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Journal of veterinary pharmacology and therapeutics1996; 19(1); 44-49; doi: 10.1111/j.1365-2885.1996.tb00007.x

Characterization of a sterile soft-tissue inflammation model in thoroughbred horses.

Abstract: This paper describes the use of subcutaneously-placed tissue chambers as a sterile soft-tissue inflammation model in Thoroughbred horses. Acute, non-immune inflammation was initiated by injecting a sterile lambda carrageenan solution into a tissue chamber. This model was used to study the temporal changes in oxygen and carbon dioxide tensions, pH, bicarbonate, protein, albumin, prostaglandin E2 (PGE2) and leukotriene B4 (LTB4) concentrations, cell counts and differential counts in tissue fluid from inflamed tissue chambers and control chambers. Skin temperatures over control and inflamed chambers were also compared. Carrageenan-induced inflammation resulted in significant increases in tissue-fluid carbon dioxide tension, leucocyte count, albumin, and PGE2 and LTB4 concentrations. It also resulted in a significant decrease in tissue fluid pH and HCO3-concentration. Inflammation did not result in significant changes in tissue-fluid protein concentration, differential cell counts or skin temperature over the chambers. The use of this type of tissue chamber is well-suited for studying the pathophysiology of a self-contained, non-immune inflammatory process. The model described in this paper could prove to be very useful in studies of the distribution of anti-inflammatory drugs and the effects of such drugs on various aspects of the inflammatory process.
Publication Date: 1996-02-01 PubMed ID: 8992025DOI: 10.1111/j.1365-2885.1996.tb00007.xGoogle Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research paper discusses a new method for eliciting sterile soft-tissue inflammation in Thoroughbred horses via subcutaneous tissue chambers injecting with sterile lambda carrageenan solution, and the subsequent effects of this inflammation on various measures of tissue fluid and temperature.

Model and Procedure

  • The researchers conducted this study by using tissue chambers, placed under the skin of the horse. The purpose of these chambers was to create a controlled, isolate area where inflammation could be induced and monitored.
  • Inflammation was initiated by injecting a sterile solution of lambda carrageenan into these tissue chambers. Lambda carrageenan is a substance extracted from red seaweed which is known to create inflammation responses in the body.

Measurements and Results

  • Over the course of the experiment, the researchers observed and recorded multiple changes in the inflamed tissue chambers and control (non-inflamed) chambers. They monitored temporal changes in certain aspect of the tissue fluid including oxygen and carbon dioxide tensions, pH, bicarbonate, protein, albumin, prostaglandin E2 (PGE2) and leukotriene B4 (LTB4) concentrations, and cell counts, in particular leucocytes which are key for immune response.
  • Furthermore, skin temperatures over the inflamed and control chambers were compared to see if the inflammation caused any noticeable difference.
  • The results showed that the carrageenan-induced inflammation resulted in significant increases in tissue-fluid carbon dioxide tension, leucocyte count, albumin, and PGE2 and LTB4 concentrations, which are biomarkers associated with inflammation in the body.
  • Interestingly, they also found that the inflammation caused a significant decrease in tissue fluid’s pH and bicarbonate concentration, suggesting an accumulation of acids due to inflammation.
  • However, no significant changes were noted in tissue-fluid protein concentration, differential cell counts, or skin temperature over the chambers after inflammation was induced.

Conclusions and Implications

  • The authors concluded that this subcutaneous tissue chamber model could be an effective method for studying the pathophysiology of self-contained, non-immune inflammatory processes.
  • The researchers suggest the model could also be very useful in studying the distribution and effects of anti-inflammatory drugs on various aspects of the inflammatory process, which opens up avenues for new research into the treatment of inflammation in racehorses and other equine species.

Cite This Article

APA
Guthrie AJ, Short CR, Swan GE, Mülders MS, Killeen VM, Nurton JP. (1996). Characterization of a sterile soft-tissue inflammation model in thoroughbred horses. J Vet Pharmacol Ther, 19(1), 44-49. https://doi.org/10.1111/j.1365-2885.1996.tb00007.x

Publication

ISSN: 0140-7783
NlmUniqueID: 7910920
Country: England
Language: English
Volume: 19
Issue: 1
Pages: 44-49

Researcher Affiliations

Guthrie, A J
  • Equine Research Centre, Faculty of Veterinary Science, University of Pretoria, Onderstepoort, South Africa.
Short, C R
    Swan, G E
      Mülders, M S
        Killeen, V M
          Nurton, J P

            MeSH Terms

            • Animals
            • Bicarbonates / metabolism
            • Carbon Dioxide / metabolism
            • Diffusion Chambers, Culture / veterinary
            • Dinoprostone / metabolism
            • Disease Models, Animal
            • Enzyme-Linked Immunosorbent Assay / veterinary
            • Exudates and Transudates / chemistry
            • Exudates and Transudates / cytology
            • Female
            • Horse Diseases / physiopathology
            • Horses
            • Hydrogen-Ion Concentration
            • Inflammation / physiopathology
            • Inflammation / veterinary
            • Leukocyte Count / veterinary
            • Leukotriene B4 / metabolism
            • Oxygen Consumption / physiology
            • Proteins / metabolism
            • Skin Temperature
            • Soft Tissue Infections / physiopathology
            • Soft Tissue Infections / veterinary
            • Software

            Citations

            This article has been cited 1 times.
            1. Radhakrishnan R, Moore SA, Sluka KA. Unilateral carrageenan injection into muscle or joint induces chronic bilateral hyperalgesia in rats.. Pain 2003 Aug;104(3):567-577.
              doi: 10.1016/S0304-3959(03)00114-3pubmed: 12927629google scholar: lookup