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Effect of Triclosan Exposure on Developmental Competence in Parthenogenetic Porcine Embryo during Preimplantation
Triclosan (TCS) is included in various healthcare products because of its antimicrobial activity; therefore, many humans are exposed to TCS daily. While detrimental effects of TCS exposure have been reported in various species and cell types, the effects of TCS exposure on early embryonic developmen...
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/PMC7461051/ https://www.ncbi.nlm.nih.gov/pubmed/32806749 http://dx.doi.org/10.3390/ijms21165790 |
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author | Kim, Min Ju Park, Hyo-Jin Lee, Sanghoon Kang, Hyo-Gu Jeong, Pil-Soo Park, Soo Hyun Park, Young-Ho Lee, Jong-Hee Lim, Kyung Seob Lee, Seung Hwan Sim, Bo-Woong Kim, Sun-Uk Cho, Seong-Keun Koo, Deog-Bon Song, Bong-Seok |
author_facet | Kim, Min Ju Park, Hyo-Jin Lee, Sanghoon Kang, Hyo-Gu Jeong, Pil-Soo Park, Soo Hyun Park, Young-Ho Lee, Jong-Hee Lim, Kyung Seob Lee, Seung Hwan Sim, Bo-Woong Kim, Sun-Uk Cho, Seong-Keun Koo, Deog-Bon Song, Bong-Seok |
author_sort | Kim, Min Ju |
collection | PubMed |
description | Triclosan (TCS) is included in various healthcare products because of its antimicrobial activity; therefore, many humans are exposed to TCS daily. While detrimental effects of TCS exposure have been reported in various species and cell types, the effects of TCS exposure on early embryonic development are largely unknown. The aim of this study was to determine if TCS exerts toxic effects during early embryonic development using porcine parthenogenetic embryos in vitro. Porcine parthenogenetic embryos were cultured in in vitro culture medium with 50 or 100 µM TCS for 6 days. Developmental parameters including cleavage and blastocyst formation rates, developmental kinetics, and the number of blastomeres were assessed. To determine the toxic effects of TCS, apoptosis, oxidative stress, and mitochondrial dysfunction were assessed. TCS exposure resulted in a significant decrease in 2-cell rate and blastocyst formation rate, as well as number of blastomeres, but not in the cleavage rate. TCS also increased the number of apoptotic blastomeres and the production of reactive oxygen species. Finally, TCS treatment resulted in a diffuse distribution of mitochondria and decreased the mitochondrial membrane potential. Our results showed that TCS exposure impaired porcine early embryonic development by inducing DNA damage, oxidative stress, and mitochondrial dysfunction. |
format | Online Article Text |
id | pubmed-7461051 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-74610512020-09-14 Effect of Triclosan Exposure on Developmental Competence in Parthenogenetic Porcine Embryo during Preimplantation Kim, Min Ju Park, Hyo-Jin Lee, Sanghoon Kang, Hyo-Gu Jeong, Pil-Soo Park, Soo Hyun Park, Young-Ho Lee, Jong-Hee Lim, Kyung Seob Lee, Seung Hwan Sim, Bo-Woong Kim, Sun-Uk Cho, Seong-Keun Koo, Deog-Bon Song, Bong-Seok Int J Mol Sci Article Triclosan (TCS) is included in various healthcare products because of its antimicrobial activity; therefore, many humans are exposed to TCS daily. While detrimental effects of TCS exposure have been reported in various species and cell types, the effects of TCS exposure on early embryonic development are largely unknown. The aim of this study was to determine if TCS exerts toxic effects during early embryonic development using porcine parthenogenetic embryos in vitro. Porcine parthenogenetic embryos were cultured in in vitro culture medium with 50 or 100 µM TCS for 6 days. Developmental parameters including cleavage and blastocyst formation rates, developmental kinetics, and the number of blastomeres were assessed. To determine the toxic effects of TCS, apoptosis, oxidative stress, and mitochondrial dysfunction were assessed. TCS exposure resulted in a significant decrease in 2-cell rate and blastocyst formation rate, as well as number of blastomeres, but not in the cleavage rate. TCS also increased the number of apoptotic blastomeres and the production of reactive oxygen species. Finally, TCS treatment resulted in a diffuse distribution of mitochondria and decreased the mitochondrial membrane potential. Our results showed that TCS exposure impaired porcine early embryonic development by inducing DNA damage, oxidative stress, and mitochondrial dysfunction. MDPI 2020-08-12 /pmc/articles/PMC7461051/ /pubmed/32806749 http://dx.doi.org/10.3390/ijms21165790 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 Kim, Min Ju Park, Hyo-Jin Lee, Sanghoon Kang, Hyo-Gu Jeong, Pil-Soo Park, Soo Hyun Park, Young-Ho Lee, Jong-Hee Lim, Kyung Seob Lee, Seung Hwan Sim, Bo-Woong Kim, Sun-Uk Cho, Seong-Keun Koo, Deog-Bon Song, Bong-Seok Effect of Triclosan Exposure on Developmental Competence in Parthenogenetic Porcine Embryo during Preimplantation |
title | Effect of Triclosan Exposure on Developmental Competence in Parthenogenetic Porcine Embryo during Preimplantation |
title_full | Effect of Triclosan Exposure on Developmental Competence in Parthenogenetic Porcine Embryo during Preimplantation |
title_fullStr | Effect of Triclosan Exposure on Developmental Competence in Parthenogenetic Porcine Embryo during Preimplantation |
title_full_unstemmed | Effect of Triclosan Exposure on Developmental Competence in Parthenogenetic Porcine Embryo during Preimplantation |
title_short | Effect of Triclosan Exposure on Developmental Competence in Parthenogenetic Porcine Embryo during Preimplantation |
title_sort | effect of triclosan exposure on developmental competence in parthenogenetic porcine embryo during preimplantation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7461051/ https://www.ncbi.nlm.nih.gov/pubmed/32806749 http://dx.doi.org/10.3390/ijms21165790 |
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