En vigueur

Metabolism and Excretion of 3,6,17- Androstenetrione

Investigateur principal
F. Delbeke
Pays
Belgique
Institution
Ghent University
Année approuvée
2003
Statut
Complété
Themes
Stéroïdes anabolisants

Description du projet

Code: 03B06FD 

3,6,17-androstenetrione is an anabolic steroid and is also referred to as 6-oxo. This product is sold as an over the counter product in the United States where it is regarded as a nutritional supplement. It is widely available on the internet and it is marketed as an antiestrogenic agent. Athletes might be tempted to threat the adverse effects of an extensive abuse of anabolic steroids (e.g. suppression of androgens and gynaecomastia) by using this type of drugs. Although at present no results from clinical studies supporting the claims of the manufacturer are available, it seems likely that athletes will use this product. This is especially true because the manufacturer of this product is the same company that introduced 1 -androstenediol, 4- androstenedione, 4-androstenediol and 1 9-nor-4-androstenediol on the prohormone market. All of these products have rapidly become a commercial succes. Although the manufacturer claims that 6-oxo is the natural first antiestrogenic product, it is clear that based upon its structure this product can be regarded as an anabolic steroid as well. The producer claims that 6-oxo works as an aromatase inhibitor, blocking the aromatisation of endogenous as well as exogenously administered drugs resulting in higher levels of endogenous steroids as well as synthetic co-administered steroids. Based upon its structure, it is likely that 6-oxo is not metabolised into endogenous steroids commonly screened for during doping control, misuse of this substance remains undetected. It seems therefore necessary to determine whether or not the use of this supplement does indeed result in higher levels of endogenous steroids (testosterone). Moreover elucidation of the metabolism and identification of 6-oxo metabolites is necessary to allow for the detection of this supplement. This research would therefore investigate the metabolism and excretion of 6-oxo to allow for its detection in the urine of athletes.

Main Findings: 

The analysis of the 6-OXO supplement resulted in the detection of 6-oxo-androstenedione but also of 6b-OH-androstenedione. No other contaminants were detected. Excretion studies resulted in the detection of the parent drug 6-oxo-androstenedione and 6a-OH-androstenedione and 6a-OH-testosterone as metaboites. A GC-MS-SIM method was developed and validated to fulfil requirements of WADA for doping control laboratories. Using this method, the ingestion of the supplement, accordin the manufacturers recommendations resulted in the detection of a 6a-OH-androstenedione up to 37 h after the administration, while 6-oxo-androstenedione and 6a-OH-testosterone could be detected up to 24h post administration. Because of the longer detection time and its presence in urine after administration of androstenedione, it is recmmended that beides 6-oxo-androstenedione, 6a-OH-androstenedione is also included in screening methods for doping control purposes. The presence of 6-oxo-androstenedione or 6a-OH-testosterone can be used to disciminate between the administration of 6-oxo-androstenedione and androstenedione