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Pharmacokinetics of small doses of 3-methylindole given to horses.

Abstract: The pharmacokinetics of 3-methylindole (3MI) given orally in 2 doses (10 mg/kg and 20 mg/kg) to horses were determined. The pharmacokinetic plasma-concentration profiles for 3MI (10- and 20-mg/kg dosages) in horses were represented by a 2-compartment open model with first-order absorption, as determined by nonlinear least-squares regression analysis. Absorption of 3MI at both dosages was rapid. Comparisons of the peak plasma concentrations, the postdistribution half lives, total clearances, and areas under the curve of the plasma-concentration profiles between the 10- and the 20-mg/kg dosages may indicate the presence of nonlinear or dose-dependent kinetics for 3MI in horses.
Publication Date: 1985-08-01 PubMed ID: 4037486
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  • Journal Article

Summary

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The research focuses on the investigation of how horses’ bodies process small amounts of 3-methylindole (3MI) administered orally, and suggests that the pharmacokinetics of 3MI might depend on the dosage given. The study assessed two different dosages — 10 mg/kg and 20 mg/kg.

Methodology

  • The researchers orally administered two different doses of 3-methylindole (3MI) — 10 mg/kg and 20 mg/kg — to horses.
  • They subsequently analyzed the plasma-concentration profiles for both dosages. The profiles were represented by a two-compartment open model (a pharmacokinetic model that assumes the body consists of two compartments: central and peripheral) with first-order absorption. This was determined through a nonlinear least-squares regression analysis, a statistical method used to fit a function to data.

Findings

  • The absorption of 3MI, for both dosages, was observed to be rapid.
  • Comparisons were made between the pharmacokinetic properties — peak plasma concentrations (the highest concentration of a drug recorded in the bloodstream after administration), postdistribution half-lives (the time taken for the drug concentration to halve after distribution phase), total clearances (the volume of blood or plasma from which the drug is completely removed per unit time), and areas under the curve of plasma-concentration profiles — for both the 10mg/kg and 20mg/kg doses.
  • The results of these comparisons suggested the possibility of nonlinear or dose-dependent kinetics for 3MI in horses, meaning that the way the compound is metabolized, distributed, and excreted could depend on the dose.

Implications

  • This research adds to the understanding of how different doses of 3MI are metabolized in horses. Such knowledge can contribute to determining the optimal dosage regimes for therapeutic or research applications utilizing 3MI.
  • If 3MI does demonstrate dose-dependent kinetics in horses, further investigations are needed to adequately characterize these kinetics and to establish accurate dose guidelines.

Cite This Article

APA
Thomas DE, Beadle RE. (1985). Pharmacokinetics of small doses of 3-methylindole given to horses. Am J Vet Res, 46(8), 1619-1624.

Publication

ISSN: 0002-9645
NlmUniqueID: 0375011
Country: United States
Language: English
Volume: 46
Issue: 8
Pages: 1619-1624

Researcher Affiliations

Thomas, D E
    Beadle, R E

      MeSH Terms

      • Administration, Oral
      • Animals
      • Biological Availability
      • Body Weight
      • Chromatography, Gas
      • Female
      • Half-Life
      • Horses / metabolism
      • Indoles / metabolism
      • Intubation, Gastrointestinal / veterinary
      • Kinetics
      • Male
      • Models, Biological
      • Regression Analysis
      • Skatole / administration & dosage
      • Skatole / blood
      • Skatole / metabolism

      Citations

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