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Curcumin ameliorated low dose-Bisphenol A induced gastric toxicity in adult albino rats
Bisphenol A (BPA) is one of the most common worldwide chemicals involved in the industry of polycarbonate plastics, medical devices, and pharmaceuticals. Forty three-month-old albino rats were randomly classified into four groups. Group Ӏ received a daily corn oil dose (5 mL/kg/ body weight, BW) thr...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9206026/ https://www.ncbi.nlm.nih.gov/pubmed/35715475 http://dx.doi.org/10.1038/s41598-022-14158-1 |
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author | Ismail, Omnia Ibrahim El-Meligy, Manal Mahmoud Samy |
author_facet | Ismail, Omnia Ibrahim El-Meligy, Manal Mahmoud Samy |
author_sort | Ismail, Omnia Ibrahim |
collection | PubMed |
description | Bisphenol A (BPA) is one of the most common worldwide chemicals involved in the industry of polycarbonate plastics, medical devices, and pharmaceuticals. Forty three-month-old albino rats were randomly classified into four groups. Group Ӏ received a daily corn oil dose (5 mL/kg/ body weight, BW) through a gastric tube for one month, Group ӀӀ received a daily dose of Curcumin (200 mg/kg body weight (B.W.) through a gastric tube for one month, Group ӀӀӀ received a daily dose of BPA (0.5 μg/kg B.W.) through a gastric tube for one month and Group ӀV received concomitant daily doses of Bisphenol A and Curcumin as the regimen described in groups ӀӀ and ӀӀӀ. The rats were sacrificed, and glandular portion of stomach was dissected and processed for light, immunohistochemical and ultrastructural study. BPA induced destructed gastric glands, dilated congested blood vessels, submucosal oedema, decreased PAS-positive reactivity, increased collagen fibres deposition, decrease in the positive BCL2 immunoexpression, increased positive PCNA immunoexpression, reduction in the gastric mucosal height and destructive changes in the enteroendocrine, chief and parietal cells. Curcumin coadministration provoked an obvious improvement in the gastric structure. BPA exposure has toxic effects on the glandular portion of the stomach in rats. Otherwise, Curcumin coadministration has exhibited protective impact on the architecture of the stomach. |
format | Online Article Text |
id | pubmed-9206026 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-92060262022-06-19 Curcumin ameliorated low dose-Bisphenol A induced gastric toxicity in adult albino rats Ismail, Omnia Ibrahim El-Meligy, Manal Mahmoud Samy Sci Rep Article Bisphenol A (BPA) is one of the most common worldwide chemicals involved in the industry of polycarbonate plastics, medical devices, and pharmaceuticals. Forty three-month-old albino rats were randomly classified into four groups. Group Ӏ received a daily corn oil dose (5 mL/kg/ body weight, BW) through a gastric tube for one month, Group ӀӀ received a daily dose of Curcumin (200 mg/kg body weight (B.W.) through a gastric tube for one month, Group ӀӀӀ received a daily dose of BPA (0.5 μg/kg B.W.) through a gastric tube for one month and Group ӀV received concomitant daily doses of Bisphenol A and Curcumin as the regimen described in groups ӀӀ and ӀӀӀ. The rats were sacrificed, and glandular portion of stomach was dissected and processed for light, immunohistochemical and ultrastructural study. BPA induced destructed gastric glands, dilated congested blood vessels, submucosal oedema, decreased PAS-positive reactivity, increased collagen fibres deposition, decrease in the positive BCL2 immunoexpression, increased positive PCNA immunoexpression, reduction in the gastric mucosal height and destructive changes in the enteroendocrine, chief and parietal cells. Curcumin coadministration provoked an obvious improvement in the gastric structure. BPA exposure has toxic effects on the glandular portion of the stomach in rats. Otherwise, Curcumin coadministration has exhibited protective impact on the architecture of the stomach. Nature Publishing Group UK 2022-06-17 /pmc/articles/PMC9206026/ /pubmed/35715475 http://dx.doi.org/10.1038/s41598-022-14158-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Ismail, Omnia Ibrahim El-Meligy, Manal Mahmoud Samy Curcumin ameliorated low dose-Bisphenol A induced gastric toxicity in adult albino rats |
title | Curcumin ameliorated low dose-Bisphenol A induced gastric toxicity in adult albino rats |
title_full | Curcumin ameliorated low dose-Bisphenol A induced gastric toxicity in adult albino rats |
title_fullStr | Curcumin ameliorated low dose-Bisphenol A induced gastric toxicity in adult albino rats |
title_full_unstemmed | Curcumin ameliorated low dose-Bisphenol A induced gastric toxicity in adult albino rats |
title_short | Curcumin ameliorated low dose-Bisphenol A induced gastric toxicity in adult albino rats |
title_sort | curcumin ameliorated low dose-bisphenol a induced gastric toxicity in adult albino rats |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9206026/ https://www.ncbi.nlm.nih.gov/pubmed/35715475 http://dx.doi.org/10.1038/s41598-022-14158-1 |
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