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Effects of a histamine type 2 receptor antagonist, BMY-26539-01, on equine gastric acid secretion.

Abstract: A dose-response study was undertaken of the effects of a newly developed histamine type 2 receptor antagonist, BMY-26539-01, on gastric acid secretion in 4 fasted horses. Doses of 0.1 mg/kg, 0.3 mg/kg, 0.5 mg/kg, or placebo were administered in a randomly assigned treatment sequence. Hydrogen ion concentration and pH were variable during baseline measurements in all 4 animals; however, following BMY-26539-01 administration, mean pH increased and hydrogen ion concentration decreased in a dose-related pattern. At the 0.3 mg/kg and 0.5 mg/kg dose levels, pH remained elevated for > 4 h and > 8 h, respectively. No adverse effects were observed. A significant level of 0.01 was used for all statistical methods.
Publication Date: 2001-03-03 PubMed ID: 11227196PubMed Central: PMC1189643
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  • Clinical Trial
  • Journal Article
  • Randomized Controlled Trial

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

This research studied the effects of a new histamine type 2 receptor antagonist (BMY-26539-01) on gastric acid secretion in horses. It found that the medicine increased the pH and decreased the hydrogen ion concentration in the horses’ stomachs in a dose-related schedule, with no adverse outcomes recorded.

Study Design

  • The research aimed to test the impacts of BMY-26539-01, a newly created histamine type 2 receptor antagonist, on gastric acid release in fasted horses. The study was designed as a dose-response study where varying doses of the drug were administered to test its efficacy.
  • The experiment was conducted on four fasted horses, and different doses of BMY-26539-01 (0.1 mg/kg, 0.3 mg/kg, 0.5 mg/kg) or a placebo were given in a randomly determined sequence to each horse.

Measurements and Results

  • Through baseline measurements, the researchers observed that the hydrogen ion concentration and pH levels fluctuated in all four horses before the drug administration.
  • However, following the administration of BMY-26539-01, the average pH levels in the horses went up, and the hydrogen ion concentration fell, and these changes followed a dose-related pattern. This means that higher doses of BMY-26539-01 caused a greater increase in pH level and a larger decrease in hydrogen ion concentration.
  • At the doses of 0.3 mg/kg and 0.5 mg/kg, the increased pH levels persisted for greater than 4 hours and 8 hours respectively. This demonstrates that the drug’s effect was not only evident but also long-lasting.
  • The study recorded no adverse effects from the administration of BMY-26539-01, suggesting that it is safe for use in horses.
  • All statistical methods used in the study had a significant level of 0.01. This means that there was only a 1 percent chance that the results obtained were due to random occurrence, thus confirming the accuracy of the findings.

Significance of the Research

  • This research provides promising evidence for the efficacy and safety of BMY-26539-01 in controlling gastric acid secretion in horses. The drug can potentially serve as an effective treatment for equine gastric problems, specifically those involving excessive gastric acid secretion.
  • The significant level used for all statistical methods implies that the probability of the observed results being due to mere chance is very low. Therefore, the findings of the research carry a high level of reliability and validity.

Cite This Article

APA
Orsini JA, Spencer PA. (2001). Effects of a histamine type 2 receptor antagonist, BMY-26539-01, on equine gastric acid secretion. Can J Vet Res, 65(1), 55-59.

Publication

ISSN: 0830-9000
NlmUniqueID: 8607793
Country: Canada
Language: English
Volume: 65
Issue: 1
Pages: 55-59

Researcher Affiliations

Orsini, J A
  • Department of Clinical Studies, School of Veterinary Medicine, University of Pennsylvania, New Bolton Center, Kennett Square 19348, USA. orsini@vet.upenn.edu
Spencer, P A

    MeSH Terms

    • Animals
    • Dose-Response Relationship, Drug
    • Female
    • Gastric Acid / metabolism
    • Histamine H2 Antagonists / administration & dosage
    • Histamine H2 Antagonists / pharmacology
    • Horses / metabolism
    • Hydrogen-Ion Concentration
    • Receptors, Histamine H2
    • Time Factors

