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The Effect of Oxidative Stress on the Chicken Ovary: Involvement of Microbiota and Melatonin Interventions

The poultry ovary is used as a classic model to study ovarian biology and ovarian cancer. Stress factors induced oxidative stress to cause follicle atresia, which may be a fundamental reason for the reduction in fertility in older laying hens or in aging women. In the present study, we set out to ch...

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Autores principales: Wang, Jianping, Jia, Ru, Gong, Haojie, Celi, Pietro, Zhuo, Yong, Ding, Xuemei, Bai, Shiping, Zeng, Qiufeng, Yin, Huadong, Xu, Shengyu, Liu, Jingbo, Mao, Xiangbing, Zhang, Keying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8472688/
https://www.ncbi.nlm.nih.gov/pubmed/34573054
http://dx.doi.org/10.3390/antiox10091422
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author Wang, Jianping
Jia, Ru
Gong, Haojie
Celi, Pietro
Zhuo, Yong
Ding, Xuemei
Bai, Shiping
Zeng, Qiufeng
Yin, Huadong
Xu, Shengyu
Liu, Jingbo
Mao, Xiangbing
Zhang, Keying
author_facet Wang, Jianping
Jia, Ru
Gong, Haojie
Celi, Pietro
Zhuo, Yong
Ding, Xuemei
Bai, Shiping
Zeng, Qiufeng
Yin, Huadong
Xu, Shengyu
Liu, Jingbo
Mao, Xiangbing
Zhang, Keying
author_sort Wang, Jianping
collection PubMed
description The poultry ovary is used as a classic model to study ovarian biology and ovarian cancer. Stress factors induced oxidative stress to cause follicle atresia, which may be a fundamental reason for the reduction in fertility in older laying hens or in aging women. In the present study, we set out to characterize the relationships between oxidative stress and ovarian function. Layers (62 weeks of age; BW = 1.42 ± 0.12 kg) were injected with tert-butyl hydroperoxide (tBHP) at 0 (CON) and 800 μmol/kg BW (oxidative stress group, OS) for 24 days and the role of melatonin (Mel) on tBHP-induced ovary oxidative stress was assessed through ovary culture in vitro. The OS (800 μmol/kg BW tert-butyl hydroperoxide) treatment decreased the reproduction performance and ovarian follicle numbers. OS decreased the expression of SIRT1 and increased the P53 and FoxO1 expression of the ovary. A decreased Firmicutes to Bacteroidetes ratio, enriched Marinifilaceae (family), Odoribacter (genus) and Bacteroides_plebeius (species) were observed in the cecum of the OS group. Using Mel in vitro enhanced the follicle numbers and decreased the ovary cell apoptosis induced by tBHP. In addition, it increased the expression of SIRT1 and decreased the P53 and FoxO1 expression. These findings indicated that oxidative stress could decrease the laying performance, ovarian function and influence gut microbiota and body metabolites in the layer model, while the melatonin exerts an amelioration the ovary oxidative stress through SIRT1-P53/FoxO1 pathway.
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spelling pubmed-84726882021-09-28 The Effect of Oxidative Stress on the Chicken Ovary: Involvement of Microbiota and Melatonin Interventions Wang, Jianping Jia, Ru Gong, Haojie Celi, Pietro Zhuo, Yong Ding, Xuemei Bai, Shiping Zeng, Qiufeng Yin, Huadong Xu, Shengyu Liu, Jingbo Mao, Xiangbing Zhang, Keying Antioxidants (Basel) Article The poultry ovary is used as a classic model to study ovarian biology and ovarian cancer. Stress factors induced oxidative stress to cause follicle atresia, which may be a fundamental reason for the reduction in fertility in older laying hens or in aging women. In the present study, we set out to characterize the relationships between oxidative stress and ovarian function. Layers (62 weeks of age; BW = 1.42 ± 0.12 kg) were injected with tert-butyl hydroperoxide (tBHP) at 0 (CON) and 800 μmol/kg BW (oxidative stress group, OS) for 24 days and the role of melatonin (Mel) on tBHP-induced ovary oxidative stress was assessed through ovary culture in vitro. The OS (800 μmol/kg BW tert-butyl hydroperoxide) treatment decreased the reproduction performance and ovarian follicle numbers. OS decreased the expression of SIRT1 and increased the P53 and FoxO1 expression of the ovary. A decreased Firmicutes to Bacteroidetes ratio, enriched Marinifilaceae (family), Odoribacter (genus) and Bacteroides_plebeius (species) were observed in the cecum of the OS group. Using Mel in vitro enhanced the follicle numbers and decreased the ovary cell apoptosis induced by tBHP. In addition, it increased the expression of SIRT1 and decreased the P53 and FoxO1 expression. These findings indicated that oxidative stress could decrease the laying performance, ovarian function and influence gut microbiota and body metabolites in the layer model, while the melatonin exerts an amelioration the ovary oxidative stress through SIRT1-P53/FoxO1 pathway. MDPI 2021-09-06 /pmc/articles/PMC8472688/ /pubmed/34573054 http://dx.doi.org/10.3390/antiox10091422 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wang, Jianping
Jia, Ru
Gong, Haojie
Celi, Pietro
Zhuo, Yong
Ding, Xuemei
Bai, Shiping
Zeng, Qiufeng
Yin, Huadong
Xu, Shengyu
Liu, Jingbo
Mao, Xiangbing
Zhang, Keying
The Effect of Oxidative Stress on the Chicken Ovary: Involvement of Microbiota and Melatonin Interventions
title The Effect of Oxidative Stress on the Chicken Ovary: Involvement of Microbiota and Melatonin Interventions
title_full The Effect of Oxidative Stress on the Chicken Ovary: Involvement of Microbiota and Melatonin Interventions
title_fullStr The Effect of Oxidative Stress on the Chicken Ovary: Involvement of Microbiota and Melatonin Interventions
title_full_unstemmed The Effect of Oxidative Stress on the Chicken Ovary: Involvement of Microbiota and Melatonin Interventions
title_short The Effect of Oxidative Stress on the Chicken Ovary: Involvement of Microbiota and Melatonin Interventions
title_sort effect of oxidative stress on the chicken ovary: involvement of microbiota and melatonin interventions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8472688/
https://www.ncbi.nlm.nih.gov/pubmed/34573054
http://dx.doi.org/10.3390/antiox10091422
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