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Resveratrol Improves the Mitochondrial Function and Fertilization Outcome of Bovine Oocytes

The aim of the present study was to address the effect of resveratrol-mediated upregulation of sirtuin 1 (SIRT1) during oocyte maturation on mitochondrial function, the developmental ability of oocytes and on mechanisms responsible for blockage of polyspermic fertilization. Oocytes collected from sl...

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Autores principales: TAKEO, Shun, SATO, Daichi, KIMURA, Koji, MONJI, Yasunori, KUWAYAMA, Takehito, KAWAHARA-MIKI, Ryoka, IWATA, Hisataka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Society for Reproduction and Development 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3999399/
https://www.ncbi.nlm.nih.gov/pubmed/24390595
http://dx.doi.org/10.1262/jrd.2013-102
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author TAKEO, Shun
SATO, Daichi
KIMURA, Koji
MONJI, Yasunori
KUWAYAMA, Takehito
KAWAHARA-MIKI, Ryoka
IWATA, Hisataka
author_facet TAKEO, Shun
SATO, Daichi
KIMURA, Koji
MONJI, Yasunori
KUWAYAMA, Takehito
KAWAHARA-MIKI, Ryoka
IWATA, Hisataka
author_sort TAKEO, Shun
collection PubMed
description The aim of the present study was to address the effect of resveratrol-mediated upregulation of sirtuin 1 (SIRT1) during oocyte maturation on mitochondrial function, the developmental ability of oocytes and on mechanisms responsible for blockage of polyspermic fertilization. Oocytes collected from slaughterhouse-derived ovaries were cultured in TCM-199 medium supplemented with 10% FCS and 0 or 20 µM resveratrol (Res). We examined the effect of Res on SIRT1 expression in in vitro-matured oocytes (Exp 1); fertilization and developmental ability (Exp 2); mitochondrial DNA copy number (Mt number), ATP content and mitochondrial membrane potential in matured oocytes (Exp 3); and the time required for proteinase to dissolve the zona pellucida following in vitro fertilization (as a marker of zona pellucida hardening), as well as on the distribution of cortical granules before and after fertilization (Exp 4). In Exp 1, the 20 µM Res treatment upregulated protein expression of SIRT1 in oocytes. In Exp 2, Res treatment improved the ratio of normal fertilization and the total cell number of blastocysts. In Exp 3, Res treatment significantly increased the ATP content in matured oocytes. Additionally, Res increased the overall Mt number and mitochondrial membrane potential, but the effect was donor-dependent. In Exp 4, Res-induced zona hardening improved the distribution and exocytosis of cortical granules after in vitro fertilization. In conclusion, Res improved the quality of oocytes by improving mitochondrial quantity and quality. In addition, Res added to the maturation medium enhanced SIRT1 protein expression in oocytes and improved fertilization via reinforcement of the mechanisms responsible for blockage of polyspermic fertilization.
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spelling pubmed-39993992014-04-25 Resveratrol Improves the Mitochondrial Function and Fertilization Outcome of Bovine Oocytes TAKEO, Shun SATO, Daichi KIMURA, Koji MONJI, Yasunori KUWAYAMA, Takehito KAWAHARA-MIKI, Ryoka IWATA, Hisataka J Reprod Dev Original Article The aim of the present study was to address the effect of resveratrol-mediated upregulation of sirtuin 1 (SIRT1) during oocyte maturation on mitochondrial function, the developmental ability of oocytes and on mechanisms responsible for blockage of polyspermic fertilization. Oocytes collected from slaughterhouse-derived ovaries were cultured in TCM-199 medium supplemented with 10% FCS and 0 or 20 µM resveratrol (Res). We examined the effect of Res on SIRT1 expression in in vitro-matured oocytes (Exp 1); fertilization and developmental ability (Exp 2); mitochondrial DNA copy number (Mt number), ATP content and mitochondrial membrane potential in matured oocytes (Exp 3); and the time required for proteinase to dissolve the zona pellucida following in vitro fertilization (as a marker of zona pellucida hardening), as well as on the distribution of cortical granules before and after fertilization (Exp 4). In Exp 1, the 20 µM Res treatment upregulated protein expression of SIRT1 in oocytes. In Exp 2, Res treatment improved the ratio of normal fertilization and the total cell number of blastocysts. In Exp 3, Res treatment significantly increased the ATP content in matured oocytes. Additionally, Res increased the overall Mt number and mitochondrial membrane potential, but the effect was donor-dependent. In Exp 4, Res-induced zona hardening improved the distribution and exocytosis of cortical granules after in vitro fertilization. In conclusion, Res improved the quality of oocytes by improving mitochondrial quantity and quality. In addition, Res added to the maturation medium enhanced SIRT1 protein expression in oocytes and improved fertilization via reinforcement of the mechanisms responsible for blockage of polyspermic fertilization. The Society for Reproduction and Development 2013-12-27 2014-04 /pmc/articles/PMC3999399/ /pubmed/24390595 http://dx.doi.org/10.1262/jrd.2013-102 Text en ©2014 Society for Reproduction and Development http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License.
spellingShingle Original Article
TAKEO, Shun
SATO, Daichi
KIMURA, Koji
MONJI, Yasunori
KUWAYAMA, Takehito
KAWAHARA-MIKI, Ryoka
IWATA, Hisataka
Resveratrol Improves the Mitochondrial Function and Fertilization Outcome of Bovine Oocytes
title Resveratrol Improves the Mitochondrial Function and Fertilization Outcome of Bovine Oocytes
title_full Resveratrol Improves the Mitochondrial Function and Fertilization Outcome of Bovine Oocytes
title_fullStr Resveratrol Improves the Mitochondrial Function and Fertilization Outcome of Bovine Oocytes
title_full_unstemmed Resveratrol Improves the Mitochondrial Function and Fertilization Outcome of Bovine Oocytes
title_short Resveratrol Improves the Mitochondrial Function and Fertilization Outcome of Bovine Oocytes
title_sort resveratrol improves the mitochondrial function and fertilization outcome of bovine oocytes
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3999399/
https://www.ncbi.nlm.nih.gov/pubmed/24390595
http://dx.doi.org/10.1262/jrd.2013-102
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