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Carnosic acid improves porcine early embryonic development by inhibiting the accumulation of reactive oxygen species
Carnosic acid (CA), a natural catechol rosin diterpene, is used as an additive in animal feeds and human foods. However, the effects of CA on mammalian reproductive processes, especially early embryonic development, are unclear. In this study, we added CA to parthenogenetically activated porcine emb...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Society for Reproduction and Development
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7768177/ https://www.ncbi.nlm.nih.gov/pubmed/33055461 http://dx.doi.org/10.1262/jrd.2020-086 |
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author | PENG, Yan-xia CHEN, Cheng-Zhen LUO, Dan YU, Wen-jie LI, Sheng-peng XIAO, Yue YUAN, Bao LIANG, Shuang YAO, Xue-rui KIM, Nam-Hyung JIANG, Hao ZHANG, Jia-Bao |
author_facet | PENG, Yan-xia CHEN, Cheng-Zhen LUO, Dan YU, Wen-jie LI, Sheng-peng XIAO, Yue YUAN, Bao LIANG, Shuang YAO, Xue-rui KIM, Nam-Hyung JIANG, Hao ZHANG, Jia-Bao |
author_sort | PENG, Yan-xia |
collection | PubMed |
description | Carnosic acid (CA), a natural catechol rosin diterpene, is used as an additive in animal feeds and human foods. However, the effects of CA on mammalian reproductive processes, especially early embryonic development, are unclear. In this study, we added CA to parthenogenetically activated porcine embryos in an in vitro culture medium to explore the influence of CA on apoptosis, proliferation, blastocyst formation, reactive oxygen species (ROS) levels, glutathione (GSH) levels, mitochondrial membrane potential, and embryonic development-related gene expression. The results showed that supplementation with 10 μM CA during in vitro culture significantly improved the cleavage rates, blastocyst formation rates, hatching rates, and total numbers of cells of parthenogenetically activated porcine embryos compared with no supplementation. More importantly, supplementation with CA also improved GSH levels and mitochondrial membrane potential, reduced natural ROS levels in blastomeres, upregulated Nanog, Sox2, Gata4, Cox2, Itga5, and Rictor expression, and downregulated Birc5 and Caspase3 expression. These results suggest that CA can improve early porcine embryonic development by regulating oxidative stress. This study elucidates the effects of CA on early embryonic development and their potential mechanisms, and provides new applications for improving the quality of in vitro-developed embryos. |
format | Online Article Text |
id | pubmed-7768177 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Society for Reproduction and Development |
record_format | MEDLINE/PubMed |
spelling | pubmed-77681772020-12-31 Carnosic acid improves porcine early embryonic development by inhibiting the accumulation of reactive oxygen species PENG, Yan-xia CHEN, Cheng-Zhen LUO, Dan YU, Wen-jie LI, Sheng-peng XIAO, Yue YUAN, Bao LIANG, Shuang YAO, Xue-rui KIM, Nam-Hyung JIANG, Hao ZHANG, Jia-Bao J Reprod Dev Original Article Carnosic acid (CA), a natural catechol rosin diterpene, is used as an additive in animal feeds and human foods. However, the effects of CA on mammalian reproductive processes, especially early embryonic development, are unclear. In this study, we added CA to parthenogenetically activated porcine embryos in an in vitro culture medium to explore the influence of CA on apoptosis, proliferation, blastocyst formation, reactive oxygen species (ROS) levels, glutathione (GSH) levels, mitochondrial membrane potential, and embryonic development-related gene expression. The results showed that supplementation with 10 μM CA during in vitro culture significantly improved the cleavage rates, blastocyst formation rates, hatching rates, and total numbers of cells of parthenogenetically activated porcine embryos compared with no supplementation. More importantly, supplementation with CA also improved GSH levels and mitochondrial membrane potential, reduced natural ROS levels in blastomeres, upregulated Nanog, Sox2, Gata4, Cox2, Itga5, and Rictor expression, and downregulated Birc5 and Caspase3 expression. These results suggest that CA can improve early porcine embryonic development by regulating oxidative stress. This study elucidates the effects of CA on early embryonic development and their potential mechanisms, and provides new applications for improving the quality of in vitro-developed embryos. The Society for Reproduction and Development 2020-10-14 2020-12 /pmc/articles/PMC7768177/ /pubmed/33055461 http://dx.doi.org/10.1262/jrd.2020-086 Text en ©2020 Society for Reproduction and Development This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Original Article PENG, Yan-xia CHEN, Cheng-Zhen LUO, Dan YU, Wen-jie LI, Sheng-peng XIAO, Yue YUAN, Bao LIANG, Shuang YAO, Xue-rui KIM, Nam-Hyung JIANG, Hao ZHANG, Jia-Bao Carnosic acid improves porcine early embryonic development by inhibiting the accumulation of reactive oxygen species |
title | Carnosic acid improves porcine early embryonic development by inhibiting the accumulation of reactive oxygen species |
title_full | Carnosic acid improves porcine early embryonic development by inhibiting the accumulation of reactive oxygen species |
title_fullStr | Carnosic acid improves porcine early embryonic development by inhibiting the accumulation of reactive oxygen species |
title_full_unstemmed | Carnosic acid improves porcine early embryonic development by inhibiting the accumulation of reactive oxygen species |
title_short | Carnosic acid improves porcine early embryonic development by inhibiting the accumulation of reactive oxygen species |
title_sort | carnosic acid improves porcine early embryonic development by inhibiting the accumulation of reactive oxygen species |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7768177/ https://www.ncbi.nlm.nih.gov/pubmed/33055461 http://dx.doi.org/10.1262/jrd.2020-086 |
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