    References

    This article includes 17 references
    1. Auguste LJ, Angus L, Stein TA, Wise L. Starvation and mucosal prostaglandin-E2 in gastric stress ulceration.. Crit Care Med 1988 Jun;16(6):610-1.
    2. Baker SJ, Gerring EL. Effects of single intravenously administered doses of omeprazole and ranitidine on intragastric pH and plasma gastrin concentration in nonfed ponies.. Am J Vet Res 1993 Dec;54(12):2068-74.
      pubmed: 8116940
    3. Dragstedt LR. On the cause of gastric and duodenal ulcers.. J R Coll Surg Edinb 1971 Sep;16(5):251-63.
      pubmed: 5115272
    4. MacKay RJ, French TW, Nguyen HT, Mayhew IG. Effects of large doses of phenylbutazone administration to horses.. Am J Vet Res 1983 May;44(5):774-80.
      pubmed: 6869982
    5. Hammond CJ, Mason DK, Watkins KL. Gastric ulceration in mature thoroughbred horses.. Equine Vet J 1986 Jul;18(4):284-7.
    6. Campbell-Thompson ML, Merritt AM. Effect of ranitidine on gastric acid secretion in young male horses.. Am J Vet Res 1987 Oct;48(10):1511-5.
      pubmed: 3674562
    7. Parmar NS, Tariq M, Ageel AM. Studies on the possible mechanism of morphine-induced potentiation of the gastroulcerogenic effect of indomethacin in rats.. Arch Int Pharmacodyn Ther 1987 Sep;289(1):149-60.
      pubmed: 3435201
    8. Levine BA. Pathophysiology and mechanisms of stress ulcer injury.. Pharmacotherapy 1987;7(6 Pt 2):90S-94S.
    9. Traub-Dargatz JL, Bertone JJ, Gould DH, Wrigley RH, Weiser MG, Forney SD. Chronic flunixin meglumine therapy in foals.. Am J Vet Res 1988 Jan;49(1):7-12.
      pubmed: 3354970
    10. Aoki T. Treatment of upper gastro-intestinal bleeding with the H2-receptor antagonist famotidine.. J Int Med Res 1989;17 Suppl 1:32A-40A.
      pubmed: 2566542
    11. Meschter CL, Gilbert M, Krook L, Maylin G, Corradino R. The effects of phenylbutazone on the morphology and prostaglandin concentrations of the pyloric mucosa of the equine stomach.. Vet Pathol 1990 Jul;27(4):244-53.
      pubmed: 2402852doi: 10.1177/030098589002700405google scholar: lookup
    12. Orsini JA, Dreyfuss DJ, Vecchione J, Spencer PA, Uhlman R. Effects of a histamine type-2 receptor antagonist (BMY-25368) on gastric secretion in horses.. Am J Vet Res 1991 Jan;52(1):108-10.
      pubmed: 1673593
    13. MacAllister CG, Sangiah S, Mauromoustakos A. Effect of a histamine H2 type receptor antagonist (WY 45, 727) on the healing of gastric ulcers in ponies.. J Vet Intern Med 1992 Sep-Oct;6(5):271-5.
    14. Pfeiffer CJ. A review of spontaneous ulcer disease in domestic animals: chickens, cattle, horses, and swine.. Acta Physiol Hung 1992;80(1-4):149-58.
      pubmed: 1345182
    15. Murray MJ, Grodinsky C. Regional gastric pH measurement in horses and foals.. Equine Vet J Suppl 1989 Jun;(7):73-6.
    16. Furr MO, Murray MJ. Treatment of gastric ulcers in horses with histamine type 2 receptor antagonists.. Equine Vet J Suppl 1989 Jun;(7):77-9.
    17. Kleiman RL, Adair CG, Ephgrave KS. Stress ulcers: current understanding of pathogenesis and prophylaxis.. Drug Intell Clin Pharm 1988 Jun;22(6):452-60.
      pubmed: 3293957doi: 10.1177/106002808802200602google scholar: lookup

    Citations

    This article has been cited 1 times.
    1. Kong L, Domarecka E, Szczepek AJ. Histamine and Its Receptors in the Mammalian Inner Ear: A Scoping Review. Brain Sci 2023 Jul 20;13(7).
      doi: 10.3390/brainsci13071101pubmed: 37509031google scholar: lookup