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Relationship between Advanced Glycation End Products and Steroidogenesis in PCOS

BACKGROUND: Women with PCOS have elevated levels of the harmful Advanced Glycation End Products (AGEs), which are highly reactive molecules formed after glycation of lipids and proteins. Additionally, AGEs accumulate in the ovaries of women with PCOS potentially contributing to the well-documented a...

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Autores principales: Garg, Deepika, Merhi, Zaher
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5073880/
https://www.ncbi.nlm.nih.gov/pubmed/27769286
http://dx.doi.org/10.1186/s12958-016-0205-6
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author Garg, Deepika
Merhi, Zaher
author_facet Garg, Deepika
Merhi, Zaher
author_sort Garg, Deepika
collection PubMed
description BACKGROUND: Women with PCOS have elevated levels of the harmful Advanced Glycation End Products (AGEs), which are highly reactive molecules formed after glycation of lipids and proteins. Additionally, AGEs accumulate in the ovaries of women with PCOS potentially contributing to the well-documented abnormal steroidogenesis and folliculogenesis. MAIN BODY: A systematic review of articles and abstracts available in PubMed was conducted and presented in a systemic manner. This article reports changes in steroidogenic enzyme activity in granulosa and theca cells in PCOS and PCOS-models. It also described the changes in AGEs and their receptors in the ovaries of women with PCOS and presents the underlying mechanism(s) whereby AGEs could be responsible for the PCOS-related changes in granulosa and theca cell function thus adversely impacting steroidogenesis and follicular development. AGEs are associated with hyperandrogenism in PCOS possibly by altering the activity of various enzymes such as cholesterol side-chain cleavage enzyme cytochrome P450, steroidogenic acute regulatory protein, 17α-hydroxylase, and 3β-hydroxysteroid dehydrogenase. AGEs also affect luteinizing hormone receptor and anti-Mullerian hormone receptor expression as well as their signaling pathways in granulosa cells. CONCLUSIONS: A better understanding of how AGEs alter granulosa and theca cell function is likely to contribute meaningfully to a conceptual framework whereby new interventions to prevent and/or treat ovarian dysfunction in PCOS can ultimately be developed.
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spelling pubmed-50738802016-10-26 Relationship between Advanced Glycation End Products and Steroidogenesis in PCOS Garg, Deepika Merhi, Zaher Reprod Biol Endocrinol Review BACKGROUND: Women with PCOS have elevated levels of the harmful Advanced Glycation End Products (AGEs), which are highly reactive molecules formed after glycation of lipids and proteins. Additionally, AGEs accumulate in the ovaries of women with PCOS potentially contributing to the well-documented abnormal steroidogenesis and folliculogenesis. MAIN BODY: A systematic review of articles and abstracts available in PubMed was conducted and presented in a systemic manner. This article reports changes in steroidogenic enzyme activity in granulosa and theca cells in PCOS and PCOS-models. It also described the changes in AGEs and their receptors in the ovaries of women with PCOS and presents the underlying mechanism(s) whereby AGEs could be responsible for the PCOS-related changes in granulosa and theca cell function thus adversely impacting steroidogenesis and follicular development. AGEs are associated with hyperandrogenism in PCOS possibly by altering the activity of various enzymes such as cholesterol side-chain cleavage enzyme cytochrome P450, steroidogenic acute regulatory protein, 17α-hydroxylase, and 3β-hydroxysteroid dehydrogenase. AGEs also affect luteinizing hormone receptor and anti-Mullerian hormone receptor expression as well as their signaling pathways in granulosa cells. CONCLUSIONS: A better understanding of how AGEs alter granulosa and theca cell function is likely to contribute meaningfully to a conceptual framework whereby new interventions to prevent and/or treat ovarian dysfunction in PCOS can ultimately be developed. BioMed Central 2016-10-21 /pmc/articles/PMC5073880/ /pubmed/27769286 http://dx.doi.org/10.1186/s12958-016-0205-6 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Garg, Deepika
Merhi, Zaher
Relationship between Advanced Glycation End Products and Steroidogenesis in PCOS
title Relationship between Advanced Glycation End Products and Steroidogenesis in PCOS
title_full Relationship between Advanced Glycation End Products and Steroidogenesis in PCOS
title_fullStr Relationship between Advanced Glycation End Products and Steroidogenesis in PCOS
title_full_unstemmed Relationship between Advanced Glycation End Products and Steroidogenesis in PCOS
title_short Relationship between Advanced Glycation End Products and Steroidogenesis in PCOS
title_sort relationship between advanced glycation end products and steroidogenesis in pcos
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5073880/
https://www.ncbi.nlm.nih.gov/pubmed/27769286
http://dx.doi.org/10.1186/s12958-016-0205-6
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