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Biochemical and histopathological effects of copper oxide nanoparticles exposure on the bivalve Chambardia rubens (Lamarck, 1819)
Copper nanoparticles are widely incorporated into many applications, including air and liquid filters, wood preservatives, batteries, thermal and electrical conductivity, inks and skin products. Their potential toxicity and environmental fate, however, are poorly studied in the freshwater bivalves....
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Portland Press Ltd.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10196149/ https://www.ncbi.nlm.nih.gov/pubmed/37128859 http://dx.doi.org/10.1042/BSR20222308 |
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author | Morad, Mostafa Hassanein, Taha F. El-khadragy, Manal F. Fehaid, Alaa Habotta, Ola A. Abdel Moneim, Ahmed |
author_facet | Morad, Mostafa Hassanein, Taha F. El-khadragy, Manal F. Fehaid, Alaa Habotta, Ola A. Abdel Moneim, Ahmed |
author_sort | Morad, Mostafa |
collection | PubMed |
description | Copper nanoparticles are widely incorporated into many applications, including air and liquid filters, wood preservatives, batteries, thermal and electrical conductivity, inks and skin products. Their potential toxicity and environmental fate, however, are poorly studied in the freshwater bivalves. The aim of the present study was to evaluate the different effects of copper oxide nanoparticles and ionic copper on the digestive glands and gills of the mussel Chambardia rubens. Mussels were treated with 100 and 1000 µg Cu L(−1) of copper oxide nanoparticles (CuONPs) or ionic copper (Cu(2+)) for 3, 7, and 14 days. The Cu accumulation and markers of oxidative stress in the digestive glands and gills were evaluated. The results show that the digestive gland collected higher levels of the two forms of copper than the gills. Exposure to CuONPs or Cu(2+) induced significant elevations in superoxide dismutase, glutathione peroxidase and lipid peroxidation. Notably, a significant decrease was observed in the glutathione levels after exposure to both copper forms. CuONPs only induced a significant increase in glutathione reductase and glutathione S-transferase. The ionic copper only induced a significant decrease in catalase activities in the gill tissues. Overall, CuONPs and Cu(2+) provoked oxidative stress, and further research is needed to clarify their genotoxic and neurotoxic effects on freshwater mussels and other biota. |
format | Online Article Text |
id | pubmed-10196149 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101961492023-05-20 Biochemical and histopathological effects of copper oxide nanoparticles exposure on the bivalve Chambardia rubens (Lamarck, 1819) Morad, Mostafa Hassanein, Taha F. El-khadragy, Manal F. Fehaid, Alaa Habotta, Ola A. Abdel Moneim, Ahmed Biosci Rep Ecology & Environmental Biochemistry Copper nanoparticles are widely incorporated into many applications, including air and liquid filters, wood preservatives, batteries, thermal and electrical conductivity, inks and skin products. Their potential toxicity and environmental fate, however, are poorly studied in the freshwater bivalves. The aim of the present study was to evaluate the different effects of copper oxide nanoparticles and ionic copper on the digestive glands and gills of the mussel Chambardia rubens. Mussels were treated with 100 and 1000 µg Cu L(−1) of copper oxide nanoparticles (CuONPs) or ionic copper (Cu(2+)) for 3, 7, and 14 days. The Cu accumulation and markers of oxidative stress in the digestive glands and gills were evaluated. The results show that the digestive gland collected higher levels of the two forms of copper than the gills. Exposure to CuONPs or Cu(2+) induced significant elevations in superoxide dismutase, glutathione peroxidase and lipid peroxidation. Notably, a significant decrease was observed in the glutathione levels after exposure to both copper forms. CuONPs only induced a significant increase in glutathione reductase and glutathione S-transferase. The ionic copper only induced a significant decrease in catalase activities in the gill tissues. Overall, CuONPs and Cu(2+) provoked oxidative stress, and further research is needed to clarify their genotoxic and neurotoxic effects on freshwater mussels and other biota. Portland Press Ltd. 2023-05-18 /pmc/articles/PMC10196149/ /pubmed/37128859 http://dx.doi.org/10.1042/BSR20222308 Text en © 2023 The Author(s). https://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Ecology & Environmental Biochemistry Morad, Mostafa Hassanein, Taha F. El-khadragy, Manal F. Fehaid, Alaa Habotta, Ola A. Abdel Moneim, Ahmed Biochemical and histopathological effects of copper oxide nanoparticles exposure on the bivalve Chambardia rubens (Lamarck, 1819) |
title | Biochemical and histopathological effects of copper oxide nanoparticles exposure on the bivalve Chambardia rubens (Lamarck, 1819) |
title_full | Biochemical and histopathological effects of copper oxide nanoparticles exposure on the bivalve Chambardia rubens (Lamarck, 1819) |
title_fullStr | Biochemical and histopathological effects of copper oxide nanoparticles exposure on the bivalve Chambardia rubens (Lamarck, 1819) |
title_full_unstemmed | Biochemical and histopathological effects of copper oxide nanoparticles exposure on the bivalve Chambardia rubens (Lamarck, 1819) |
title_short | Biochemical and histopathological effects of copper oxide nanoparticles exposure on the bivalve Chambardia rubens (Lamarck, 1819) |
title_sort | biochemical and histopathological effects of copper oxide nanoparticles exposure on the bivalve chambardia rubens (lamarck, 1819) |
topic | Ecology & Environmental Biochemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10196149/ https://www.ncbi.nlm.nih.gov/pubmed/37128859 http://dx.doi.org/10.1042/BSR20222308 |
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