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Corticosterone metabolism by chicken follicle cells does not affect ovarian reproductive hormone synthesis in vitro

Glucocorticoids affect reproductive hormone production in many species. In chickens, elevated plasma corticosterone down-regulates testosterone and progesterone concentrations in plasma, but also in egg yolk. This suppression could be mediated via the hypothalamic-pituitary system but also via local...

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Autores principales: Rettenbacher, Sophie, Henriksen, Rie, Groothuids, Ton G., Lepschy, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3601324/
https://www.ncbi.nlm.nih.gov/pubmed/23333751
http://dx.doi.org/10.1016/j.ygcen.2012.12.013
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author Rettenbacher, Sophie
Henriksen, Rie
Groothuids, Ton G.
Lepschy, Michael
author_facet Rettenbacher, Sophie
Henriksen, Rie
Groothuids, Ton G.
Lepschy, Michael
author_sort Rettenbacher, Sophie
collection PubMed
description Glucocorticoids affect reproductive hormone production in many species. In chickens, elevated plasma corticosterone down-regulates testosterone and progesterone concentrations in plasma, but also in egg yolk. This suppression could be mediated via the hypothalamic-pituitary system but also via local inhibition of gonadal activity by glucocorticoids. As the latter has not been tested in birds yet, we tested if corticosterone directly inhibits ovarian steroid synthesis under in vitro conditions. We hypothesized that degradation of corticosterone by follicular cells impairs their ability to synthesize reproductive hormones due to either inhibition of enzymes or competition for common co-factors. Therefore, we first established whether follicles degrade corticosterone. Follicular tissue was harvested from freshly euthanized laying hens and incubated with radiolabelled corticosterone. Radioactive metabolites were visualized and quantified by autoradiography. Follicles converted corticosterone in a time-dependent manner into metabolites with a higher polarity than corticosterone. The predominant metabolite co-eluted with 20β-dihydrocorticosterone. Other chicken tissues mostly formed the same metabolite when incubated with corticosterone. In a second experiment, follicles were incubated with either progesterone or dehydroepiandrosterone. Corticosterone was added in increasing dosages up to 1000 ng per ml medium. Corticosterone did not inhibit the conversion of progesterone and dehydroepiandrosterone into a number of different metabolites, including 17α-hydroxyprogesterone, androstenedione and testosterone. In conclusion, avian tissues degrade corticosterone mostly to 20β-dihydrocorticosterone and even high corticosterone dosages do not affect follicular hormone production under in vitro conditions.
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spelling pubmed-36013242013-04-01 Corticosterone metabolism by chicken follicle cells does not affect ovarian reproductive hormone synthesis in vitro Rettenbacher, Sophie Henriksen, Rie Groothuids, Ton G. Lepschy, Michael Gen Comp Endocrinol Article Glucocorticoids affect reproductive hormone production in many species. In chickens, elevated plasma corticosterone down-regulates testosterone and progesterone concentrations in plasma, but also in egg yolk. This suppression could be mediated via the hypothalamic-pituitary system but also via local inhibition of gonadal activity by glucocorticoids. As the latter has not been tested in birds yet, we tested if corticosterone directly inhibits ovarian steroid synthesis under in vitro conditions. We hypothesized that degradation of corticosterone by follicular cells impairs their ability to synthesize reproductive hormones due to either inhibition of enzymes or competition for common co-factors. Therefore, we first established whether follicles degrade corticosterone. Follicular tissue was harvested from freshly euthanized laying hens and incubated with radiolabelled corticosterone. Radioactive metabolites were visualized and quantified by autoradiography. Follicles converted corticosterone in a time-dependent manner into metabolites with a higher polarity than corticosterone. The predominant metabolite co-eluted with 20β-dihydrocorticosterone. Other chicken tissues mostly formed the same metabolite when incubated with corticosterone. In a second experiment, follicles were incubated with either progesterone or dehydroepiandrosterone. Corticosterone was added in increasing dosages up to 1000 ng per ml medium. Corticosterone did not inhibit the conversion of progesterone and dehydroepiandrosterone into a number of different metabolites, including 17α-hydroxyprogesterone, androstenedione and testosterone. In conclusion, avian tissues degrade corticosterone mostly to 20β-dihydrocorticosterone and even high corticosterone dosages do not affect follicular hormone production under in vitro conditions. Academic Press 2013-04-01 /pmc/articles/PMC3601324/ /pubmed/23333751 http://dx.doi.org/10.1016/j.ygcen.2012.12.013 Text en © 2013 Elsevier Inc. https://creativecommons.org/licenses/by-nc-nd/3.0/ Open Access under CC BY-NC-ND 3.0 (https://creativecommons.org/licenses/by-nc-nd/3.0/) license
spellingShingle Article
Rettenbacher, Sophie
Henriksen, Rie
Groothuids, Ton G.
Lepschy, Michael
Corticosterone metabolism by chicken follicle cells does not affect ovarian reproductive hormone synthesis in vitro
title Corticosterone metabolism by chicken follicle cells does not affect ovarian reproductive hormone synthesis in vitro
title_full Corticosterone metabolism by chicken follicle cells does not affect ovarian reproductive hormone synthesis in vitro
title_fullStr Corticosterone metabolism by chicken follicle cells does not affect ovarian reproductive hormone synthesis in vitro
title_full_unstemmed Corticosterone metabolism by chicken follicle cells does not affect ovarian reproductive hormone synthesis in vitro
title_short Corticosterone metabolism by chicken follicle cells does not affect ovarian reproductive hormone synthesis in vitro
title_sort corticosterone metabolism by chicken follicle cells does not affect ovarian reproductive hormone synthesis in vitro
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3601324/
https://www.ncbi.nlm.nih.gov/pubmed/23333751
http://dx.doi.org/10.1016/j.ygcen.2012.12.013
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