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Journal of veterinary pharmacology and therapeutics1984; 7(1); 65-72; doi: 10.1111/j.1365-2885.1984.tb00881.x

Arachidonic acid metabolites in carrageenin-induced equine inflammatory exudate.

Abstract: The presence of cyclooxygenase products of arachidonic acid metabolism in carrageenin-induced inflammatory exudate was investigated in ponies using two models. In the first model, an inflammatory response was stimulated by injecting carrageenin into subcutaneously implanted polypropylene tissue cages and exudates were collected at five predetermined times between 3 and 48 h. In the second model, exudates were harvested at 6, 12 and 24 h from carrageenin-impregnated polyester sponges which had also been inserted beneath the skin. Prostaglandin (PG) E2, thromboxane (TX) B2 and the stable breakdown-product of prostacyclin (PGI2), 6-keto-PGF1 alpha, in exudates were measured by radio-immunoassay (RIA); PGE2-like and PGF2 alpha-like activities were bioassayed following an acid-lipid extraction technique which provided a recovery rate of 78%. Agreement between RIA and bioassay was within acceptable limits. In Model 1, using RIA, mean PGE2 concentration reached 197 ng X ml-1 at 12 h decreasing to less than 12 ng X ml-1 at 24 h. Mean TXB2 and 6-keto-PGF1 alpha levels were highest at 48 h (22.3 and 34.2 ng X ml-1, respectively) after considerable fluctuations and with wide standard errors prior to this time. In the sponge model, however, PGE2 levels were surprisingly low for each group (mean 12.8 ng X ml-1 at 12 h) and TXB2 and 6-keto-PGF1 alpha were similarly lower (means of 3.3 and 8.1 ng X ml-1 respectively at 12 h). Mean total leucocyte counts and total protein concentrations were increased in both models after carrageenin stimulus. PGF2 alpha was not detected in measurable quantities in any exudate.(ABSTRACT TRUNCATED AT 250 WORDS)
Publication Date: 1984-03-01 PubMed ID: 6423835DOI: 10.1111/j.1365-2885.1984.tb00881.xGoogle Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research studied the presence of cyclooxygenase products of arachidonic acid metabolism in inflammation caused by carrageenin in ponies. Two different models were used and various prostaglandins and other metabolites were measured at different time intervals to understand their role during inflammation.

Research Objectives and Methodology

  • The study aimed to investigate the cyclooxygenase products of arachidonic acid metabolism in inflammation induced by carrageenin in ponies.
  • The researchers used two models for their experiments. In the first model, an inflammatory response was triggered by injecting carrageenin into polypropylene tissue cages implanted beneath the skin. The inflammation fluids, or exudates, were collected at five predetermined times between 3 and 48 hours after injection.
  • In the second model, carrageenin-impregnated polyester sponges were inserted under the skin and exudates were harvested after 6, 12, and 24 hours.
  • Both these models helped in imitating localized inflammation, allowing scientists to measure and analyze the inflammatory responses and the concentration of various arachidonic acid metabolites in them.

Measurements and Results

  • Various products like Prostaglandin E2, Thromboxane B2, and 6-Keto-Prostaglandin F1 alpha were measured in collected exudates using a method called Radio Immunoassay (RIA).
  • The RIA results showed that in Model 1, the average concentration of Prostaglandin E2 reached 197 ng per ml at 12 hours but decreased to less than 12 ng per ml at 24 hours.
  • Levels of Thromboxane B2 and 6-Keto-Prostaglandin F1 alpha were highest after 48 hours, although they showed considerable fluctuations prior to this time.
  • In the sponge model (Model 2), however, the levels of all these products were surprisingly lower, with Prostaglandin E2 averaging out to be about 12.8 ng per ml at 12 hours. The other two products also showed lower levels in this model.
  • The inflammation, in both models, led to an increase in total leucocyte counts and total protein concentrations, indicating a response to inflammation.
  • However, Prostaglandin F2 alpha was not found in measurable quantities in any exudate.

Conclusion

  • The study provides valuable insights into the role of arachidonic acid metabolites in inflammatory responses in ponies. It further emphasizes differences in their levels based on the inflammation model used. However, the complete understanding of these metabolites’ role in inflammation requires further detailed research.

Cite This Article

APA
Higgins AJ, Lees P. (1984). Arachidonic acid metabolites in carrageenin-induced equine inflammatory exudate. J Vet Pharmacol Ther, 7(1), 65-72. https://doi.org/10.1111/j.1365-2885.1984.tb00881.x

Publication

ISSN: 0140-7783
NlmUniqueID: 7910920
Country: England
Language: English
Volume: 7
Issue: 1
Pages: 65-72

Researcher Affiliations

Higgins, A J
    Lees, P

      MeSH Terms

      • 6-Ketoprostaglandin F1 alpha / analysis
      • Animals
      • Arachidonic Acid
      • Arachidonic Acids / metabolism
      • Biological Assay
      • Carrageenan
      • Dinoprostone
      • Disease Models, Animal
      • Exudates and Transudates / analysis
      • Exudates and Transudates / cytology
      • Female
      • Horses
      • Inflammation / metabolism
      • Leukocyte Count
      • Male
      • Prostaglandins E / analysis
      • Radioimmunoassay
      • Thromboxane B2 / analysis
      • Thromboxanes / analysis

      Citations

      This article has been cited 3 times.
      1. Cheng Z, Nolan AM, McKellar QA. Measurement of cyclooxygenase inhibition in vivo: a study of two non-steroidal anti-inflammatory drugs in sheep.. Inflammation 1998 Aug;22(4):353-66.
        doi: 10.1023/a:1022364731126pubmed: 9675607google scholar: lookup
      2. Cheng Z, McKellar Q, Nolan A, Lees P. Preliminary pharmacokinetic and pharmacodynamic studies on flunixin meglumine in donkeys.. Vet Res Commun 1996;20(5):469-72.
        doi: 10.1007/BF00419184pubmed: 8908727google scholar: lookup
      3. Herbort CP, Okumura A, Mochizuki M. Endotoxin-induced uveitis in the rat. A study of the role of inflammation mediators.. Graefes Arch Clin Exp Ophthalmol 1988;226(6):553-8.
        doi: 10.1007/BF02169204pubmed: 2463214google scholar: lookup