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Impact of Oxidative Stress on Age-Associated Decline in Oocyte Developmental Competence
Reproductive capacity in women starts to decline beyond their mid-30s and pregnancies in older women result in higher rates of miscarriage with aneuploidy. Age-related decline in fertility is strongly attributed to ovarian aging, diminished ovarian reserves, and decreased developmental competence of...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6882737/ https://www.ncbi.nlm.nih.gov/pubmed/31824426 http://dx.doi.org/10.3389/fendo.2019.00811 |
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author | Sasaki, Hiroyuki Hamatani, Toshio Kamijo, Shintaro Iwai, Maki Kobanawa, Masato Ogawa, Seiji Miyado, Kenji Tanaka, Mamoru |
author_facet | Sasaki, Hiroyuki Hamatani, Toshio Kamijo, Shintaro Iwai, Maki Kobanawa, Masato Ogawa, Seiji Miyado, Kenji Tanaka, Mamoru |
author_sort | Sasaki, Hiroyuki |
collection | PubMed |
description | Reproductive capacity in women starts to decline beyond their mid-30s and pregnancies in older women result in higher rates of miscarriage with aneuploidy. Age-related decline in fertility is strongly attributed to ovarian aging, diminished ovarian reserves, and decreased developmental competence of oocytes. In this review, we discuss the underlying mechanisms of age-related decline in oocyte quality, focusing on oxidative stress (OS) in oocytes. The primary cause is the accumulation of spontaneous damage to the mitochondria arising from increased reactive oxygen species (ROS) in oocytes, generated by the mitochondria themselves during daily biological metabolism. Mitochondrial dysfunction reduces ATP synthesis and influences the meiotic spindle assembly responsible for chromosomal segregation. Moreover, reproductively aged oocytes produce a decline in the fidelity of the protective mechanisms against ROS, namely the ROS-scavenging metabolism, repair of ROS-damaged DNA, and the proteasome and autophagy system for ROS-damaged proteins. Accordingly, increased ROS and increased vulnerability of oocytes to ROS lead to spindle instability, chromosomal abnormalities, telomere shortening, and reduced developmental competence of aged oocytes. |
format | Online Article Text |
id | pubmed-6882737 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68827372019-12-10 Impact of Oxidative Stress on Age-Associated Decline in Oocyte Developmental Competence Sasaki, Hiroyuki Hamatani, Toshio Kamijo, Shintaro Iwai, Maki Kobanawa, Masato Ogawa, Seiji Miyado, Kenji Tanaka, Mamoru Front Endocrinol (Lausanne) Endocrinology Reproductive capacity in women starts to decline beyond their mid-30s and pregnancies in older women result in higher rates of miscarriage with aneuploidy. Age-related decline in fertility is strongly attributed to ovarian aging, diminished ovarian reserves, and decreased developmental competence of oocytes. In this review, we discuss the underlying mechanisms of age-related decline in oocyte quality, focusing on oxidative stress (OS) in oocytes. The primary cause is the accumulation of spontaneous damage to the mitochondria arising from increased reactive oxygen species (ROS) in oocytes, generated by the mitochondria themselves during daily biological metabolism. Mitochondrial dysfunction reduces ATP synthesis and influences the meiotic spindle assembly responsible for chromosomal segregation. Moreover, reproductively aged oocytes produce a decline in the fidelity of the protective mechanisms against ROS, namely the ROS-scavenging metabolism, repair of ROS-damaged DNA, and the proteasome and autophagy system for ROS-damaged proteins. Accordingly, increased ROS and increased vulnerability of oocytes to ROS lead to spindle instability, chromosomal abnormalities, telomere shortening, and reduced developmental competence of aged oocytes. Frontiers Media S.A. 2019-11-22 /pmc/articles/PMC6882737/ /pubmed/31824426 http://dx.doi.org/10.3389/fendo.2019.00811 Text en Copyright © 2019 Sasaki, Hamatani, Kamijo, Iwai, Kobanawa, Ogawa, Miyado and Tanaka. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Endocrinology Sasaki, Hiroyuki Hamatani, Toshio Kamijo, Shintaro Iwai, Maki Kobanawa, Masato Ogawa, Seiji Miyado, Kenji Tanaka, Mamoru Impact of Oxidative Stress on Age-Associated Decline in Oocyte Developmental Competence |
title | Impact of Oxidative Stress on Age-Associated Decline in Oocyte Developmental Competence |
title_full | Impact of Oxidative Stress on Age-Associated Decline in Oocyte Developmental Competence |
title_fullStr | Impact of Oxidative Stress on Age-Associated Decline in Oocyte Developmental Competence |
title_full_unstemmed | Impact of Oxidative Stress on Age-Associated Decline in Oocyte Developmental Competence |
title_short | Impact of Oxidative Stress on Age-Associated Decline in Oocyte Developmental Competence |
title_sort | impact of oxidative stress on age-associated decline in oocyte developmental competence |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6882737/ https://www.ncbi.nlm.nih.gov/pubmed/31824426 http://dx.doi.org/10.3389/fendo.2019.00811 |
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