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The Journal of Clinical Endocrinology & Metabolism Vol. 86, No. 1 146-150
Copyright © 2001 by The Endocrine Society


Original Studies

Urinary Nandrolone Metabolites of Endogenous Origin in Man: A Confirmation by Output Regulation under Human Chorionic Gonadotropin Stimulation

Yves Reznik, Louis Dehennin, Christine Coffin, Jacques Mahoudeau and Pierre Leymarie

Service d’Endocrinologie (Y.R., C.C., J.M.) and Laboratoire de Biochimie B (P.L.) Centre Hospitalier Universitaire Côte de Nacre 14033 Caen; and Laboratoire de la Fédération Nationale des Courses Françaises (L.D.), 92290 Chatenay-Malabry, France

Address all correspondence and requests for reprints to: Y. Reznik, M.D., Department of Endocrinology, Centre Hospitalier Universitaire Côte de Nacre, 14033 Caen Cedex, France.

19-Nortestosterone (nandrolone) is an anabolic steroid compound widely used as a doping agent by athletes. The analysis of its urinary metabolites, 19-norandrosterone (NA) and 19-noretiocholanolone (NE) glucuronides, allows the detection of surreptitious administration of nandrolone in sport. A threshold concentration at 2 µg/L urinary nandrolone metabolites is advocated by the International Olympic Committee for the detection of doping, but some controversy concerning the validity of this threshold arose from the demonstration of endogenous production of nandrolone in mammals, including humans. The regulation of human nandrolone production and its contribution in vivo to the process of aromatization remain unknown. In the present study 10 healthy men were successively submitted to insulinic stress and gonadal stimulation by hCG administration. Urinary NA and NE concentrations were quantified by gas chromatography-mass spectrometry. NA was detected in basal urine samples from all subjects, with a mean urinary excretion rate (UER) of 3.17 ± 0.35 ng/h, whereas NE was detected in 4 of 10 (UER range, 0.8–4.7 ng/h). Insulinic hypoglycemia did not significantly modify mean NA UER despite random intraindividual variations between timed urine collections. After hCG administration, NA UER increased by 250% (P < 0.01) and estradiol (E2) UER by 260% (P < 0.001). The maximum NA concentration obtained after stimulation was 0.43 µg/L. NA UER, plasma E2, and E2/T ratio peaked on day 1 after hCG administration, whereas plasma T peaked later on day 3. NA UER correlated with plasma E2 (r = 0.61; P < 0.001) and E2/T (r = 0.51; P < 0.001), but not with plasma T. In conclusion, insulinic stress did not significantly alter nandrolone metabolism, whereas the effect of hCG was a stimulation of NA excretion in all subjects, which constitutes strong support for the endogenous origin of low basal NA excretion. The comparative kinetics of NA UER, plasma E2, and E2/T ratio suggest a contribution of the aromatase process to nandrolone biosynthesis in man.




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