author_facet Yang, Bei
Wang, Xinlu
Ma, Yilin
Yan, Lei
Ren, Yuan
Yu, Dainan
Qiao, Bo
Shen, Xin
Liu, Hui
Zhang, Dalei
Kuang, Haibin
Yang, Bei
Wang, Xinlu
Ma, Yilin
Yan, Lei
Ren, Yuan
Yu, Dainan
Qiao, Bo
Shen, Xin
Liu, Hui
Zhang, Dalei
Kuang, Haibin
author Yang, Bei
Wang, Xinlu
Ma, Yilin
Yan, Lei
Ren, Yuan
Yu, Dainan
Qiao, Bo
Shen, Xin
Liu, Hui
Zhang, Dalei
Kuang, Haibin
spellingShingle Yang, Bei
Wang, Xinlu
Ma, Yilin
Yan, Lei
Ren, Yuan
Yu, Dainan
Qiao, Bo
Shen, Xin
Liu, Hui
Zhang, Dalei
Kuang, Haibin
Environmental Toxicology
Tri‐ortho‐cresyl phosphate (TOCP)‐induced reproductive toxicity involved in placental apoptosis, autophagy and oxidative stress in pregnant mice
Health, Toxicology and Mutagenesis
Management, Monitoring, Policy and Law
Toxicology
General Medicine
author_sort yang, bei
spelling Yang, Bei Wang, Xinlu Ma, Yilin Yan, Lei Ren, Yuan Yu, Dainan Qiao, Bo Shen, Xin Liu, Hui Zhang, Dalei Kuang, Haibin 1520-4081 1522-7278 Wiley Health, Toxicology and Mutagenesis Management, Monitoring, Policy and Law Toxicology General Medicine http://dx.doi.org/10.1002/tox.22846 <jats:title>Abstract</jats:title><jats:p>Tri‐ortho‐cresyl phosphate (TOCP) has been widely used as plasticizers, and reported causing reproductive toxicity in mammals. However, little is known about the toxic effect on the placenta. In this study, dams were orally administered different doses of TOCP to explore the effect of TOCP on placental development. Results showed that TOCP exposure significantly reduced numbers of implanted embryo, caused atrophy and collapse of ectoplacental cone, and decreased total areas of placenta and numbers of PCNA‐positive cells. Expression levels of placental development genes were prominently downregulated in the TOCP‐treated groups. Moreover, TOCP administration induced placental apoptosis and autophagy by upregulating P53, Bax, Beclin‐1, ratio of LC3 II/LC3 I and Atg5 and downregulating Bcl‐2 protein. In addition, TOCP exposure markedly inhibited activities of catalase and superoxide dismutase and increased the production of H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> and malondialdehyde. Collectively, these findings suggest that apoptosis, autophagy and oxidative stress may be involved in the TOCP‐induced reproductive toxicity.</jats:p> Tri‐ortho‐cresyl phosphate (TOCP)‐induced reproductive toxicity involved in placental apoptosis, autophagy and oxidative stress in pregnant mice Environmental Toxicology
doi_str_mv 10.1002/tox.22846
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series Environmental Toxicology
source_id 49
title Tri‐ortho‐cresyl phosphate (TOCP)‐induced reproductive toxicity involved in placental apoptosis, autophagy and oxidative stress in pregnant mice
title_unstemmed Tri‐ortho‐cresyl phosphate (TOCP)‐induced reproductive toxicity involved in placental apoptosis, autophagy and oxidative stress in pregnant mice
title_full Tri‐ortho‐cresyl phosphate (TOCP)‐induced reproductive toxicity involved in placental apoptosis, autophagy and oxidative stress in pregnant mice
title_fullStr Tri‐ortho‐cresyl phosphate (TOCP)‐induced reproductive toxicity involved in placental apoptosis, autophagy and oxidative stress in pregnant mice
title_full_unstemmed Tri‐ortho‐cresyl phosphate (TOCP)‐induced reproductive toxicity involved in placental apoptosis, autophagy and oxidative stress in pregnant mice
title_short Tri‐ortho‐cresyl phosphate (TOCP)‐induced reproductive toxicity involved in placental apoptosis, autophagy and oxidative stress in pregnant mice
title_sort tri‐ortho‐cresyl phosphate (tocp)‐induced reproductive toxicity involved in placental apoptosis, autophagy and oxidative stress in pregnant mice
topic Health, Toxicology and Mutagenesis
Management, Monitoring, Policy and Law
Toxicology
General Medicine
url http://dx.doi.org/10.1002/tox.22846
publishDate 2020
physical 97-107
description <jats:title>Abstract</jats:title><jats:p>Tri‐ortho‐cresyl phosphate (TOCP) has been widely used as plasticizers, and reported causing reproductive toxicity in mammals. However, little is known about the toxic effect on the placenta. In this study, dams were orally administered different doses of TOCP to explore the effect of TOCP on placental development. Results showed that TOCP exposure significantly reduced numbers of implanted embryo, caused atrophy and collapse of ectoplacental cone, and decreased total areas of placenta and numbers of PCNA‐positive cells. Expression levels of placental development genes were prominently downregulated in the TOCP‐treated groups. Moreover, TOCP administration induced placental apoptosis and autophagy by upregulating P53, Bax, Beclin‐1, ratio of LC3 II/LC3 I and Atg5 and downregulating Bcl‐2 protein. In addition, TOCP exposure markedly inhibited activities of catalase and superoxide dismutase and increased the production of H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> and malondialdehyde. Collectively, these findings suggest that apoptosis, autophagy and oxidative stress may be involved in the TOCP‐induced reproductive toxicity.</jats:p>
