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Effects of a phenylbutazone paste in ponies: model of acute nonimmune inflammation.

Abstract: In a 12-day treatment schedule, 5 ponies were given orally a paste formulation of phenylbutazone (PBZ) and 5 matched ponies were given equivalent doses of a placebo paste. On day 12, a mild, nonimmune inflammatory reaction was induced subcutaneously in the neck of each pony by inserting sterile, polyester sponge strips soaked in a 2% carrageenan solution. Exudate was collected at 4, 8, 12, and 24 hours by serial removal of sponges. There were no significant (P less than 0.05) differences in exudate protein concentration and leukocyte numbers between the treatment groups, but the group given PBZ had significantly reduced exudate concentrations of eicosanoids 6-keto-prostaglandin F 1 alpha (the stable metabolite of prostacyclin) at 4, 8, and 12 hours; thromboxane B2 at 8, 12, and 24 hours; and bicyclic prostaglandin E2 at 8 hours. The maximal depression of eicosanoid synthesis occurred at times of peak exudate concentrations of PBZ (8 and 12 hours). Phenylbutazone was cleared more slowly from exudate than from plasma. Changes in surface skin temperature were measured by infrared thermometry. Lesional temperatures were recorded 1 cm below the base of the incision line, and mean increases were significantly (P less than 0.05) less in PBZ-treated than in placebo-treated ponies between 4 and 24 hours. The importance of the findings for the clinical efficacy of this dosage schedule is considered.
Publication Date: 1986-11-01 PubMed ID: 3466561
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research article studies the effects of a phenylbutazone paste on ponies, focusing on how it influences acute nonimmune inflammation. The paper confirms that the paste significantly reduces certain inflammation-related substances, potentially contributing to the clinical efficacy of the treatment schedule.

Research Methodology

  • The study was designed around a 12-day treatment schedule during which 5 ponies were given a paste formulation of phenylbutazone (PBZ) orally and 5 were given a placebo paste in equivalent doses.
  • On the 12th day, a mild, nonimmune inflammation was induced in each pony. This was done by inserting sterile, polyester sponge strips soaked in a 2% carrageenan solution under the skin on the ponies’ necks.
  • The exudate or fluid resulting from the inflammation was collected at 4, 8, 12, and 24 hours by removing the sponges at each time interval.

Findings

  • The research showed there were no significant differences in the concentration of protein and count of leukocyte cells in the exudate between the treatment groups. However, the group treated with PBZ exhibited significantly reduced concentrations of eicosanoids, compounds that have hormone-like effects.
  • The reduction was seen specifically in 6-keto-prostaglandin F 1 alpha (at 4, 8, and 12 hours), thromboxane B2 (at 8, 12, and 24 hours) and bicyclic prostaglandin E2 (at 8 hours). The effect was most pronounced at the peak exudate concentrations of PBZ, specifically 8 and 12 hours.
  • The findings also indicated that the PBZ was cleared more slowly from the exudate as compared to the plasma.

Additional Observations

  • Changes in the surface skin temperature of the ponies were also recorded during the course of the study. This was done by measuring the temperature 1 cm below the base of the incision line through infra-red thermometry.
  • Interestingly, the average increase in temperature was significantly lesser in ponies treated with PBZ as compared to those treated with the placebo.

Implications

  • The results of the study suggest that PBZ may contribute to the clinical efficacy of the treatment schedule. By reducing the concentrations of key compounds involved in inflammation, this medication could potentially enhance the treatment outcomes for ponies undergoing procedures that produce acute nonimmune inflammation.

Cite This Article

APA
Lees P, Higgins AJ. (1986). Effects of a phenylbutazone paste in ponies: model of acute nonimmune inflammation. Am J Vet Res, 47(11), 2359-2363.

Publication

ISSN: 0002-9645
NlmUniqueID: 0375011
Country: United States
Language: English
Volume: 47
Issue: 11
Pages: 2359-2363

Researcher Affiliations

Lees, P
    Higgins, A J

      MeSH Terms

      • 6-Ketoprostaglandin F1 alpha / analysis
      • Animals
      • Body Temperature
      • Dinoprostone
      • Disease Models, Animal
      • Exudates and Transudates / analysis
      • Female
      • Horse Diseases / drug therapy
      • Horse Diseases / metabolism
      • Horses
      • Inflammation / drug therapy
      • Inflammation / metabolism
      • Inflammation / veterinary
      • Leukocyte Count / veterinary
      • Male
      • Phenylbutazone / metabolism
      • Phenylbutazone / therapeutic use
      • Prostaglandins E / analysis
      • Thromboxane B2 / analysis

      Citations

      This article has been cited 3 times.
      1. Alquarawi AA, Ali BH. A survey of the literature (1995-1999) on the kinetics of drugs in camels (Camelus dromedarius). Vet Res Commun 2000 May;24(4):245-60.
        doi: 10.1023/a:1006498816669pubmed: 10836270google scholar: lookup
      2. Zwahlen RD, Roth DR, Wyder-Walther M. In vitro aggregation of bovine neonatal neutrophils. A comparative study with adult cattle. Inflammation 1990 Aug;14(4):375-87.
        doi: 10.1007/BF00914089pubmed: 2379953google scholar: lookup
      3. Zwahlen RD, Roth DR. Chemotactic competence of neutrophils from neonatal calves. Functional comparison with neutrophils from adult cattle. Inflammation 1990 Feb;14(1):109-23.
        doi: 10.1007/BF00914034pubmed: 2323804google scholar: lookup