Harvard
Savchuk, I, Morvan, M-L
, Søeborg, T, Antignac, J-P, Gemzell-Danielsson, K, Bizec, BL, Söder, O & Svechnikov, K 2017, '
Resveratrol inhibits steroidogenesis in human fetal adrenocortical cells at the end of first trimester',
Molecular Nutrition & Food Research, bind 61, nr. 2, s. 1600522.
https://doi.org/10.1002/mnfr.201600522
APA
Savchuk, I., Morvan, M-L.
, Søeborg, T., Antignac, J-P., Gemzell-Danielsson, K., Bizec, B. L., Söder, O., & Svechnikov, K. (2017).
Resveratrol inhibits steroidogenesis in human fetal adrenocortical cells at the end of first trimester.
Molecular Nutrition & Food Research,
61(2), 1600522.
https://doi.org/10.1002/mnfr.201600522
CBE
MLA
Vancouver
Author
Bibtex
@article{bcaccf35b0e345b3b95fdc0d761de8fa,
title = "Resveratrol inhibits steroidogenesis in human fetal adrenocortical cells at the end of first trimester",
abstract = "SCOPE: Resveratrol has a diverse array of healthful effects on metabolic parameters in different experimental paradigms but has also potential to inhibit steroidogenesis in rodent adrenals. The aim of the present study was to characterize the effects of resveratrol on human fetal adrenal steroidogenesis at gestational weeks (GW) 9-12.METHODS AND RESULTS: Adrenals from aborted fetuses (GW10-12) were used to prepare primary cultures of human fetal adrenocortical cells (HFAC). HFAC were treated in the presence or absence of ACTH (10 ng/ml) with or without resveratrol (10 μM) for 24 hours. The production of steroids by HFAC was analyzed by gas and liquid chromatography coupled to tandem/mass spectrometry. The expression of steroidogenic enzymes at GW 9-12 was quantified by automated Western blotting. We observed that resveratrol significantly suppressed synthesis of dehydroepiandrosterone (DHEA), androstenedione and 11-deoxicortisol by ACTH-activated and unstimulated HFAC, which was associated with inhibition of the activities and expression of cytochromes 17α-hydroxylase/17,20 lyase (CYP17) and 21-hydroxylase (CYP21) in these fetal adrenocortical cells.CONCLUSION: Our in vitro findings on the sensitivity of human fetal adrenal steroidogenesis to resveratrol at GW9-12 suggest that intake of this polyphenol at high doses by women who are at early stages of pregnancy is undesirable. This article is protected by copyright. All rights reserved.",
author = "Iuliia Savchuk and Marie-Line Morvan and Tue S{\o}eborg and Jean-Philippe Antignac and Kristina Gemzell-Danielsson and Bizec, {Bruno Le} and Olle S{\"o}der and Konstantin Svechnikov",
note = "This article is protected by copyright. All rights reserved.",
year = "2017",
doi = "10.1002/mnfr.201600522",
language = "English",
volume = "61",
pages = "1600522",
journal = "Molecular Nutrition & Food Research",
issn = "1613-4125",
publisher = "Wiley - V C H Verlag GmbH & Co. KGaA",
number = "2",
}
RIS
TY - JOUR
T1 - Resveratrol inhibits steroidogenesis in human fetal adrenocortical cells at the end of first trimester
AU - Savchuk, Iuliia
AU - Morvan, Marie-Line
AU - Søeborg, Tue
AU - Antignac, Jean-Philippe
AU - Gemzell-Danielsson, Kristina
AU - Bizec, Bruno Le
AU - Söder, Olle
AU - Svechnikov, Konstantin
N1 - This article is protected by copyright. All rights reserved.
PY - 2017
Y1 - 2017
N2 - SCOPE: Resveratrol has a diverse array of healthful effects on metabolic parameters in different experimental paradigms but has also potential to inhibit steroidogenesis in rodent adrenals. The aim of the present study was to characterize the effects of resveratrol on human fetal adrenal steroidogenesis at gestational weeks (GW) 9-12.METHODS AND RESULTS: Adrenals from aborted fetuses (GW10-12) were used to prepare primary cultures of human fetal adrenocortical cells (HFAC). HFAC were treated in the presence or absence of ACTH (10 ng/ml) with or without resveratrol (10 μM) for 24 hours. The production of steroids by HFAC was analyzed by gas and liquid chromatography coupled to tandem/mass spectrometry. The expression of steroidogenic enzymes at GW 9-12 was quantified by automated Western blotting. We observed that resveratrol significantly suppressed synthesis of dehydroepiandrosterone (DHEA), androstenedione and 11-deoxicortisol by ACTH-activated and unstimulated HFAC, which was associated with inhibition of the activities and expression of cytochromes 17α-hydroxylase/17,20 lyase (CYP17) and 21-hydroxylase (CYP21) in these fetal adrenocortical cells.CONCLUSION: Our in vitro findings on the sensitivity of human fetal adrenal steroidogenesis to resveratrol at GW9-12 suggest that intake of this polyphenol at high doses by women who are at early stages of pregnancy is undesirable. This article is protected by copyright. All rights reserved.
AB - SCOPE: Resveratrol has a diverse array of healthful effects on metabolic parameters in different experimental paradigms but has also potential to inhibit steroidogenesis in rodent adrenals. The aim of the present study was to characterize the effects of resveratrol on human fetal adrenal steroidogenesis at gestational weeks (GW) 9-12.METHODS AND RESULTS: Adrenals from aborted fetuses (GW10-12) were used to prepare primary cultures of human fetal adrenocortical cells (HFAC). HFAC were treated in the presence or absence of ACTH (10 ng/ml) with or without resveratrol (10 μM) for 24 hours. The production of steroids by HFAC was analyzed by gas and liquid chromatography coupled to tandem/mass spectrometry. The expression of steroidogenic enzymes at GW 9-12 was quantified by automated Western blotting. We observed that resveratrol significantly suppressed synthesis of dehydroepiandrosterone (DHEA), androstenedione and 11-deoxicortisol by ACTH-activated and unstimulated HFAC, which was associated with inhibition of the activities and expression of cytochromes 17α-hydroxylase/17,20 lyase (CYP17) and 21-hydroxylase (CYP21) in these fetal adrenocortical cells.CONCLUSION: Our in vitro findings on the sensitivity of human fetal adrenal steroidogenesis to resveratrol at GW9-12 suggest that intake of this polyphenol at high doses by women who are at early stages of pregnancy is undesirable. This article is protected by copyright. All rights reserved.
U2 - 10.1002/mnfr.201600522
DO - 10.1002/mnfr.201600522
M3 - Journal article
C2 - 27561679
VL - 61
SP - 1600522
JO - Molecular Nutrition & Food Research
JF - Molecular Nutrition & Food Research
SN - 1613-4125
IS - 2
ER -