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author Yang, Bei, Wang, Xinlu, Ma, Yilin, Yan, Lei, Ren, Yuan, Yu, Dainan, Qiao, Bo, Shen, Xin, Liu, Hui, Zhang, Dalei, Kuang, Haibin
author_facet Yang, Bei, Wang, Xinlu, Ma, Yilin, Yan, Lei, Ren, Yuan, Yu, Dainan, Qiao, Bo, Shen, Xin, Liu, Hui, Zhang, Dalei, Kuang, Haibin, Yang, Bei, Wang, Xinlu, Ma, Yilin, Yan, Lei, Ren, Yuan, Yu, Dainan, Qiao, Bo, Shen, Xin, Liu, Hui, Zhang, Dalei, Kuang, Haibin
author_sort yang, bei
container_issue 1
container_start_page 97
container_title Environmental Toxicology
container_volume 35
description <jats:title>Abstract</jats:title><jats:p>Tri‐ortho‐cresyl phosphate (TOCP) has been widely used as plasticizers, and reported causing reproductive toxicity in mammals. However, little is known about the toxic effect on the placenta. In this study, dams were orally administered different doses of TOCP to explore the effect of TOCP on placental development. Results showed that TOCP exposure significantly reduced numbers of implanted embryo, caused atrophy and collapse of ectoplacental cone, and decreased total areas of placenta and numbers of PCNA‐positive cells. Expression levels of placental development genes were prominently downregulated in the TOCP‐treated groups. Moreover, TOCP administration induced placental apoptosis and autophagy by upregulating P53, Bax, Beclin‐1, ratio of LC3 II/LC3 I and Atg5 and downregulating Bcl‐2 protein. In addition, TOCP exposure markedly inhibited activities of catalase and superoxide dismutase and increased the production of H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> and malondialdehyde. Collectively, these findings suggest that apoptosis, autophagy and oxidative stress may be involved in the TOCP‐induced reproductive toxicity.</jats:p>
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spelling Yang, Bei Wang, Xinlu Ma, Yilin Yan, Lei Ren, Yuan Yu, Dainan Qiao, Bo Shen, Xin Liu, Hui Zhang, Dalei Kuang, Haibin 1520-4081 1522-7278 Wiley Health, Toxicology and Mutagenesis Management, Monitoring, Policy and Law Toxicology General Medicine http://dx.doi.org/10.1002/tox.22846 <jats:title>Abstract</jats:title><jats:p>Tri‐ortho‐cresyl phosphate (TOCP) has been widely used as plasticizers, and reported causing reproductive toxicity in mammals. However, little is known about the toxic effect on the placenta. In this study, dams were orally administered different doses of TOCP to explore the effect of TOCP on placental development. Results showed that TOCP exposure significantly reduced numbers of implanted embryo, caused atrophy and collapse of ectoplacental cone, and decreased total areas of placenta and numbers of PCNA‐positive cells. Expression levels of placental development genes were prominently downregulated in the TOCP‐treated groups. Moreover, TOCP administration induced placental apoptosis and autophagy by upregulating P53, Bax, Beclin‐1, ratio of LC3 II/LC3 I and Atg5 and downregulating Bcl‐2 protein. In addition, TOCP exposure markedly inhibited activities of catalase and superoxide dismutase and increased the production of H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub> and malondialdehyde. Collectively, these findings suggest that apoptosis, autophagy and oxidative stress may be involved in the TOCP‐induced reproductive toxicity.</jats:p> Tri‐ortho‐cresyl phosphate (TOCP)‐induced reproductive toxicity involved in placental apoptosis, autophagy and oxidative stress in pregnant mice Environmental Toxicology
spellingShingle Yang, Bei, Wang, Xinlu, Ma, Yilin, Yan, Lei, Ren, Yuan, Yu, Dainan, Qiao, Bo, Shen, Xin, Liu, Hui, Zhang, Dalei, Kuang, Haibin, Environmental Toxicology, Tri‐ortho‐cresyl phosphate (TOCP)‐induced reproductive toxicity involved in placental apoptosis, autophagy and oxidative stress in pregnant mice, Health, Toxicology and Mutagenesis, Management, Monitoring, Policy and Law, Toxicology, General Medicine
title Tri‐ortho‐cresyl phosphate (TOCP)‐induced reproductive toxicity involved in placental apoptosis, autophagy and oxidative stress in pregnant mice
title_full Tri‐ortho‐cresyl phosphate (TOCP)‐induced reproductive toxicity involved in placental apoptosis, autophagy and oxidative stress in pregnant mice
title_fullStr Tri‐ortho‐cresyl phosphate (TOCP)‐induced reproductive toxicity involved in placental apoptosis, autophagy and oxidative stress in pregnant mice
title_full_unstemmed Tri‐ortho‐cresyl phosphate (TOCP)‐induced reproductive toxicity involved in placental apoptosis, autophagy and oxidative stress in pregnant mice
title_short Tri‐ortho‐cresyl phosphate (TOCP)‐induced reproductive toxicity involved in placental apoptosis, autophagy and oxidative stress in pregnant mice
title_sort tri‐ortho‐cresyl phosphate (tocp)‐induced reproductive toxicity involved in placental apoptosis, autophagy and oxidative stress in pregnant mice
title_unstemmed Tri‐ortho‐cresyl phosphate (TOCP)‐induced reproductive toxicity involved in placental apoptosis, autophagy and oxidative stress in pregnant mice
topic Health, Toxicology and Mutagenesis, Management, Monitoring, Policy and Law, Toxicology, General Medicine
url http://dx.doi.org/10.1002/tox.22846