Cargando…
Induction Effect of Bisphenol A on Gene Expression Involving Hepatic Oxidative Stress in Rat
Background and Objective. Bisphenol A (BPA) is an abundantly used xenoestrogenic chemical which may cause various disorders in body. In the present study, we sought to investigate the effects of various doses of BPA on hepatic oxidative stress-related gene expression in rats. Methods. Male Wistar ra...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4842055/ https://www.ncbi.nlm.nih.gov/pubmed/27143994 http://dx.doi.org/10.1155/2016/6298515 |
_version_ | 1782428469081145344 |
---|---|
author | Kazemi, Sohrab Mousavi, Seydeh Narges Aghapour, Fahimeh Rezaee, Boshra Sadeghi, Farzin Moghadamnia, Ali Akbar |
author_facet | Kazemi, Sohrab Mousavi, Seydeh Narges Aghapour, Fahimeh Rezaee, Boshra Sadeghi, Farzin Moghadamnia, Ali Akbar |
author_sort | Kazemi, Sohrab |
collection | PubMed |
description | Background and Objective. Bisphenol A (BPA) is an abundantly used xenoestrogenic chemical which may cause various disorders in body. In the present study, we sought to investigate the effects of various doses of BPA on hepatic oxidative stress-related gene expression in rats. Methods. Male Wistar rats weighing 150–200 g were used in this study. Three doses of the BPA (5, 25, and 125 μg/kg) in corn oil were administered as gavage during 35 consecutive days. After the experiment, the rats were expired and the livers were removed and stored at −80°C freezer for RNA extraction. Findings. The Real Time PCR showed increased expression of HO-1 in the rats receiving BPA doses compared to the control group. This effect was dose-dependent and higher at doses of 25 and 125 μg/kg than 5 μg/kg of body weight (p < 0.05). It was also demonstrated that various doses BPA can increase GADD45B gene expression compared to control group. That expression was significantly dominant in the lowest dose (5 μg/kg) of the BPA (p < 0.05). The final body weights (168.0 ± 10.0 gr) in the treatment group [BPA (125 μg/kg)] showed a significant decrease compared to control group (191.60 ± 6.50 gr). Conclusion. These findings demonstrate that BPA generated ROS and increased the antioxidant gene expression that causes hepatotoxicity. |
format | Online Article Text |
id | pubmed-4842055 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-48420552016-05-03 Induction Effect of Bisphenol A on Gene Expression Involving Hepatic Oxidative Stress in Rat Kazemi, Sohrab Mousavi, Seydeh Narges Aghapour, Fahimeh Rezaee, Boshra Sadeghi, Farzin Moghadamnia, Ali Akbar Oxid Med Cell Longev Research Article Background and Objective. Bisphenol A (BPA) is an abundantly used xenoestrogenic chemical which may cause various disorders in body. In the present study, we sought to investigate the effects of various doses of BPA on hepatic oxidative stress-related gene expression in rats. Methods. Male Wistar rats weighing 150–200 g were used in this study. Three doses of the BPA (5, 25, and 125 μg/kg) in corn oil were administered as gavage during 35 consecutive days. After the experiment, the rats were expired and the livers were removed and stored at −80°C freezer for RNA extraction. Findings. The Real Time PCR showed increased expression of HO-1 in the rats receiving BPA doses compared to the control group. This effect was dose-dependent and higher at doses of 25 and 125 μg/kg than 5 μg/kg of body weight (p < 0.05). It was also demonstrated that various doses BPA can increase GADD45B gene expression compared to control group. That expression was significantly dominant in the lowest dose (5 μg/kg) of the BPA (p < 0.05). The final body weights (168.0 ± 10.0 gr) in the treatment group [BPA (125 μg/kg)] showed a significant decrease compared to control group (191.60 ± 6.50 gr). Conclusion. These findings demonstrate that BPA generated ROS and increased the antioxidant gene expression that causes hepatotoxicity. Hindawi Publishing Corporation 2016 2016-04-10 /pmc/articles/PMC4842055/ /pubmed/27143994 http://dx.doi.org/10.1155/2016/6298515 Text en Copyright © 2016 Sohrab Kazemi et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Kazemi, Sohrab Mousavi, Seydeh Narges Aghapour, Fahimeh Rezaee, Boshra Sadeghi, Farzin Moghadamnia, Ali Akbar Induction Effect of Bisphenol A on Gene Expression Involving Hepatic Oxidative Stress in Rat |
title | Induction Effect of Bisphenol A on Gene Expression Involving Hepatic Oxidative Stress in Rat |
title_full | Induction Effect of Bisphenol A on Gene Expression Involving Hepatic Oxidative Stress in Rat |
title_fullStr | Induction Effect of Bisphenol A on Gene Expression Involving Hepatic Oxidative Stress in Rat |
title_full_unstemmed | Induction Effect of Bisphenol A on Gene Expression Involving Hepatic Oxidative Stress in Rat |
title_short | Induction Effect of Bisphenol A on Gene Expression Involving Hepatic Oxidative Stress in Rat |
title_sort | induction effect of bisphenol a on gene expression involving hepatic oxidative stress in rat |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4842055/ https://www.ncbi.nlm.nih.gov/pubmed/27143994 http://dx.doi.org/10.1155/2016/6298515 |
work_keys_str_mv | AT kazemisohrab inductioneffectofbisphenolaongeneexpressioninvolvinghepaticoxidativestressinrat AT mousaviseydehnarges inductioneffectofbisphenolaongeneexpressioninvolvinghepaticoxidativestressinrat AT aghapourfahimeh inductioneffectofbisphenolaongeneexpressioninvolvinghepaticoxidativestressinrat AT rezaeeboshra inductioneffectofbisphenolaongeneexpressioninvolvinghepaticoxidativestressinrat AT sadeghifarzin inductioneffectofbisphenolaongeneexpressioninvolvinghepaticoxidativestressinrat AT moghadamniaaliakbar inductioneffectofbisphenolaongeneexpressioninvolvinghepaticoxidativestressinrat |