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Dihydrolipoic Acid Induces Cytotoxicity in Mouse Blastocysts through Apoptosis Processes
α-Lipoic acid (LA) is a thiol with antioxidant properties that protects against oxidative stress-induced apoptosis. LA is absorbed from the diet, taken up by cells and tissues, and subsequently reduced to dihydrolipoic acid (DHLA). In view of the recent application of DHLA as a hydrophilic nanomater...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3317754/ https://www.ncbi.nlm.nih.gov/pubmed/22489194 http://dx.doi.org/10.3390/ijms13033988 |
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author | Houng, Wei-Li Lin, Cheng-An J. Shen, Ji-Lin Yeh, Hung-I Wang, Hsueh-Hsiao Chang, Walter H. Chan, Wen-Hsiung |
author_facet | Houng, Wei-Li Lin, Cheng-An J. Shen, Ji-Lin Yeh, Hung-I Wang, Hsueh-Hsiao Chang, Walter H. Chan, Wen-Hsiung |
author_sort | Houng, Wei-Li |
collection | PubMed |
description | α-Lipoic acid (LA) is a thiol with antioxidant properties that protects against oxidative stress-induced apoptosis. LA is absorbed from the diet, taken up by cells and tissues, and subsequently reduced to dihydrolipoic acid (DHLA). In view of the recent application of DHLA as a hydrophilic nanomaterial preparation, determination of its biosafety profile is essential. In the current study, we examined the cytotoxic effects of DHLA on mouse embryos at the blastocyst stage, subsequent embryonic attachment and outgrowth in vitro, in vivo implantation by embryo transfer, and early embryonic development in an animal model. Blastocysts treated with 50 μM DHLA exhibited significantly increased apoptosis and a corresponding decrease in total cell number. Notably, the implantation success rates of blastocysts pretreated with DHLA were lower than that of their control counterparts. Moreover, in vitro treatment with 50 μM DHLA was associated with increased resorption of post-implantation embryos and decreased fetal weight. Data obtained using an in vivo mouse model further disclosed that consumption of drinking water containing 100 μM DHLA led to decreased early embryo development, specifically, inhibition of development to the blastocyst stage. However, it appears that concentrations of DHLA lower than 50 μM do not exert a hazardous effect on embryonic development. Our results collectively indicate that in vitro and in vivo exposure to concentrations of DHLA higher than 50 μM DHLA induces apoptosis and retards early pre- and post-implantation development, and support the potential of DHLA to induce embryonic cytotoxicity. |
format | Online Article Text |
id | pubmed-3317754 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-33177542012-04-09 Dihydrolipoic Acid Induces Cytotoxicity in Mouse Blastocysts through Apoptosis Processes Houng, Wei-Li Lin, Cheng-An J. Shen, Ji-Lin Yeh, Hung-I Wang, Hsueh-Hsiao Chang, Walter H. Chan, Wen-Hsiung Int J Mol Sci Article α-Lipoic acid (LA) is a thiol with antioxidant properties that protects against oxidative stress-induced apoptosis. LA is absorbed from the diet, taken up by cells and tissues, and subsequently reduced to dihydrolipoic acid (DHLA). In view of the recent application of DHLA as a hydrophilic nanomaterial preparation, determination of its biosafety profile is essential. In the current study, we examined the cytotoxic effects of DHLA on mouse embryos at the blastocyst stage, subsequent embryonic attachment and outgrowth in vitro, in vivo implantation by embryo transfer, and early embryonic development in an animal model. Blastocysts treated with 50 μM DHLA exhibited significantly increased apoptosis and a corresponding decrease in total cell number. Notably, the implantation success rates of blastocysts pretreated with DHLA were lower than that of their control counterparts. Moreover, in vitro treatment with 50 μM DHLA was associated with increased resorption of post-implantation embryos and decreased fetal weight. Data obtained using an in vivo mouse model further disclosed that consumption of drinking water containing 100 μM DHLA led to decreased early embryo development, specifically, inhibition of development to the blastocyst stage. However, it appears that concentrations of DHLA lower than 50 μM do not exert a hazardous effect on embryonic development. Our results collectively indicate that in vitro and in vivo exposure to concentrations of DHLA higher than 50 μM DHLA induces apoptosis and retards early pre- and post-implantation development, and support the potential of DHLA to induce embryonic cytotoxicity. Molecular Diversity Preservation International (MDPI) 2012-03-22 /pmc/articles/PMC3317754/ /pubmed/22489194 http://dx.doi.org/10.3390/ijms13033988 Text en © 2012 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Houng, Wei-Li Lin, Cheng-An J. Shen, Ji-Lin Yeh, Hung-I Wang, Hsueh-Hsiao Chang, Walter H. Chan, Wen-Hsiung Dihydrolipoic Acid Induces Cytotoxicity in Mouse Blastocysts through Apoptosis Processes |
title | Dihydrolipoic Acid Induces Cytotoxicity in Mouse Blastocysts through Apoptosis Processes |
title_full | Dihydrolipoic Acid Induces Cytotoxicity in Mouse Blastocysts through Apoptosis Processes |
title_fullStr | Dihydrolipoic Acid Induces Cytotoxicity in Mouse Blastocysts through Apoptosis Processes |
title_full_unstemmed | Dihydrolipoic Acid Induces Cytotoxicity in Mouse Blastocysts through Apoptosis Processes |
title_short | Dihydrolipoic Acid Induces Cytotoxicity in Mouse Blastocysts through Apoptosis Processes |
title_sort | dihydrolipoic acid induces cytotoxicity in mouse blastocysts through apoptosis processes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3317754/ https://www.ncbi.nlm.nih.gov/pubmed/22489194 http://dx.doi.org/10.3390/ijms13033988 |
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