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Xenobiotica; the fate of foreign compounds in biological systems1981; 11(5); 323-331; doi: 10.3109/00498258109045311

Studies related to the metabolism of anabolic steroids in the horse: the identification of some 16-oxygenated metabolites of testosterone and a study of the phase II metabolism.

Abstract: 1. Isomers of 3,17-dihydroxyandrostan-16-one, 3,16-dihydroxyandrostan-17-one and androstane-3,16,17-triol have been identified as urinary metabolites of testosterone in the horse. 2. Following XAD-2 extraction of urine samples, Sephadex LH-20 chromatography was used to separate the extract into conjugate groups. Metabolites obtained after hydrolysis of the conjugates have been investigated by g.l.c.-mass spectrometry. 3. Testosterone, 3,17-dihydroxyandrostan-16-one and 3,16-dihydroxyandrostan-17-one were found only in the sulphate fraction. 5 alpha-Androstane-3 beta,17 beta-diol, and two isomeric androstane triols were present mainly in this fraction and 5 alpha-androstane-3 beta,17 alpha-diol was a minor component. In the glucuronide fraction 5 alpha-androstane-3 beta,17 alpha-diol was the major metabolite present and 5 alpha-androstane-3 beta,17 beta-diol and the two isomeric triols were minor components.
Publication Date: 1981-05-01 PubMed ID: 7293223DOI: 10.3109/00498258109045311Google Scholar: Lookup
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  • Journal Article

Summary

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The research article is about how horses metabolize testosterone, an anabolic steroid, and the identification of different 16-oxygenated metabolites produced during this process.

Overview of the Research

The study primarily focusses on the identification of particular isomers of 3,17-dihydroxyandrostan-16-one, 3,16-dihydroxyandrostan-17-one, and androstane-3,16,17-triol, which were identified as urinary metabolites of testosterone in horses. These metabolites were obtained following a process of hydrolysis of the conjugates, which were separated from the urine samples using XAD-2 extraction and Sephadex LH-20 chromatography.

Methodology & Findings

  • The research employed gas-liquid chromatography and mass spectrometry for investigating these urinary metabolites of testosterone.
  • The metabolites namely, testosterone, 3,17-dihydroxyandrostan-16-one and 3,16-dihydroxyandrostan-17-one, were found only within the sulfate fraction.
  • Other metabolites including 5 alpha-Androstane-3 beta,17 beta-diol, and two isomeric androstane triols majorly fell under this fraction, and 5 alpha-androstane-3 beta,17 alpha-diol was identified as a minor component.
  • Within the glucuronide fraction, 5 alpha-androstane-3 beta,17 alpha-diol emerged as the major metabolite present.
  • In this fraction, 5 alpha-androstane-3 beta,17 beta-diol and the two isomeric triols were minor components.

Implication of the study

The findings of the study offer considerable insight into the metabolization of anabolic steroids in horses, primarily testosterone, and the resulting 16-oxygenated metabolites. These findings could be fundamental to future studies surrounding the use and effects of anabolic steroids in horses, their health, performance, and other related aspects. Understanding how these substances are metabolized in the body and the metabolites produced during the process could contribute to developing improved detection techniques for any misuse in equine sports.

Cite This Article

APA
Dumasia MC, Houghton E. (1981). Studies related to the metabolism of anabolic steroids in the horse: the identification of some 16-oxygenated metabolites of testosterone and a study of the phase II metabolism. Xenobiotica, 11(5), 323-331. https://doi.org/10.3109/00498258109045311

Publication

ISSN: 0049-8254
NlmUniqueID: 1306665
Country: England
Language: English
Volume: 11
Issue: 5
Pages: 323-331

Researcher Affiliations

Dumasia, M C
    Houghton, E

      MeSH Terms

      • Anabolic Agents / metabolism
      • Animals
      • Biotransformation
      • Horses / metabolism
      • Hydrolysis
      • Isomerism
      • Male
      • Testosterone / metabolism

      Citations

      This article has been cited 1 times.
      1. Gomes RL, Meredith W, Snape CE, Sephton MA. Analysis of conjugated steroid androgens: deconjugation, derivatisation and associated issues.. J Pharm Biomed Anal 2009 Jul 12;49(5):1133-40.
        doi: 10.1016/j.jpba.2009.01.027pubmed: 19304432google scholar: lookup