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Salivary gland dysfunction and salivary redox imbalance in patients with Alzheimer’s disease
Alzheimer’s disease (AD) is associated with the deposition of β-amyloid in the brain. AD accounts for over 50% of cases of dementia which results from disturbances in redox homeostasis. Indeed, increased intensity of protein oxidation and nitration as well as lipid peroxidation is observed in brain...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8668975/ https://www.ncbi.nlm.nih.gov/pubmed/34903846 http://dx.doi.org/10.1038/s41598-021-03456-9 |
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author | Zalewska, Anna Klimiuk, Anna Zięba, Sara Wnorowska, Olga Rusak, Małgorzata Waszkiewicz, Napoleon Szarmach, Izabela Dzierżanowski, Krzysztof Maciejczyk, Mateusz |
author_facet | Zalewska, Anna Klimiuk, Anna Zięba, Sara Wnorowska, Olga Rusak, Małgorzata Waszkiewicz, Napoleon Szarmach, Izabela Dzierżanowski, Krzysztof Maciejczyk, Mateusz |
author_sort | Zalewska, Anna |
collection | PubMed |
description | Alzheimer’s disease (AD) is associated with the deposition of β-amyloid in the brain. AD accounts for over 50% of cases of dementia which results from disturbances in redox homeostasis. Indeed, increased intensity of protein oxidation and nitration as well as lipid peroxidation is observed in brain areas with considerable amounts of amyloid plaques and neurofibrillary tangles. However, little is known about the oxidoreductive balance of salivary glands in AD patients. Therefore, the aim of this study was to evaluate the antioxidant barrier and oxidative/nitrosative stress biomarkers in stimulated saliva and blood of AD patients. The study was participated by 25 AD patients and 25 non-demented controls without neurological diseases or cognitive impairment, matched by age and gender to the study group. The number of patients was determined based on a previous pilot study (test power = 0.9). We found a significant decrease in the activity of erythrocyte superoxide dismutase (SOD) and glutathione peroxidase (GPx), increased activity of catalase (CAT) and reduced concentration of plasma non-enzymatic antioxidants (uric acid, UA and reduced glutathione, GSH). In contrast, in the stimulated saliva of AD patients we observed significantly decreased activity of all antioxidant enzymes (SOD, CAT and GPx) as well as concentration of GSH compared to the control group. The content of lipid (malondialdehyde, MDA) and protein (advanced oxidation protein products, AOPP; advanced glycation end-products, AGE) oxidation products as well as biomarkers of nitrosative stress (peroxynitrite, nitrotyrosine) was significantly higher in both saliva and plasma of AD patients compared to the controls. In AD patients, we also observed a considerable decrease in stimulated saliva secretion and salivary total protein content, and an increase in salivary β-amyloid concentration. In conclusion, AD results in redox imbalance towards oxidative reactions, both at the level of the oral cavity and the entire body. General redox balance disturbances do not coincide with salivary redox balance disturbances. Reduction in stimulated saliva secretion in AD patients reflects secretory dysfunction of the parotid glands. |
format | Online Article Text |
id | pubmed-8668975 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-86689752021-12-15 Salivary gland dysfunction and salivary redox imbalance in patients with Alzheimer’s disease Zalewska, Anna Klimiuk, Anna Zięba, Sara Wnorowska, Olga Rusak, Małgorzata Waszkiewicz, Napoleon Szarmach, Izabela Dzierżanowski, Krzysztof Maciejczyk, Mateusz Sci Rep Article Alzheimer’s disease (AD) is associated with the deposition of β-amyloid in the brain. AD accounts for over 50% of cases of dementia which results from disturbances in redox homeostasis. Indeed, increased intensity of protein oxidation and nitration as well as lipid peroxidation is observed in brain areas with considerable amounts of amyloid plaques and neurofibrillary tangles. However, little is known about the oxidoreductive balance of salivary glands in AD patients. Therefore, the aim of this study was to evaluate the antioxidant barrier and oxidative/nitrosative stress biomarkers in stimulated saliva and blood of AD patients. The study was participated by 25 AD patients and 25 non-demented controls without neurological diseases or cognitive impairment, matched by age and gender to the study group. The number of patients was determined based on a previous pilot study (test power = 0.9). We found a significant decrease in the activity of erythrocyte superoxide dismutase (SOD) and glutathione peroxidase (GPx), increased activity of catalase (CAT) and reduced concentration of plasma non-enzymatic antioxidants (uric acid, UA and reduced glutathione, GSH). In contrast, in the stimulated saliva of AD patients we observed significantly decreased activity of all antioxidant enzymes (SOD, CAT and GPx) as well as concentration of GSH compared to the control group. The content of lipid (malondialdehyde, MDA) and protein (advanced oxidation protein products, AOPP; advanced glycation end-products, AGE) oxidation products as well as biomarkers of nitrosative stress (peroxynitrite, nitrotyrosine) was significantly higher in both saliva and plasma of AD patients compared to the controls. In AD patients, we also observed a considerable decrease in stimulated saliva secretion and salivary total protein content, and an increase in salivary β-amyloid concentration. In conclusion, AD results in redox imbalance towards oxidative reactions, both at the level of the oral cavity and the entire body. General redox balance disturbances do not coincide with salivary redox balance disturbances. Reduction in stimulated saliva secretion in AD patients reflects secretory dysfunction of the parotid glands. Nature Publishing Group UK 2021-12-13 /pmc/articles/PMC8668975/ /pubmed/34903846 http://dx.doi.org/10.1038/s41598-021-03456-9 Text en © The Author(s) 2021 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 Zalewska, Anna Klimiuk, Anna Zięba, Sara Wnorowska, Olga Rusak, Małgorzata Waszkiewicz, Napoleon Szarmach, Izabela Dzierżanowski, Krzysztof Maciejczyk, Mateusz Salivary gland dysfunction and salivary redox imbalance in patients with Alzheimer’s disease |
title | Salivary gland dysfunction and salivary redox imbalance in patients with Alzheimer’s disease |
title_full | Salivary gland dysfunction and salivary redox imbalance in patients with Alzheimer’s disease |
title_fullStr | Salivary gland dysfunction and salivary redox imbalance in patients with Alzheimer’s disease |
title_full_unstemmed | Salivary gland dysfunction and salivary redox imbalance in patients with Alzheimer’s disease |
title_short | Salivary gland dysfunction and salivary redox imbalance in patients with Alzheimer’s disease |
title_sort | salivary gland dysfunction and salivary redox imbalance in patients with alzheimer’s disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8668975/ https://www.ncbi.nlm.nih.gov/pubmed/34903846 http://dx.doi.org/10.1038/s41598-021-03456-9 |
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