Cited by 40Steroid Chemistry and BiochemistryHormonal and reproductive studiesPharmacogenetics and Drug Metabolism

Detection, synthesis and characterization of metabolites of steroid hormones conjugated with cysteine

Fabregat, Andreu, Kotronoulas, Aristotelis, Marcos, Josep, Joglar, Jesús, Alfonso, Ignacio, Segura, Jordi, Ventura, Rosa, Pozo, Oscar J.·2013·Steroids

Abstract

The occurrence of several polyunsaturated testosterone related compounds (including 4,6-androstadien-3,17-dione and 4,6-androstadien-17β-ol-3-one) in urine after alkaline treatment of the sample has been recently reported. Although several experiments seem to indicate that they are testosterone metabolites, their origin is still unknown. In this study, it is demonstrated that these metabolites are produced from the degradation of cysteine conjugates. Several testosterone metabolites conjugated with cysteine have been synthesized and characterized by NMR techniques. Their detection in human urine has been performed by LC-MS/MS. The acquisition of several transitions in the SRM mode and the comparison between ion ratios and retention times allowed for the unequivocal confirmation of the presence of cysteine conjugates in urine. The analysis of urine samples collected after testosterone administration confirmed that synthesized cysteine conjugates are testosterone metabolites. The fact that these conjugates result in polyunsaturated compounds in urine after alkaline treatment was demonstrated by fraction collection and alkaline treatment of each fraction. Besides, the presence of these metabolites was also confirmed in human plasma. The formation of these metabolites implies an unreported metabolic biotransformation: 6,7-dehydrogenation as phase I metabolism followed by conjugation with glutathione and subsequent transformation to cysteine conjugates. Finally, the existence of similar metabolites for cortisol and progesterone was also confirmed by LC-MS/MS indicating that the presented metabolic pathway is not exclusively active in androgens, but common to progestagens and glucocorticoids.

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Crossref · 10.1016/j.steroids.2012.11.017

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  • Besides the classical conjugates, T metabolites conjugated with cysteine have been detected in urine and plasma.

    “Besides the classical conjugates, T metabolites conjugated with cysteine have been detected in urine and plasma (Fabregat et al., 2013).”

    From Intracrine androgen biosynthesis, metabolism and action revisited (2018) · cites this paper as Fabregat et al., 2013

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Authors
Fabregat, A., Kotronoulas, A., Marcos, J., Joglar, J., Alfonso, I., Segura, J., Ventura, R., & Pozo, O. J.
Affiliations
  • Municipal Institute for Medical Research (ES)
  • Consejo Superior de Investigaciones Científicas (ES)
  • Universitat Pompeu Fabra (ES)
Venue
Steroids
Publisher
Elsevier BV
Published
2013-03
Volume
78
Issue
3
Pages
327-336
ISSN
0039-128X (ISSN-L)
OpenAlex
W2012001747
Cited by
40
References
36
Citations by year
2025: 1 · 2024: 2 · 2023: 5 · 2021: 2 · 2020: 1 · 2019: 2 · 2018: 3 · 2017: 6 · 2016: 2 · 2015: 8 · 2014: 3 · 2013: 5
FWCI
2.05
Type
journal article
Language
en
Open access
closed
Locations
  • Steroids (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Generalitat de Catalunya
  • Instituto de Salud Carlos III
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Steroid Chemistry and Biochemistry
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Hormonal and reproductive studies
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Pharmacogenetics and Drug Metabolism
Keywords
testosterone metabolites, cysteine conjugates, glutathione conjugation, phase I biotransformation, steroid metabolism, cortisol metabolites, progesterone metabolites, human urine, human plasma, alkaline hydrolysis
MeSH terms
Androstadienes, Biotransformation, Chromatography, Liquid, Cysteine, Glutathione, Humans, Hydrocortisone, Hydroxides, Models, Molecular, Progesterone, Testosterone, Potassium Compounds, Metabolic Detoxication, Phase II, Tandem Mass Spectrometry

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