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Journal of veterinary internal medicine2013; 27(5); 1185-1192; doi: 10.1111/jvim.12153

Pharmacodynamic evaluation of 4 angiotensin-converting enzyme inhibitors in healthy adult horses.

Abstract: Angiotensin-converting enzyme (ACE) inhibitors are used in horses with cardiovascular disorders despite the paucity of available data regarding their efficacy. Objective: The degree of serum ACE inhibition varies considerably between drugs. Methods: Eight healthy adult horses. Methods: Randomized prospective study. Horses were fasted overnight prior to receiving one of 4 ACE inhibitors intragastrically, administered at one of 2 dosages, using a randomized Latin square design (benazepril: 0.5 and 0.25 mg/kg; ramipril: 0.3 and 0.1 mg/kg; quinapril: 0.25 and 0.125 mg/kg; perindopril: 0.1 and 0.05 mg/kg). Serum ACE activity was measured using a kinetic spectrophotometric method. Results: There was a significant effect of drug and dosage on maximum ACE inhibition (I(max)), ACE inhibition 24 hours after administration (I(24h)), and area under the curve (AUC(0-48h)). Benazepril at 0.5 mg/kg resulted in significantly higher I(max) (86.9 ± 7.0%) and I(24h) (60.3 ± 7.9%) compared to the other drugs. There was a significant decrease in indirect blood pressure (BP) over time after administration of each drug, but differences in BP were not significantly different between drugs. Pharmacodynamic variables measured after administration of benazepril to horses with free access to hay were not significantly different from those obtained after fasting. Administration of benazepril orally once daily for 7 days did not result in a cumulative effect on ACE inhibition. Conclusions: Of the ACE inhibitors tested, oral benazepril (0.5 mg/kg) is the most effective at inhibiting serum ACE activity in healthy horses.
Publication Date: 2013-08-19 PubMed ID: 23952255DOI: 10.1111/jvim.12153Google Scholar: Lookup
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  • Journal Article
  • Randomized Controlled Trial
  • Research Support
  • Non-U.S. Gov't

Summary

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This study focuses on testing the efficacy of four different angiotensin-converting enzyme (ACE) inhibitors in horses, with results showing that benazepril was the most effective at inhibiting ACE activity.

Study Objective and Methodology

  • The study aims to analyze how serum ACE inhibition differs among four ACE inhibitors, due to the limited available data on their efficacy in horses. The experiment involved healthy adult horses and had a prospective, randomized design for control and consistency.
  • Focusing on a Latin square design, horses were given one of the four ACE inhibitors via an intragastric route, at one of two doses. The ACE inhibitors used were benazepril, ramipril, quinapril, and perindopril.
  • The activity of the serum ACE was observed using a kinetic spectrophotometric method, which measures the changes in the color intensity of a solution.

Results and Findings

  • The study found that both the type of drug and its dosage have a considerable impact on ACE inhibition, measured by maximum ACE inhibition (I(max)), ACE inhibition 24 hours post-administration (I(24h)), and the area under the curve (AUC(0-48h)).
  • Benazepril, specifically at the high dosage of 0.5 mg/kg, resulted in significantly higher I(max) and I(24h) compared to the other three drugs investigated in the study.
  • All drugs leads to a significant decrease in indirect blood pressure over time after administration. However, the differences in blood pressure reduction were not significantly different between the drugs.
  • The pharmacodynamic variables, measures after administering benazepril to horses which were not fasting, were not significantly different from those seen after fasting.
  • Giving benazepril orally every day for a week did not result in a cumulative effect on ACE inhibition.

Concluding Remarks

  • Based on the study’s findings, benazepril presented as the most effective ACE inhibitor at the given dosage (0.5 mg/kg) in inhibiting serum ACE activity in healthy horses.
  • However, more comprehensive studies might be needed to determine the long-term benefits and potential side effects of benazepril and other ACE inhibitors in horses. Also, studies should explore their effectiveness in horses with cardiovascular disorders.

Cite This Article

APA
Afonso T, Giguère S, Rapoport G, Berghaus LJ, Barton MH, Coleman AE. (2013). Pharmacodynamic evaluation of 4 angiotensin-converting enzyme inhibitors in healthy adult horses. J Vet Intern Med, 27(5), 1185-1192. https://doi.org/10.1111/jvim.12153

Publication

ISSN: 1939-1676
NlmUniqueID: 8708660
Country: United States
Language: English
Volume: 27
Issue: 5
Pages: 1185-1192

Researcher Affiliations

Afonso, T
  • Department of Large Animal Medicine, College of Veterinary Medicine, University of Georgia, Athens, GA.
Giguère, S
    Rapoport, G
      Berghaus, L J
        Barton, M H
          Coleman, A E

            MeSH Terms

            • Angiotensin-Converting Enzyme Inhibitors / pharmacokinetics
            • Angiotensin-Converting Enzyme Inhibitors / pharmacology
            • Animals
            • Area Under Curve
            • Blood Pressure / drug effects
            • Food Deprivation
            • Half-Life
            • Horses

            Citations

            This article has been cited 1 times.
            1. Agne GF, Jung SW, Wooldridge AA, Duran SH, Ravis W, Toribio R. Pharmacokinetic and pharmacodynamic properties of orally administered torsemide in healthy horses. J Vet Intern Med 2018 Jul;32(4):1428-1435.
              doi: 10.1111/jvim.15213pubmed: 29770976google scholar: lookup