had colic of unknown etiology (n=8), Gl inflammation or strangulation (18), or nonstrangulating Gl obstruction (23). Among the 44 horses receiving treatment, 38 were discharged from the hospital and 6 died or were euthanized. Incubation of leukocytes in medium alone changed the expression of several genes. Incubation with LPS resulted in increased expression of interleukin-10 and monocyte chemotactic protein-3 in leukocytes from healthy and sick horses. Leukocytes from horses with nonstrangulating obstruction and horses that survived had less pronounced LPS-induced increases in interleukin-10 expression than did cells from healthy horses. The opposite was evident for monocyte chemotactic protein-3. Conclusions: No evidence existed for a reduced response of leukocytes from horses with gastrointestinal disease to ex vivo exposure to LPS. Leukocyte expression of inflammatory genes after ex vivo incubation with LPS appeared to be related to pathogenesis and prognosis.
Publication Date: 2010-10-06 PubMed ID: 20919902DOI: 10.2460/ajvr.71.10.1162Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research article involves a study on how inflammatory genes in white blood cells (leukocytes) from horses with gastrointestinal disease respond to exposure to lipopolysaccharide (LPS). The researchers found that these leukocytes’ gene expression changed according to pathogenesis and prognosis of the disease, and there was no indication of decreased leukocyte response to LPS.

Study Objective and Methods

  • The study’s goal was to see how exposure to LPS—a common component of some types of bacteria—affects the expression of inflammatory genes in leukocytes from horses with gastrointestinal disease. The researchers were also interested in whether the response to LPS differed according to the type of gastrointestinal disease and its outcome.
  • The study involved 49 horses with gastrointestinal disease and 10 healthy horses. From these horses, the researchers isolated leukocytes from blood samples and subjected them to three tests: immediate freezing, freezing after incubating in a medium for 4 hours, and freezing after incubating in a medium with LPS for 4 hours.
  • The expression of 14 different genes associated with inflammation was analyzed using a Polymerase Chain Reaction (PCR) assay. The researchers compared the results according to the type of disease and its outcome.

Study Results

  • The conditions of the horses with gastrointestinal disease varied: 8 had colic of unknown origin, 18 had gastrointestinal inflammation or strangulation, and 23 had non-strangulating gastrointestinal obstruction. Out of the 44 horses that received treatment, 38 were discharged from the hospital, and 6 either died or were euthanized.
  • The researchers observed that incubating the leukocytes in medium alone altered the expression of several genes. When the leukocytes were incubated with LPS, there was an increase in the expression of interleukin-10 and monocyte chemotactic protein-3 in both healthy and sick horses.
  • Leukocytes from horses with non-strangulating obstruction and horses that survived exhibited less pronounced LPS-induced increases in interleukin-10 expression compared to cells from healthy horses. The opposite was observed for monocyte chemotactic protein-3.

Study Conclusions

  • There was no evidence suggesting a diminished response of leukocytes from horses with gastrointestinal disease to ex vivo exposure to LPS. Instead, the pattern of inflammatory gene expression in leukocytes upon incubation with LPS appeared to be linked to the disease’s pathogenesis (origination and development) and prognosis (predicted outcome).

Cite This Article

APA
Lopes MA, Salter CE, Vandenplas ML, Berghaus R, Hurley DJ, Moore JN. (2010). Expression of genes associated with inflammation induced by ex vivo exposure to lipopolysaccharide in peripheral blood leukocytes from horses with gastrointestinal disease. Am J Vet Res, 71(10), 1162-1169. https://doi.org/10.2460/ajvr.71.10.1162

Publication

ISSN: 0002-9645
NlmUniqueID: 0375011
Country: United States
Language: English
Volume: 71
Issue: 10
Pages: 1162-1169

Researcher Affiliations

Lopes, Marco A F
  • Department of Large Animal Medicine, College of Veterinary Medicine, University of Georgia, Athens, GA 30602, USA. maflopes@gmail.com
Salter, Caroline E
    Vandenplas, Michel L
      Berghaus, Roy
        Hurley, David J
          Moore, James N

            MeSH Terms

            • Animals
            • Cells, Cultured
            • Cytokines / genetics
            • Cytokines / metabolism
            • Gastrointestinal Diseases / blood
            • Gastrointestinal Diseases / metabolism
            • Gastrointestinal Diseases / veterinary
            • Gene Expression Regulation / physiology
            • Horse Diseases / blood
            • Horse Diseases / metabolism
            • Horses
            • Inflammation / metabolism
            • Inflammation / veterinary
            • Leukocytes / drug effects
            • Lipopolysaccharides / toxicity

            Citations

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