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Inhibitory effects of astaxanthin on postovulatory porcine oocyte aging in vitro
Mammalian oocytes represent impaired quality after undergoing a process of postovulatory aging, which can be alleviated through various effective ways such as reagent treatment. Accumulating evidences have revealed the beneficial effects of astaxanthin (Ax) as a potential antioxidant on reproductive...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7677382/ https://www.ncbi.nlm.nih.gov/pubmed/33214659 http://dx.doi.org/10.1038/s41598-020-77359-6 |
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author | Jia, Bao-Yu Xiang, De-Cai Shao, Qing-Yong Zhang, Bin Liu, Shao-Na Hong, Qiong-Hua Quan, Guo-Bo Wu, Guo-Quan |
author_facet | Jia, Bao-Yu Xiang, De-Cai Shao, Qing-Yong Zhang, Bin Liu, Shao-Na Hong, Qiong-Hua Quan, Guo-Bo Wu, Guo-Quan |
author_sort | Jia, Bao-Yu |
collection | PubMed |
description | Mammalian oocytes represent impaired quality after undergoing a process of postovulatory aging, which can be alleviated through various effective ways such as reagent treatment. Accumulating evidences have revealed the beneficial effects of astaxanthin (Ax) as a potential antioxidant on reproductive biology. Here, porcine matured oocytes were used as a model to explore whether Ax supplement can protect against oocyte aging in vitro and the underlying mechanism, and therefore they were cultured with or without 2.5 μM Ax for an additional 24 h. Aged oocytes treated with Ax showed improved yield and quality of blastocysts as well as recovered expression of maternal genes. Importantly, oxidative stress in aged oocytes was relieved through Ax treatment, based on reduced reactive oxygen species and enhanced glutathione and antioxidant gene expression. Moreover, inhibition in apoptosis and autophagy of aged oocyte by Ax was confirmed through decreased caspase-3, cathepsin B and autophagic activities. Ax could also maintain spindle organization and actin expression, and rescue functional status of organelles including mitochondria, endoplasmic reticulum, Golgi apparatus and lysosomes according to restored fluorescence intensity. In conclusion, Ax might provide an alternative for ameliorating the oocyte quality following aging in vitro, through the mechanisms mediated by its antioxidant properties. |
format | Online Article Text |
id | pubmed-7677382 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-76773822020-11-23 Inhibitory effects of astaxanthin on postovulatory porcine oocyte aging in vitro Jia, Bao-Yu Xiang, De-Cai Shao, Qing-Yong Zhang, Bin Liu, Shao-Na Hong, Qiong-Hua Quan, Guo-Bo Wu, Guo-Quan Sci Rep Article Mammalian oocytes represent impaired quality after undergoing a process of postovulatory aging, which can be alleviated through various effective ways such as reagent treatment. Accumulating evidences have revealed the beneficial effects of astaxanthin (Ax) as a potential antioxidant on reproductive biology. Here, porcine matured oocytes were used as a model to explore whether Ax supplement can protect against oocyte aging in vitro and the underlying mechanism, and therefore they were cultured with or without 2.5 μM Ax for an additional 24 h. Aged oocytes treated with Ax showed improved yield and quality of blastocysts as well as recovered expression of maternal genes. Importantly, oxidative stress in aged oocytes was relieved through Ax treatment, based on reduced reactive oxygen species and enhanced glutathione and antioxidant gene expression. Moreover, inhibition in apoptosis and autophagy of aged oocyte by Ax was confirmed through decreased caspase-3, cathepsin B and autophagic activities. Ax could also maintain spindle organization and actin expression, and rescue functional status of organelles including mitochondria, endoplasmic reticulum, Golgi apparatus and lysosomes according to restored fluorescence intensity. In conclusion, Ax might provide an alternative for ameliorating the oocyte quality following aging in vitro, through the mechanisms mediated by its antioxidant properties. Nature Publishing Group UK 2020-11-19 /pmc/articles/PMC7677382/ /pubmed/33214659 http://dx.doi.org/10.1038/s41598-020-77359-6 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Jia, Bao-Yu Xiang, De-Cai Shao, Qing-Yong Zhang, Bin Liu, Shao-Na Hong, Qiong-Hua Quan, Guo-Bo Wu, Guo-Quan Inhibitory effects of astaxanthin on postovulatory porcine oocyte aging in vitro |
title | Inhibitory effects of astaxanthin on postovulatory porcine oocyte aging in vitro |
title_full | Inhibitory effects of astaxanthin on postovulatory porcine oocyte aging in vitro |
title_fullStr | Inhibitory effects of astaxanthin on postovulatory porcine oocyte aging in vitro |
title_full_unstemmed | Inhibitory effects of astaxanthin on postovulatory porcine oocyte aging in vitro |
title_short | Inhibitory effects of astaxanthin on postovulatory porcine oocyte aging in vitro |
title_sort | inhibitory effects of astaxanthin on postovulatory porcine oocyte aging in vitro |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7677382/ https://www.ncbi.nlm.nih.gov/pubmed/33214659 http://dx.doi.org/10.1038/s41598-020-77359-6 |
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