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Butylparaben Is Toxic to Porcine Oocyte Maturation and Subsequent Embryonic Development Following In Vitro Fertilization
Parabens are widely used in personal care products due to their antimicrobial effects. Although the toxicity of parabens has been reported, little information is available on the toxicity of butylparaben (BP) on oocyte maturation. Therefore, we investigated the effects of various concentrations of B...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7279239/ https://www.ncbi.nlm.nih.gov/pubmed/32456265 http://dx.doi.org/10.3390/ijms21103692 |
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author | Jeong, Pil-Soo Lee, Sanghoon Park, Soo-Hyun Kim, Min Ju Kang, Hyo-Gu Nanjidsuren, Tsevelmaa Son, Hee-Chang Song, Bong-Seok Koo, Deog-Bon Sim, Bo-Woong Kim, Sun-Uk |
author_facet | Jeong, Pil-Soo Lee, Sanghoon Park, Soo-Hyun Kim, Min Ju Kang, Hyo-Gu Nanjidsuren, Tsevelmaa Son, Hee-Chang Song, Bong-Seok Koo, Deog-Bon Sim, Bo-Woong Kim, Sun-Uk |
author_sort | Jeong, Pil-Soo |
collection | PubMed |
description | Parabens are widely used in personal care products due to their antimicrobial effects. Although the toxicity of parabens has been reported, little information is available on the toxicity of butylparaben (BP) on oocyte maturation. Therefore, we investigated the effects of various concentrations of BP (0 μM, 100 μM, 200 μM, 300 μM, 400 μM, and 500 μM) on the in vitro maturation of porcine oocytes. BP supplementation at a concentration greater than 300 μM significantly reduced the proportion of complete cumulus cell expansion and metaphase II oocytes compared to the control. The 300 μM BP significantly decreased fertilization, cleavage, and blastocyst formation rates with lower total cell numbers and a higher rate of apoptosis in blastocysts compared to the control. The BP-treated oocytes showed significantly higher reactive oxygen species (ROS) levels, and lower glutathione (GSH) levels than the control. BP significantly increased the aberrant mitochondrial distribution and decreased mitochondrial function compared to the control. BP-treated oocytes exhibited significantly higher percentage of γ-H2AX, annexin V-positive oocytes and expression of LC3 than the control. In conclusion, we demonstrated that BP impaired oocyte maturation and subsequent embryonic development, by inducing ROS generation and reducing GSH levels. Furthermore, BP disrupted mitochondrial function and triggered DNA damage, early apoptosis, and autophagy in oocytes. |
format | Online Article Text |
id | pubmed-7279239 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72792392020-06-15 Butylparaben Is Toxic to Porcine Oocyte Maturation and Subsequent Embryonic Development Following In Vitro Fertilization Jeong, Pil-Soo Lee, Sanghoon Park, Soo-Hyun Kim, Min Ju Kang, Hyo-Gu Nanjidsuren, Tsevelmaa Son, Hee-Chang Song, Bong-Seok Koo, Deog-Bon Sim, Bo-Woong Kim, Sun-Uk Int J Mol Sci Article Parabens are widely used in personal care products due to their antimicrobial effects. Although the toxicity of parabens has been reported, little information is available on the toxicity of butylparaben (BP) on oocyte maturation. Therefore, we investigated the effects of various concentrations of BP (0 μM, 100 μM, 200 μM, 300 μM, 400 μM, and 500 μM) on the in vitro maturation of porcine oocytes. BP supplementation at a concentration greater than 300 μM significantly reduced the proportion of complete cumulus cell expansion and metaphase II oocytes compared to the control. The 300 μM BP significantly decreased fertilization, cleavage, and blastocyst formation rates with lower total cell numbers and a higher rate of apoptosis in blastocysts compared to the control. The BP-treated oocytes showed significantly higher reactive oxygen species (ROS) levels, and lower glutathione (GSH) levels than the control. BP significantly increased the aberrant mitochondrial distribution and decreased mitochondrial function compared to the control. BP-treated oocytes exhibited significantly higher percentage of γ-H2AX, annexin V-positive oocytes and expression of LC3 than the control. In conclusion, we demonstrated that BP impaired oocyte maturation and subsequent embryonic development, by inducing ROS generation and reducing GSH levels. Furthermore, BP disrupted mitochondrial function and triggered DNA damage, early apoptosis, and autophagy in oocytes. MDPI 2020-05-24 /pmc/articles/PMC7279239/ /pubmed/32456265 http://dx.doi.org/10.3390/ijms21103692 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Jeong, Pil-Soo Lee, Sanghoon Park, Soo-Hyun Kim, Min Ju Kang, Hyo-Gu Nanjidsuren, Tsevelmaa Son, Hee-Chang Song, Bong-Seok Koo, Deog-Bon Sim, Bo-Woong Kim, Sun-Uk Butylparaben Is Toxic to Porcine Oocyte Maturation and Subsequent Embryonic Development Following In Vitro Fertilization |
title | Butylparaben Is Toxic to Porcine Oocyte Maturation and Subsequent Embryonic Development Following In Vitro Fertilization |
title_full | Butylparaben Is Toxic to Porcine Oocyte Maturation and Subsequent Embryonic Development Following In Vitro Fertilization |
title_fullStr | Butylparaben Is Toxic to Porcine Oocyte Maturation and Subsequent Embryonic Development Following In Vitro Fertilization |
title_full_unstemmed | Butylparaben Is Toxic to Porcine Oocyte Maturation and Subsequent Embryonic Development Following In Vitro Fertilization |
title_short | Butylparaben Is Toxic to Porcine Oocyte Maturation and Subsequent Embryonic Development Following In Vitro Fertilization |
title_sort | butylparaben is toxic to porcine oocyte maturation and subsequent embryonic development following in vitro fertilization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7279239/ https://www.ncbi.nlm.nih.gov/pubmed/32456265 http://dx.doi.org/10.3390/ijms21103692 |
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