Cargando…

Grape Seed Proanthocyanidin Ameliorates FB(1)-Induced Meiotic Defects in Porcine Oocytes

Fumonisin B(1) (FB(1)), as the most prevalent and toxic fumonisin, poses a health threat to humans and animals. The cytotoxicity of FB(1) is closely related to oxidative stress and apoptosis. The purpose of this study is to explore whether Grape seed proanthocyanidin (GSP), a natural antioxidant, co...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Wenhui, He, Yijing, Zhao, Hongyu, Peng, Lei, Li, Jia, Rui, Rong, Ju, Shiqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8706835/
https://www.ncbi.nlm.nih.gov/pubmed/34941679
http://dx.doi.org/10.3390/toxins13120841
_version_ 1784622288830726144
author Li, Wenhui
He, Yijing
Zhao, Hongyu
Peng, Lei
Li, Jia
Rui, Rong
Ju, Shiqiang
author_facet Li, Wenhui
He, Yijing
Zhao, Hongyu
Peng, Lei
Li, Jia
Rui, Rong
Ju, Shiqiang
author_sort Li, Wenhui
collection PubMed
description Fumonisin B(1) (FB(1)), as the most prevalent and toxic fumonisin, poses a health threat to humans and animals. The cytotoxicity of FB(1) is closely related to oxidative stress and apoptosis. The purpose of this study is to explore whether Grape seed proanthocyanidin (GSP), a natural antioxidant, could alleviate the meiotic maturation defects of oocytes caused by FB(1) exposure. Porcine cumulus oocyte complexes (COCs) were treated with 30 μM FB(1) alone or cotreated with 100, 200 and 300 μM GSP during in vitro maturation for 44 h. The results show that 200 μM GSP cotreatment observably ameliorated the toxic effects of FB(1) exposure, showing to be promoting first polar body extrusion and improving the subsequent cleavage rate and blastocyst development rate. Moreover, 200 μM GSP cotreatment restored cell cycle progression, reduced the proportion of aberrant spindles, improved actin distribution and protected mitochondrial function in FB(1)-exposed oocytes. Furthermore, reactive oxygen species (ROS) generation was significantly decreased and the mRNA levels of CAT, SOD2 and GSH-PX were obviously increased in the 200 μM GSP cotreatment group. Notably, the incidence of early apoptosis and autophagy level were also significantly decreased after GSP cotreatment and the mRNA expression levels of BAX, CASPASE3, LC3 and ATG5 were markedly decreased, whereas BCL2 and mTOR were observably increased in the oocytes after GSP cotreatment. Together, these results indicate that GSP could exert significant preventive effects on FB(1)-induced oocyte defects by ameliorating oxidative stress through repairing mitochondrial dysfunction.
format Online
Article
Text
id pubmed-8706835
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-87068352021-12-25 Grape Seed Proanthocyanidin Ameliorates FB(1)-Induced Meiotic Defects in Porcine Oocytes Li, Wenhui He, Yijing Zhao, Hongyu Peng, Lei Li, Jia Rui, Rong Ju, Shiqiang Toxins (Basel) Article Fumonisin B(1) (FB(1)), as the most prevalent and toxic fumonisin, poses a health threat to humans and animals. The cytotoxicity of FB(1) is closely related to oxidative stress and apoptosis. The purpose of this study is to explore whether Grape seed proanthocyanidin (GSP), a natural antioxidant, could alleviate the meiotic maturation defects of oocytes caused by FB(1) exposure. Porcine cumulus oocyte complexes (COCs) were treated with 30 μM FB(1) alone or cotreated with 100, 200 and 300 μM GSP during in vitro maturation for 44 h. The results show that 200 μM GSP cotreatment observably ameliorated the toxic effects of FB(1) exposure, showing to be promoting first polar body extrusion and improving the subsequent cleavage rate and blastocyst development rate. Moreover, 200 μM GSP cotreatment restored cell cycle progression, reduced the proportion of aberrant spindles, improved actin distribution and protected mitochondrial function in FB(1)-exposed oocytes. Furthermore, reactive oxygen species (ROS) generation was significantly decreased and the mRNA levels of CAT, SOD2 and GSH-PX were obviously increased in the 200 μM GSP cotreatment group. Notably, the incidence of early apoptosis and autophagy level were also significantly decreased after GSP cotreatment and the mRNA expression levels of BAX, CASPASE3, LC3 and ATG5 were markedly decreased, whereas BCL2 and mTOR were observably increased in the oocytes after GSP cotreatment. Together, these results indicate that GSP could exert significant preventive effects on FB(1)-induced oocyte defects by ameliorating oxidative stress through repairing mitochondrial dysfunction. MDPI 2021-11-25 /pmc/articles/PMC8706835/ /pubmed/34941679 http://dx.doi.org/10.3390/toxins13120841 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
Li, Wenhui
He, Yijing
Zhao, Hongyu
Peng, Lei
Li, Jia
Rui, Rong
Ju, Shiqiang
Grape Seed Proanthocyanidin Ameliorates FB(1)-Induced Meiotic Defects in Porcine Oocytes
title Grape Seed Proanthocyanidin Ameliorates FB(1)-Induced Meiotic Defects in Porcine Oocytes
title_full Grape Seed Proanthocyanidin Ameliorates FB(1)-Induced Meiotic Defects in Porcine Oocytes
title_fullStr Grape Seed Proanthocyanidin Ameliorates FB(1)-Induced Meiotic Defects in Porcine Oocytes
title_full_unstemmed Grape Seed Proanthocyanidin Ameliorates FB(1)-Induced Meiotic Defects in Porcine Oocytes
title_short Grape Seed Proanthocyanidin Ameliorates FB(1)-Induced Meiotic Defects in Porcine Oocytes
title_sort grape seed proanthocyanidin ameliorates fb(1)-induced meiotic defects in porcine oocytes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8706835/
https://www.ncbi.nlm.nih.gov/pubmed/34941679
http://dx.doi.org/10.3390/toxins13120841
work_keys_str_mv AT liwenhui grapeseedproanthocyanidinamelioratesfb1inducedmeioticdefectsinporcineoocytes
AT heyijing grapeseedproanthocyanidinamelioratesfb1inducedmeioticdefectsinporcineoocytes
AT zhaohongyu grapeseedproanthocyanidinamelioratesfb1inducedmeioticdefectsinporcineoocytes
AT penglei grapeseedproanthocyanidinamelioratesfb1inducedmeioticdefectsinporcineoocytes
AT lijia grapeseedproanthocyanidinamelioratesfb1inducedmeioticdefectsinporcineoocytes
AT ruirong grapeseedproanthocyanidinamelioratesfb1inducedmeioticdefectsinporcineoocytes
AT jushiqiang grapeseedproanthocyanidinamelioratesfb1inducedmeioticdefectsinporcineoocytes