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Assessment of metals induced histopathological and gene expression changes in different organs of non-diabetic and diabetic rats

Diabetes is a complex metabolic disorder and different environmental toxicants including heavy metals have been involved in diabetes induction. Therefore, assessment of the environmental risk factors and heavy metals induced toxicity have become critical for reducing the consequences of metals pollu...

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Autores principales: Riaz, Muhammad Ahsan, Nisa, Zaib Un, Anjum, Muhammad Sohail, Butt, Hira, Mehmood, Azra, Riaz, Ayesha, Akhtar, Amtul Bari Tabinda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7125094/
https://www.ncbi.nlm.nih.gov/pubmed/32246071
http://dx.doi.org/10.1038/s41598-020-62807-0
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author Riaz, Muhammad Ahsan
Nisa, Zaib Un
Anjum, Muhammad Sohail
Butt, Hira
Mehmood, Azra
Riaz, Ayesha
Akhtar, Amtul Bari Tabinda
author_facet Riaz, Muhammad Ahsan
Nisa, Zaib Un
Anjum, Muhammad Sohail
Butt, Hira
Mehmood, Azra
Riaz, Ayesha
Akhtar, Amtul Bari Tabinda
author_sort Riaz, Muhammad Ahsan
collection PubMed
description Diabetes is a complex metabolic disorder and different environmental toxicants including heavy metals have been involved in diabetes induction. Therefore, assessment of the environmental risk factors and heavy metals induced toxicity have become critical for reducing the consequences of metals pollutants. Previously, we reported heavy metals induced nephrotoxicity in non-diabetic and diabetic rats. Here, we extended our analysis by examining the heavy metals induced organs (heart, kidney, liver, pancreas, and spleen) damage in diabetic and non-diabetic Wistar rats using histopathology and quantitative real-time PCR (qRT-PCR). Following the generation of the diabetic rat model, the animals were exposed to heavy metals including lead (Pb), arsenic (As), manganese (Mn) and cadmium (Cd). Both non-diabetic and diabetic rats were exposed to heavy metals for 30 days and subsequently, the heart, kidney, liver, pancreas and spleen tissues were examined. Heavy metal treatment resulted in irregularly arranged myofibrils and vacuolization in the heart tissue of metal treated groups as evident from hematoxylin and eosin (H & E) staining. The kidney tissue of rats treated with heavy metals showed tubular degeneration, fibrosis, hemorrhage, and vacuolation. The liver of the heavy metals treated rats exhibited cellular degeneration and necrosis. The pancreatic tissue of streptozotocin injected untreated and metal treated rats revealed severe degeneration, necrosis, degranulation, shrinkage, and depression in the islets of Langerhans. Increased red pulp area and congestion were observed in the spleen of the metal mixture treated non-diabetic and diabetic rats. In line with the histological data, the qRT-PCR analysis showed downregulated expression of Bcl(2) and upregulation of Caspase-3 in non-diabetic and diabetic metal treated rats as compared to the non-diabetic untreated rats. In conclusion, the present study revealed, diabetic rats are more prone to metal alone as well as metal mixture induced organ damage as compared to non-diabetic rats.
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spelling pubmed-71250942020-04-08 Assessment of metals induced histopathological and gene expression changes in different organs of non-diabetic and diabetic rats Riaz, Muhammad Ahsan Nisa, Zaib Un Anjum, Muhammad Sohail Butt, Hira Mehmood, Azra Riaz, Ayesha Akhtar, Amtul Bari Tabinda Sci Rep Article Diabetes is a complex metabolic disorder and different environmental toxicants including heavy metals have been involved in diabetes induction. Therefore, assessment of the environmental risk factors and heavy metals induced toxicity have become critical for reducing the consequences of metals pollutants. Previously, we reported heavy metals induced nephrotoxicity in non-diabetic and diabetic rats. Here, we extended our analysis by examining the heavy metals induced organs (heart, kidney, liver, pancreas, and spleen) damage in diabetic and non-diabetic Wistar rats using histopathology and quantitative real-time PCR (qRT-PCR). Following the generation of the diabetic rat model, the animals were exposed to heavy metals including lead (Pb), arsenic (As), manganese (Mn) and cadmium (Cd). Both non-diabetic and diabetic rats were exposed to heavy metals for 30 days and subsequently, the heart, kidney, liver, pancreas and spleen tissues were examined. Heavy metal treatment resulted in irregularly arranged myofibrils and vacuolization in the heart tissue of metal treated groups as evident from hematoxylin and eosin (H & E) staining. The kidney tissue of rats treated with heavy metals showed tubular degeneration, fibrosis, hemorrhage, and vacuolation. The liver of the heavy metals treated rats exhibited cellular degeneration and necrosis. The pancreatic tissue of streptozotocin injected untreated and metal treated rats revealed severe degeneration, necrosis, degranulation, shrinkage, and depression in the islets of Langerhans. Increased red pulp area and congestion were observed in the spleen of the metal mixture treated non-diabetic and diabetic rats. In line with the histological data, the qRT-PCR analysis showed downregulated expression of Bcl(2) and upregulation of Caspase-3 in non-diabetic and diabetic metal treated rats as compared to the non-diabetic untreated rats. In conclusion, the present study revealed, diabetic rats are more prone to metal alone as well as metal mixture induced organ damage as compared to non-diabetic rats. Nature Publishing Group UK 2020-04-03 /pmc/articles/PMC7125094/ /pubmed/32246071 http://dx.doi.org/10.1038/s41598-020-62807-0 Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Riaz, Muhammad Ahsan
Nisa, Zaib Un
Anjum, Muhammad Sohail
Butt, Hira
Mehmood, Azra
Riaz, Ayesha
Akhtar, Amtul Bari Tabinda
Assessment of metals induced histopathological and gene expression changes in different organs of non-diabetic and diabetic rats
title Assessment of metals induced histopathological and gene expression changes in different organs of non-diabetic and diabetic rats
title_full Assessment of metals induced histopathological and gene expression changes in different organs of non-diabetic and diabetic rats
title_fullStr Assessment of metals induced histopathological and gene expression changes in different organs of non-diabetic and diabetic rats
title_full_unstemmed Assessment of metals induced histopathological and gene expression changes in different organs of non-diabetic and diabetic rats
title_short Assessment of metals induced histopathological and gene expression changes in different organs of non-diabetic and diabetic rats
title_sort assessment of metals induced histopathological and gene expression changes in different organs of non-diabetic and diabetic rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7125094/
https://www.ncbi.nlm.nih.gov/pubmed/32246071
http://dx.doi.org/10.1038/s41598-020-62807-0
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