Literature DB >> 16123077

5 Beta-dihydroprogesterone and steroid 5 beta-reductase decrease in association with human parturition at term.

Penelope M Sheehan1, Gregory E Rice, Eric K Moses, Shaun P Brennecke.   

Abstract

The role of progesterone withdrawal in human parturition continues to provoke controversy. One possible mechanism by which functional progesterone withdrawal may be achieved is by a decrease in the circulating concentration of its bioactive metabolites. The progesterone metabolite 5beta-dihydroprogesterone (5betaDHP) has been shown to be a potent tocolytic in vitro. We quantified plasma concentrations of 5betaDHP in association with the onset of spontaneous labour in women at term and steroid 5beta-reductase mRNA expression in placenta, myometrium, chorion and amnion in relation to parturition, using real time RT-PCR. Serial blood samples were obtained from patients late in pregnancy, before term labour, during term labour and within the first 24 h postpartum. Following organic solvent extraction, steroids including 5betaDHP were separated by high-performance liquid chromatography (HPLC) and then quantified by radioimmunoassay (RIA). 5betaDHP concentration decreased two-fold (P = 0.00001, n = 25) from 0.317 +/- 0.039 nmol/ml to 0.178 +/- 0.017 nmol/ml in association with active labour. Tissue 5beta-reductase mRNA-relative abundance was determined in placenta, myometrium, chorion and amnion obtained from labouring and non-labouring women. In placenta and myometrium, relative expression decreased significantly in association with labour, by about two-fold and 10-fold, respectively. These data are consistent with a possible role for 5betaDHP in the onset of spontaneous human labour. Further studies exploring this hitherto unrecognized endocrinological pathway are indicated.

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Year:  2005        PMID: 16123077     DOI: 10.1093/molehr/gah201

Source DB:  PubMed          Journal:  Mol Hum Reprod        ISSN: 1360-9947            Impact factor:   4.025


  12 in total

1.  Decreased DNA Methylations at the Progesterone Receptor Promoter A Induce Functional Progesterone Withdrawal in Human Parturition.

Authors:  Xia Li; Cheng Chen; Hui Luo; Jennifer C van Velkinburgh; Bing Ni; Qing Chang
Journal:  Reprod Sci       Date:  2014-01-08       Impact factor: 3.060

2.  Human and murine steroid 5β-reductases (AKR1D1 and AKR1D4): insights into the role of the catalytic glutamic acid.

Authors:  Mo Chen; Phumvadee Wangtrakuldee; Tianzhu Zang; Ling Duan; Laura L Gathercole; Jeremy W Tomlinson; Trevor M Penning
Journal:  Chem Biol Interact       Date:  2019-03-28       Impact factor: 5.192

Review 3.  Structural and Functional Biology of Aldo-Keto Reductase Steroid-Transforming Enzymes.

Authors:  Trevor M Penning; Phumvadee Wangtrakuldee; Richard J Auchus
Journal:  Endocr Rev       Date:  2019-04-01       Impact factor: 19.871

4.  Conversion of human steroid 5β-reductase (AKR1D1) into 3β-hydroxysteroid dehydrogenase by single point mutation E120H: example of perfect enzyme engineering.

Authors:  Mo Chen; Jason E Drury; David W Christianson; Trevor M Penning
Journal:  J Biol Chem       Date:  2012-03-20       Impact factor: 5.157

5.  Substrate specificity and inhibitor analyses of human steroid 5β-reductase (AKR1D1).

Authors:  Mo Chen; Jason E Drury; Trevor M Penning
Journal:  Steroids       Date:  2011-01-19       Impact factor: 2.668

6.  Stereospecific reduction of 5β-reduced steroids by human ketosteroid reductases of the AKR (aldo-keto reductase) superfamily: role of AKR1C1-AKR1C4 in the metabolism of testosterone and progesterone via the 5β-reductase pathway.

Authors:  Yi Jin; A Clementina Mesaros; Ian A Blair; Trevor M Penning
Journal:  Biochem J       Date:  2011-07-01       Impact factor: 3.857

Review 7.  5β-Reduced steroids and human Δ(4)-3-ketosteroid 5β-reductase (AKR1D1).

Authors:  Mo Chen; Trevor M Penning
Journal:  Steroids       Date:  2014-02-08       Impact factor: 2.668

8.  In-Depth Dissection of the P133R Mutation in Steroid 5β-Reductase (AKR1D1): A Molecular Basis of Bile Acid Deficiency.

Authors:  Mo Chen; Yi Jin; Trevor M Penning
Journal:  Biochemistry       Date:  2015-10-06       Impact factor: 3.162

9.  Rate of steroid double-bond reduction catalysed by the human steroid 5β-reductase (AKR1D1) is sensitive to steroid structure: implications for steroid metabolism and bile acid synthesis.

Authors:  Yi Jin; Mo Chen; Trevor M Penning
Journal:  Biochem J       Date:  2014-08-15       Impact factor: 3.857

Review 10.  Role of aldo-keto reductase family 1 (AKR1) enzymes in human steroid metabolism.

Authors:  Tea Lanišnik Rižner; Trevor M Penning
Journal:  Steroids       Date:  2013-11-01       Impact factor: 2.668

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