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Features of the response to subchronic low-dose exposure to copper oxide nanoparticles in rats
Copper is an essential trace element for human health and, at the same time, a major industrial metal widely used both in its elemental form and in compounds. We conducted a dose-dependent assessment of the response of outbred albino male rats to subchronic low-dose exposure to copper oxide nanopart...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10363540/ https://www.ncbi.nlm.nih.gov/pubmed/37482581 http://dx.doi.org/10.1038/s41598-023-38976-z |
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author | Sutunkova, Marina P. Ryabova, Yuliya V. Minigalieva, Ilzira A. Bushueva, Tatiana V. Sakhautdinova, Renata R. Bereza, Ivan A. Shaikhova, Daria R. Amromina, Anna M. Chemezov, Aleksei I. Shelomencev, Ivan G. Amromin, Lev A. Valamina, Irene E. Toropova, Liubov V. |
author_facet | Sutunkova, Marina P. Ryabova, Yuliya V. Minigalieva, Ilzira A. Bushueva, Tatiana V. Sakhautdinova, Renata R. Bereza, Ivan A. Shaikhova, Daria R. Amromina, Anna M. Chemezov, Aleksei I. Shelomencev, Ivan G. Amromin, Lev A. Valamina, Irene E. Toropova, Liubov V. |
author_sort | Sutunkova, Marina P. |
collection | PubMed |
description | Copper is an essential trace element for human health and, at the same time, a major industrial metal widely used both in its elemental form and in compounds. We conducted a dose-dependent assessment of the response of outbred albino male rats to subchronic low-dose exposure to copper oxide nanoparticles administered intraperitoneally at cumulative doses of 18 and 36 mg/kg during 6 weeks to exposure groups 1 and 2, respectively. We observed disorders at different levels of organization of the body in the exposed animals, from molecular to organismal. The observed decrease in the activity of succinate dehydrogenase in nucleated blood cells gave evidence of impaired bioenergetics processes. In view of the results of the metabolomics analysis, we assume mitochondrial damage and contribution of apoptotic processes to the pathology induced by copper poisoning. We also assume neurodegenerative effects based on the assessed morphological parameters of the nervous system, results of behavioral tests, and a decreased level of expression of genes encoding NMDA receptor subunits in the hippocampus. The hepatotoxic effect noted by a number of metabolomics-based, biochemical, and cytological indicators was manifested by the impaired protein-synthesizing function of the liver and enhanced degenerative processes in its cells. We also observed a nephrotoxic effect of nanosized copper oxide with a predominant lesion of proximal kidney tubules. At the same time, both doses tested demonstrated such positive health effects as a statistically significant decrease in the activity of alkaline phosphatase and the nucleated blood cell DNA fragmentation factor. Judging by the changes observed, the cumulative dose of copper oxide nanoparticles of 18 mg/kg body weight administered intraperitoneally approximates the threshold one for rats. The established markers of health impairments may serve as a starting point in the development of techniques of early diagnosis of copper poisoning. |
format | Online Article Text |
id | pubmed-10363540 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-103635402023-07-25 Features of the response to subchronic low-dose exposure to copper oxide nanoparticles in rats Sutunkova, Marina P. Ryabova, Yuliya V. Minigalieva, Ilzira A. Bushueva, Tatiana V. Sakhautdinova, Renata R. Bereza, Ivan A. Shaikhova, Daria R. Amromina, Anna M. Chemezov, Aleksei I. Shelomencev, Ivan G. Amromin, Lev A. Valamina, Irene E. Toropova, Liubov V. Sci Rep Article Copper is an essential trace element for human health and, at the same time, a major industrial metal widely used both in its elemental form and in compounds. We conducted a dose-dependent assessment of the response of outbred albino male rats to subchronic low-dose exposure to copper oxide nanoparticles administered intraperitoneally at cumulative doses of 18 and 36 mg/kg during 6 weeks to exposure groups 1 and 2, respectively. We observed disorders at different levels of organization of the body in the exposed animals, from molecular to organismal. The observed decrease in the activity of succinate dehydrogenase in nucleated blood cells gave evidence of impaired bioenergetics processes. In view of the results of the metabolomics analysis, we assume mitochondrial damage and contribution of apoptotic processes to the pathology induced by copper poisoning. We also assume neurodegenerative effects based on the assessed morphological parameters of the nervous system, results of behavioral tests, and a decreased level of expression of genes encoding NMDA receptor subunits in the hippocampus. The hepatotoxic effect noted by a number of metabolomics-based, biochemical, and cytological indicators was manifested by the impaired protein-synthesizing function of the liver and enhanced degenerative processes in its cells. We also observed a nephrotoxic effect of nanosized copper oxide with a predominant lesion of proximal kidney tubules. At the same time, both doses tested demonstrated such positive health effects as a statistically significant decrease in the activity of alkaline phosphatase and the nucleated blood cell DNA fragmentation factor. Judging by the changes observed, the cumulative dose of copper oxide nanoparticles of 18 mg/kg body weight administered intraperitoneally approximates the threshold one for rats. The established markers of health impairments may serve as a starting point in the development of techniques of early diagnosis of copper poisoning. Nature Publishing Group UK 2023-07-23 /pmc/articles/PMC10363540/ /pubmed/37482581 http://dx.doi.org/10.1038/s41598-023-38976-z Text en © The Author(s) 2023 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 Sutunkova, Marina P. Ryabova, Yuliya V. Minigalieva, Ilzira A. Bushueva, Tatiana V. Sakhautdinova, Renata R. Bereza, Ivan A. Shaikhova, Daria R. Amromina, Anna M. Chemezov, Aleksei I. Shelomencev, Ivan G. Amromin, Lev A. Valamina, Irene E. Toropova, Liubov V. Features of the response to subchronic low-dose exposure to copper oxide nanoparticles in rats |
title | Features of the response to subchronic low-dose exposure to copper oxide nanoparticles in rats |
title_full | Features of the response to subchronic low-dose exposure to copper oxide nanoparticles in rats |
title_fullStr | Features of the response to subchronic low-dose exposure to copper oxide nanoparticles in rats |
title_full_unstemmed | Features of the response to subchronic low-dose exposure to copper oxide nanoparticles in rats |
title_short | Features of the response to subchronic low-dose exposure to copper oxide nanoparticles in rats |
title_sort | features of the response to subchronic low-dose exposure to copper oxide nanoparticles in rats |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10363540/ https://www.ncbi.nlm.nih.gov/pubmed/37482581 http://dx.doi.org/10.1038/s41598-023-38976-z |
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