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3-Nitropropionic Acid Induces Ovarian Oxidative Stress and Impairs Follicle in Mouse

Oxidative stress induces many serious reproductive diseases in female mammals and thus poses a serious threat to reproductive health. However, the relationship between reactive oxygen species (ROS)—induced oxidative stress and follicular development, oocyte and embryo quality is not clear. The aim o...

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Autores principales: Zhang, Jia-Qing, Shen, Ming, Zhu, Cheng-Cheng, Yu, Feng-Xiang, Liu, Ze-Qun, Ally, Nazim, Sun, Shao-Chen, Li, Kui, Liu, Hong-Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3914797/
https://www.ncbi.nlm.nih.gov/pubmed/24505260
http://dx.doi.org/10.1371/journal.pone.0086589
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author Zhang, Jia-Qing
Shen, Ming
Zhu, Cheng-Cheng
Yu, Feng-Xiang
Liu, Ze-Qun
Ally, Nazim
Sun, Shao-Chen
Li, Kui
Liu, Hong-Lin
author_facet Zhang, Jia-Qing
Shen, Ming
Zhu, Cheng-Cheng
Yu, Feng-Xiang
Liu, Ze-Qun
Ally, Nazim
Sun, Shao-Chen
Li, Kui
Liu, Hong-Lin
author_sort Zhang, Jia-Qing
collection PubMed
description Oxidative stress induces many serious reproductive diseases in female mammals and thus poses a serious threat to reproductive health. However, the relationship between reactive oxygen species (ROS)—induced oxidative stress and follicular development, oocyte and embryo quality is not clear. The aim of this study was to investigate the effect of ovarian oxidative stress on the health of follicle and oocyte development. Female ICR mice were dosed with 3-nitropropionic acid (3-NPA) at three different concentrations (6.25, 12.5 and 25 mg/kg) and saline (control) via continuous intraperitoneal injection for 7 days. The treatment with 12.5 mg/kg reduced the weight of mouse ovaries, and significantly increased ROS levels and the activities of antioxidant enzymes—total superoxide dismutase (T-SOD), glutathione peroxidase (GPx) and catalase (CAT) — in granulosa cells and ovarian tissues, but not in other tissues (brain, liver, kidney and spleen). The same treatment significantly increased the percentage of atretic large follicles, and reduced the number of large follicles, the number of ovulated oocytes, and the capacity for early embryonic development compared with controls. It also significantly decreased the ratio of Bcl-2 to Bax, while causing an increase in the mRNA expression of (SOD2, CAT and GP (X)) and ROS levels in granulosa cells. Collectively, these data indicate that 3-NPA induces granulosa cell apoptosis, large follicle atresia, and an increase of ROS levels in the ovary. Therefore, we have established an in vivo model of ovarian oxidative stress for studying the mechanism of resulting damage induced by free radicals and for the screening of novel antioxidants.
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spelling pubmed-39147972014-02-06 3-Nitropropionic Acid Induces Ovarian Oxidative Stress and Impairs Follicle in Mouse Zhang, Jia-Qing Shen, Ming Zhu, Cheng-Cheng Yu, Feng-Xiang Liu, Ze-Qun Ally, Nazim Sun, Shao-Chen Li, Kui Liu, Hong-Lin PLoS One Research Article Oxidative stress induces many serious reproductive diseases in female mammals and thus poses a serious threat to reproductive health. However, the relationship between reactive oxygen species (ROS)—induced oxidative stress and follicular development, oocyte and embryo quality is not clear. The aim of this study was to investigate the effect of ovarian oxidative stress on the health of follicle and oocyte development. Female ICR mice were dosed with 3-nitropropionic acid (3-NPA) at three different concentrations (6.25, 12.5 and 25 mg/kg) and saline (control) via continuous intraperitoneal injection for 7 days. The treatment with 12.5 mg/kg reduced the weight of mouse ovaries, and significantly increased ROS levels and the activities of antioxidant enzymes—total superoxide dismutase (T-SOD), glutathione peroxidase (GPx) and catalase (CAT) — in granulosa cells and ovarian tissues, but not in other tissues (brain, liver, kidney and spleen). The same treatment significantly increased the percentage of atretic large follicles, and reduced the number of large follicles, the number of ovulated oocytes, and the capacity for early embryonic development compared with controls. It also significantly decreased the ratio of Bcl-2 to Bax, while causing an increase in the mRNA expression of (SOD2, CAT and GP (X)) and ROS levels in granulosa cells. Collectively, these data indicate that 3-NPA induces granulosa cell apoptosis, large follicle atresia, and an increase of ROS levels in the ovary. Therefore, we have established an in vivo model of ovarian oxidative stress for studying the mechanism of resulting damage induced by free radicals and for the screening of novel antioxidants. Public Library of Science 2014-02-05 /pmc/articles/PMC3914797/ /pubmed/24505260 http://dx.doi.org/10.1371/journal.pone.0086589 Text en © 2014 Zhang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Zhang, Jia-Qing
Shen, Ming
Zhu, Cheng-Cheng
Yu, Feng-Xiang
Liu, Ze-Qun
Ally, Nazim
Sun, Shao-Chen
Li, Kui
Liu, Hong-Lin
3-Nitropropionic Acid Induces Ovarian Oxidative Stress and Impairs Follicle in Mouse
title 3-Nitropropionic Acid Induces Ovarian Oxidative Stress and Impairs Follicle in Mouse
title_full 3-Nitropropionic Acid Induces Ovarian Oxidative Stress and Impairs Follicle in Mouse
title_fullStr 3-Nitropropionic Acid Induces Ovarian Oxidative Stress and Impairs Follicle in Mouse
title_full_unstemmed 3-Nitropropionic Acid Induces Ovarian Oxidative Stress and Impairs Follicle in Mouse
title_short 3-Nitropropionic Acid Induces Ovarian Oxidative Stress and Impairs Follicle in Mouse
title_sort 3-nitropropionic acid induces ovarian oxidative stress and impairs follicle in mouse
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3914797/
https://www.ncbi.nlm.nih.gov/pubmed/24505260
http://dx.doi.org/10.1371/journal.pone.0086589
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