Biosynthesis of 3 beta-hydroxy-5,7-pregnadien-20-one by the horse fetal gonad.
Abstract: The production of equilin and the other ring B-unsaturated estrogens by the pregnant mare is anomalous in that they are biosynthesised by a cholesterol-independent pathway. Fetal horse gonads were incubated with tritiated sodium acetate and radiochemically pure 3 beta-hydroxy-5,7-pregnadien-20-one and 3 beta-hydroxy-5,7-androstadien-17-one were isolated. A fetal gonad--placental system is proposed for equilin production, 3 beta-hydroxy-5,7-pregnadien-20-one being a precursor for 3 beta-hydroxy-5,7-androstadien-17-one in the fetal gonad and the latter being the precursor of equilin in the placenta. The nature of the possible precursor of 3 beta-hydroxy-5,7-pregnadien-20-one is discussed.
Publication Date: 1983-03-07 PubMed ID: 6219005DOI: 10.1016/0014-5793(83)80139-2Google Scholar: Lookup
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Summary
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This study analyses the unique process in which pregnant horses produce the estrogen hormone elevin and other similar hormones. Using radioactive labelling techniques, the research shows that these hormones are created through a pathway distinct from the typical cholesterol-derived process seen in most mammals. It suggests an interplay between the horse’s fetal gonad and the placenta in hormone synthesis.
Unique Biosynthesis Pathway in Pregnant Mares
- The research highlights an unique aspect of pregnant mare’s hormonal system, where estrogens like elevin are synthesized not from cholesterol, a common precursor in hormonal biosynthesis, but through an alternative pathway. This constitutes an exception in the animal kingdom.
Experiments with Fetal Horse Gonads
- The investigators conducted experiments with fetal horse gonads by incubating them with tritiated sodium acetate, which is a type of isotope-labelled sodium acetate for tracing chemical reactions.
- A result of this experiment was the detection of two chemically pure hormones, namely 3 beta-hydroxy-5,7-pregnadien-20-one and 3 beta-hydroxy-5,7-androstadien-17-one. These two hormones play a crucial role in the unique biosynthesis pathway.
Fetal Gonad-Placental System For Hormone Production
- The research paper suggests a two-step hormonal production system in pregnant mares, where the progestogen hormone 3 beta-hydroxy-5,7-pregnadien-20-one is produced in the fetal gonad.
- This hormone then serves as precursor for the production of androgenic hormone 3 beta-hydroxy-5,7-androstadien-17-one, also in the fetal gonad.
- 3 beta-hydroxy-5,7-androstadien-17-one further serves as precursor of equilin, an estrogen, in the placenta of the pregnant mare.
Potential Precursor of 3 beta-hydroxy-5,7-pregnadien-20-one
- While the paper outlines this special biosynthesis pathway, it also raises discussion about what could be the possible precursor of 3 beta-hydroxy-5,7-pregnadien-20-one. This opens up new avenues of investigation to fully understand this unique and rare biosynthesis pathway in horses.
Cite This Article
APA
Tait AD, Hodge LC, Allen WR.
(1983).
Biosynthesis of 3 beta-hydroxy-5,7-pregnadien-20-one by the horse fetal gonad.
FEBS Lett, 153(1), 161-164.
https://doi.org/10.1016/0014-5793(83)80139-2 Publication
Researcher Affiliations
MeSH Terms
- Animals
- Dehydroepiandrosterone / metabolism
- Equilin / biosynthesis
- Gonads / embryology
- Gonads / metabolism
- Horses / embryology
- In Vitro Techniques
- Pregnadienes / biosynthesis
- Pregnenolone / metabolism
Citations
This article has been cited 5 times.- Slominski AT, Li W, Kim TK, Semak I, Wang J, Zjawiony JK, Tuckey RC. Novel activities of CYP11A1 and their potential physiological significance.. J Steroid Biochem Mol Biol 2015 Jul;151:25-37.
- Slominski AT, Kim TK, Chen J, Nguyen MN, Li W, Yates CR, Sweatman T, Janjetovic Z, Tuckey RC. Cytochrome P450scc-dependent metabolism of 7-dehydrocholesterol in placenta and epidermal keratinocytes.. Int J Biochem Cell Biol 2012 Nov;44(11):2003-18.
- Zmijewski MA, Li W, Chen J, Kim TK, Zjawiony JK, Sweatman TW, Miller DD, Slominski AT. Synthesis and photochemical transformation of 3β,21-dihydroxypregna-5,7-dien-20-one to novel secosteroids that show anti-melanoma activity.. Steroids 2011 Jan;76(1-2):193-203.
- Zmijewski MA, Li W, Zjawiony JK, Sweatman TW, Chen J, Miller DD, Slominski AT. Synthesis and photo-conversion of androsta- and pregna-5,7-dienes to vitamin D3-like derivatives.. Photochem Photobiol Sci 2008 Dec;7(12):1570-6.
- Zmijewski MA, Li W, Zjawiony JK, Sweatman TW, Chen J, Miller DD, Slominski AT. Photo-conversion of two epimers (20R and 20S) of pregna-5,7-diene-3beta, 17alpha, 20-triol and their bioactivity in melanoma cells.. Steroids 2009 Feb;74(2):218-28.
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