Metabolic studies of mesterolone in horses
Publication in refereed journal


Times Cited
Web of Science20WOS source URL (as at 29/06/2020) Click here for the latest count
Altmetrics Information
.

Other information
AbstractMesterolone (1 alpha-methyl-5 alpha-androstan-17 beta-ol-3-one) is a synthetic anabolic androgenic steroid (AAS) with reported abuses in human sports. As for other AAS, mesterolone is also a potential doping agent in equine sports. Metabolic studies on mesterolone have been reported for humans, whereas little is known about its metabolic fate in horses. This paper describes the studies of both the in vitro and in vivo metabolism of mesterolone in racehorses with an objective to identify the most appropriate target metabolites for detecting mesterolone administration. In vitro biotransformation studies of mesterolone were performed by incubating the steroid with horse liver microsomes. Metabolites in the incubation mixture were isolated by liquid-liquid extraction and analysed by gas chromatography-mass spectrometry (GC-MS) after acylation or silylation. Five metabolites (M1-M5) were detected. They were 1 alpha-methyl-5 alpha-androstan-3 alpha-ol-17-one (M1), 1 alpha-methyl-5 alpha-androstan-3 beta-ol-17one (M2). 1 alpha-methyl-5 alpha-androstane-3 alpha,17 beta-diol (M3), 1 alpha-methyl-5 alpha-androstane-3 beta,17 beta-diol (M4), and 1 alpha-methyl-5 alpha-androstane-3,17 beta-dione (M5). Of these in vitro metabolites, M1, M3, M4 and M5 were confirmed using authentic reference standards. M2 was tentatively identified by mass spectral comparison to M1. For the in vivo metabolic studies, Proviron((R)) (20 tablets x 25 mg of mesterolone) was administered orally to two thoroughbred geldings. Pre-and post-administration urine samples were collected for analysis. Free and conjugated metabolites were isolated using solid-phase extraction and analysed by GC-MS as described for the in vitro studies. The results revealed that mesterolone was extensively metabolised and the parent drug was not detected in urine. Three metabolites detected in the in vitro studies, namely M1, M2 and M4, were also detected in post-administration urine samples. In addition. two stereoisomers each of 1 alpha-methyl-5 alpha-androstane-3,17 beta-diol (M6 and M7) and 1 alpha-methyl-5 alpha-androstane-3,16-diol17-one (M8 and N19). and an 18-hydroxylated metabolite 1 alpha-methyl-5 alpha-androstane-3,18-diol-17-one (M10) were also detected. The metabolic pathway for mesterolone is postulated. These studies have shown that metabolites M8, M9 and M10 could be used as potential screening targets for controlling the misuse of mesterolone in horses. (c) 2007 Elsevier B.V. All rights reserved.
All Author(s) ListHo ENM, Leung DKK, Leung GNW, Wan TSM, Wong HNC, Xu XH, Yeung JHK
Journal nameAnalytica Chimica Acta
Year2007
Month7
Day16
Volume Number596
Issue Number1
PublisherELSEVIER SCIENCE BV
Pages149 - 155
ISSN0003-2670
eISSN1873-4324
LanguagesEnglish-United Kingdom
Keywordsgas chromatography-mass spectrometry (GC-MS); horse; mesterolone; metabolism; steroids
Web of Science Subject CategoriesChemistry; Chemistry, Analytical; CHEMISTRY, ANALYTICAL

Last updated on 2020-30-06 at 05:23