Pharmacokinetics of xylazine in ponies: influence of yohimbine.
Abstract: Twenty healthy ponies were given i.v. 1.1 mg/kg of xylazine from 2 manufacturers and the pharmacokinetic parameters calculated from the disposition curves. The disposition curves for the 2 commercial preparations were not different. Yohimbine, an antagonist of the pharmacologic effects produced by xylazine, did not alter the disposition of xylazine in the plasma. A single i.v. bolus of xylazine was completely described in 17 of 20 animals by the biexponential equation: Cp = 1.30e(-0.3955t) + 0.58e(-0.033t) where Cp represents the concentration of xylazine in the plasma at time t (min). The t1/2 beta was 75 +/- 13 min and whole body clearance was 18.9 +/- 1.5 (ml/min.kg).
Publication Date: 1987-09-01 PubMed ID: 3435205
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- Journal Article
Summary
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The research article investigates the pharmacokinetics of a drug named xylazine in ponies, elaborating how its absorption, distribution, metabolism, and excretion are not affected by the presence of yohimbine, a known antagonist of xylazine.
Objective of the Research
- The main purpose of the study was to determine the pharmacokinetic parameters of xylazine, an alpha-2 adrenergic agonist often used as a sedative in veterinary medicine, in ponies and to observe if these parameters were affected by yohimbine, a common antagonist of xylazine.
Research Methodology
- Twenty healthy ponies were administered an intravenous dose of 1.1 mg/kg of xylazine from two different manufacturers.
- The disposition or distribution and elimination curves for the drug from the two manufacturers showed no significant difference, indicating that the manufacturing company did not alter the pharmacokinetics of the drug.
- The influence of yohimbine on the disposition or pharmacokinetics of xylazine was also studied. Yohimbine did not alter the pharmacokinetic behavior of xylazine in the plasma of the ponies.
- The researchers used a biexponential equation to describe the disposition of xylazine. This equation was able to accurately predict the drug levels in the plasma over time in 17 out of the 20 ponies tested.
Findings of the Study
- The study found that xylazine’s half-life (the time it takes for the concentration of the drug to reduce by half in the body) was approximately 75 minutes, with a standard deviation of 13 minutes.
- The whole-body clearance rate, indicating the body’s efficiency in metabolizing and eliminating the drug, was approximately 18.9 ml/min.kg, with a standard deviation of 1.5 ml/min.kg.
Conclusion
- Based on the findings, the study concluded that the pharmacokinetic parameters for xylazine in ponies are consistent and not influenced by the drug’s manufacturer or the presence of yohimbine.
- The findings can be applied in veterinary medicine to predict the behavior of xylazine in the pony’s body and efficiently calculate dosage requirements.
Cite This Article
APA
Dyer DC, Hsu WH, Lloyd WE.
(1987).
Pharmacokinetics of xylazine in ponies: influence of yohimbine.
Arch Int Pharmacodyn Ther, 289(1), 5-10.
Publication
Researcher Affiliations
- Department of Veterinary Physiology and Pharmacology, College of Veterinary Medicine, Iowa State University, Ames 50011.
MeSH Terms
- Animals
- Drug Interactions
- Female
- Horses / metabolism
- Injections, Intravenous / veterinary
- Male
- Thiazines / pharmacokinetics
- Xylazine / pharmacokinetics
- Yohimbine / pharmacology
Citations
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