Literature DB >> 12234624

Some new aspects of 17alpha-estradiol metabolism in man.

Gerhard Hobe1, Renate Schön, Nikolai Goncharov, Gulnara Katsiya, Mikhail Koryakin, Isabelle Gesson-Cholat, Michael Oettel, Holger Zimmermann.   

Abstract

17Alpha-estradiol (1,3,5(10)-estratriene-3,17alpha-diol) together with a tracer dose of the tritium-labeled compound was administered orally and sublingually to male volunteers. The serum concentrations of 17alpha-estradiol (free and liberated by enzymatic hydrolysis) were quantified by GC/MS, and the serum total radioactivity and urinary radioactivity excretion were determined. After oral administration, 17alpha-estradiol was rapidly and intensively conjugated; only tiny quantities of the free steroid (<1% of total) appeared in serum. Sublingual administration resulted in temporary (up to 3 h p.a.) higher serum levels of the free compound. The metabolite patterns obtained by TLC of extracts from serum and urine demonstrated that 17alpha-estradiol is the subject of a poor phase I metabolism in man. A great discrepancy was found in the serum concentrations of 17alpha-estradiol (free + conjugated) determined by GC/MS and the serum radioactivity expressed in 17alpha-estradiol equivalents. By TLC analysis of the steroid conjugates extracted from serum, various 17alpha-estradiol conjugate peaks were found. By enzymatic hydrolysis with beta-glucuronidase/aryl sulfatase from Helix pomatia they were only partially cleaved. Thus, the difference between the serum radioactivity and the 17alpha-estradiol levels determined by GC/MS had to be attributed to an incomplete conjugate hydrolysis. It has been shown with the synthesized 17alpha-estradiol sulfate conjugates that only the 3-sulfate is cleaved by enzymatic hydrolysis, whereas the 17-sulfate group resists enzymatic hydrolysis. The methanolysis procedure (acetyl chloride in MeOH) has proved to be an efficient method for cleaving both the 3-sulfate group and the 17-sulfate group. In contrast to the 17alpha-estradiol conjugates in serum, the urinary conjugates were intensively split by the enzyme preparation. From this, it has to be concluded that the serum conjugates were deconjugated and newly reconjugated before urinary excretion. Copyright 2002 Elsevier Science Inc.

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Year:  2002        PMID: 12234624     DOI: 10.1016/s0039-128x(02)00058-2

Source DB:  PubMed          Journal:  Steroids        ISSN: 0039-128X            Impact factor:   2.668


  8 in total

Review 1.  Analysis of estrogens and androgens in postmenopausal serum and plasma by liquid chromatography-mass spectrometry.

Authors:  Qingqing Wang; Lisa Bottalico; Clementina Mesaros; Ian A Blair
Journal:  Steroids       Date:  2014-08-20       Impact factor: 2.668

2.  Simultaneous Measurement of 17β-Estradiol, 17α-Estradiol and Estrone by GC-Isotope Dilution MS/MS.

Authors:  Katalin Prokai-Tatrai; Darius Bonds; Laszlo Prokai
Journal:  Chromatographia       Date:  2010-02       Impact factor: 2.044

3.  Separation of dansylated 17β-estradiol, 17α-estradiol, and estrone on a single HPLC column for simultaneous quantitation by LC-MS/MS.

Authors:  Szabolcs Szarka; Vien Nguyen; Laszlo Prokai; Katalin Prokai-Tatrai
Journal:  Anal Bioanal Chem       Date:  2013-02-01       Impact factor: 4.142

Review 4.  Ultra-high sensitivity analysis of estrogens for special populations in serum and plasma by liquid chromatography-mass spectrometry: Assay considerations and suggested practices.

Authors:  Qingqing Wang; Clementina Mesaros; Ian A Blair
Journal:  J Steroid Biochem Mol Biol       Date:  2016-01-06       Impact factor: 4.292

Review 5.  Analysis of estrogens in serum and plasma from postmenopausal women: past present, and future.

Authors:  Ian A Blair
Journal:  Steroids       Date:  2010-01-28       Impact factor: 2.668

6.  In vitro inhibition of porcine cytochrome P450 by 17β -estradiol and 17α-estradiol.

Authors:  Galia Zamaratskaia; Martin Krøyer Rasmussen; Isabelle Herbin; Bo Ekstrand; Vladimir Zlabek
Journal:  Interdiscip Toxicol       Date:  2011-06

7.  Evidence that 17alpha-estradiol is biologically active in the uterine tissue: antiuterotonic and antiuterotrophic action.

Authors:  Mercedes Perusquía; Erika Navarrete
Journal:  Reprod Biol Endocrinol       Date:  2005-07-21       Impact factor: 5.211

8.  Male lifespan extension with 17-α estradiol is linked to a sex-specific metabolomic response modulated by gonadal hormones in mice.

Authors:  Michael Garratt; Kim A Lagerborg; Yi-Miau Tsai; Andrzej Galecki; Mohit Jain; Richard A Miller
Journal:  Aging Cell       Date:  2018-05-27       Impact factor: 9.304

  8 in total

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