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Equine veterinary journal1989; 21(1); 34-38; doi: 10.1111/j.2042-3306.1989.tb02086.x

Interactions between chloramphenicol, acepromazine, phenylbutazone, rifampin and thiamylal in the horse.

Abstract: The potential for interactions between chloramphenicol, phenylbutazone, acepromazine and thiamylal and chloramphenicol, rifampin, and phenylbutazone were evaluated in two groups of experiments. In the first, five horses were given thiamylal intravenously (iv) (6.6 mg/kg) after pretreatment with acepromazine, and the time of recumbency was determined. Administration of chloramphenicol iv (25 mg/kg) 1 h prior to anaesthesia significantly lengthened the recumbency time from 21.8 +/- 4.8 mins to 36.0 +/- 8.3 mins. There was an apparent but not statistically significant decrease in recumbency time when phenylbutazone (4.4 mg/kg) was administered iv daily for 4 days prior to anaesthesia. In the second series of experiments, phenylbutazone (4.4 mg/kg), chloramphenicol (25 mg/kg) and rifampin (10 mg/kg) were administered in various sequences to five different horses. Chloramphenicol pretreatment produced a significant decrease in the elimination rate and rifampin a significant increase in the elimination rate of phenylbutazone. The half-life of elimination of phenylbutazone alone was about 4 h. Following four days pretreatment with rifampin it was approximately 2.7 h, it was approximately 5.6 h and 9.5 h, respectively, when chloramphenicol was administered in one dose 1 h before or two doses 12 h and 1 h before phenylbutazone.
Publication Date: 1989-01-01 PubMed ID: 2920698DOI: 10.1111/j.2042-3306.1989.tb02086.xGoogle Scholar: Lookup
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  • Journal Article

Summary

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The research analyzes the potential interactions of certain drugs in horses, showing that chloramphenicol, in particular, can significantly influence anaesthesia duration and elimination rate of phenylbutazone.

Overview of Research

  • The study aimed to understand how certain drugs interact with each other when administered to horses – more specifically, the interactions between chloramphenicol, acepromazine, phenylbutazone, rifampin, and thiamylal.
  • Two sets of experiments were conducted to evaluate these interactions.

First Experiment

  • In the initial round of experiments, five horses were intravenously given thiamylal (an anesthetic) after pretreatment with acepromazine (a tranquilizer).
  • The primary focus here was to determine the time of recumbency, which is the period when the horse is lying down post-anesthesia.
  • The researchers found that when chloramphenicol (an antibiotic) was administered intravenously one hour prior to anesthesia, it significantly extended the recumbency period from an average of roughly 22 minutes to approximately 36 minutes.
  • Administration of phenylbutazone (a non-steroidal anti-inflammatory drug) intravenously for four days prior to anesthesia showed a decrease in recumbency time, but the decrease was not statistically significant.

Second Experiment

  • In the second round of experiments, phenylbutazone, chloramphenicol, and rifampin (an antibiotic) were administered in varying sequences to another set of five horses.
  • The goal here was to study the impact of these drug combinations on the elimination rate of phenylbutazone.
  • The results showed that pretreatment with chloramphenicol led to a significant decrease in the elimination rate of phenylbutazone, while rifampin significantly increased its elimination rate.
  • The half-life of phenylbutazone elimination alone was around 4 hours, whereas with rifampin pretreatment for four days, it fell to approximately 2.7 hours. On the contrary, it increased to nearly 5.6 hours and 9.5 hours respectively when one and two doses of chloramphenicol were administered prior to phenylbutazone.

Cite This Article

APA
Burrows GE, MacAllister CG, Tripp P, Black J. (1989). Interactions between chloramphenicol, acepromazine, phenylbutazone, rifampin and thiamylal in the horse. Equine Vet J, 21(1), 34-38. https://doi.org/10.1111/j.2042-3306.1989.tb02086.x

Publication

ISSN: 0425-1644
NlmUniqueID: 0173320
Country: United States
Language: English
Volume: 21
Issue: 1
Pages: 34-38

Researcher Affiliations

Burrows, G E
  • Department of Clinical Medicine and Surgery, College of Veterinary Medicine, Oklahoma State University, Stillwater 74078.
MacAllister, C G
    Tripp, P
      Black, J

        MeSH Terms

        • Acepromazine / pharmacokinetics
        • Acepromazine / pharmacology
        • Animals
        • Anti-Bacterial Agents / pharmacokinetics
        • Anti-Bacterial Agents / pharmacology
        • Chloramphenicol / pharmacokinetics
        • Chloramphenicol / pharmacology
        • Drug Interactions
        • Enzyme Induction
        • Female
        • Horses / metabolism
        • Male
        • Mixed Function Oxygenases / antagonists & inhibitors
        • Mixed Function Oxygenases / biosynthesis
        • Mixed Function Oxygenases / metabolism
        • Phenylbutazone / pharmacokinetics
        • Phenylbutazone / pharmacology
        • Rifampin / pharmacokinetics
        • Rifampin / pharmacology
        • Thiamylal / pharmacokinetics
        • Thiamylal / pharmacology

        Citations

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