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NMR-based metabolomics of urine in a mouse model of Alzheimer’s disease: identification of oxidative stress biomarkers
Alzheimer’s disease (AD) is the most common cause of neurodegenerative dementia among elderly patients. A biomarker for the disease could make diagnosis easier and more accurate, and accelerate drug discovery. In this study, NMR-based metabolomics analysis in conjunction with multivariate statistics...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
the Society for Free Radical Research Japan
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3593130/ https://www.ncbi.nlm.nih.gov/pubmed/23526113 http://dx.doi.org/10.3164/jcbn.12-118 |
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author | Fukuhara, Kiyoshi Ohno, Akiko Ota, Yosuke Senoo, Yuya Maekawa, Keiko Okuda, Haruhiro Kurihara, Masaaki Okuno, Alato Niida, Shumpei Saito, Yoshiro Takikawa, Osamu |
author_facet | Fukuhara, Kiyoshi Ohno, Akiko Ota, Yosuke Senoo, Yuya Maekawa, Keiko Okuda, Haruhiro Kurihara, Masaaki Okuno, Alato Niida, Shumpei Saito, Yoshiro Takikawa, Osamu |
author_sort | Fukuhara, Kiyoshi |
collection | PubMed |
description | Alzheimer’s disease (AD) is the most common cause of neurodegenerative dementia among elderly patients. A biomarker for the disease could make diagnosis easier and more accurate, and accelerate drug discovery. In this study, NMR-based metabolomics analysis in conjunction with multivariate statistics was applied to examine changes in urinary metabolites in transgenic AD mice expressing mutant tau and β-amyloid precursor protein. These mice showed significant changes in urinary metabolites throughout the progress of the disease. Levels of 3-hydroxykynurenine, homogentisate and allantoin were significantly higher compared to control mice in 4 months (prior to onset of AD symptoms) and reverted to control values by 10 months of age (early/middle stage of AD), which highlights the relevance of oxidative stress to this neurodegenerative disorder even prior the onset of dementia. The level of these changed metabolites at very early period may provide an indication of disease risk at asymptomatic stage. |
format | Online Article Text |
id | pubmed-3593130 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | the Society for Free Radical Research Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-35931302013-03-22 NMR-based metabolomics of urine in a mouse model of Alzheimer’s disease: identification of oxidative stress biomarkers Fukuhara, Kiyoshi Ohno, Akiko Ota, Yosuke Senoo, Yuya Maekawa, Keiko Okuda, Haruhiro Kurihara, Masaaki Okuno, Alato Niida, Shumpei Saito, Yoshiro Takikawa, Osamu J Clin Biochem Nutr Original Article Alzheimer’s disease (AD) is the most common cause of neurodegenerative dementia among elderly patients. A biomarker for the disease could make diagnosis easier and more accurate, and accelerate drug discovery. In this study, NMR-based metabolomics analysis in conjunction with multivariate statistics was applied to examine changes in urinary metabolites in transgenic AD mice expressing mutant tau and β-amyloid precursor protein. These mice showed significant changes in urinary metabolites throughout the progress of the disease. Levels of 3-hydroxykynurenine, homogentisate and allantoin were significantly higher compared to control mice in 4 months (prior to onset of AD symptoms) and reverted to control values by 10 months of age (early/middle stage of AD), which highlights the relevance of oxidative stress to this neurodegenerative disorder even prior the onset of dementia. The level of these changed metabolites at very early period may provide an indication of disease risk at asymptomatic stage. the Society for Free Radical Research Japan 2013-03 2013-03-01 /pmc/articles/PMC3593130/ /pubmed/23526113 http://dx.doi.org/10.3164/jcbn.12-118 Text en Copyright © 2013 JCBN This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Fukuhara, Kiyoshi Ohno, Akiko Ota, Yosuke Senoo, Yuya Maekawa, Keiko Okuda, Haruhiro Kurihara, Masaaki Okuno, Alato Niida, Shumpei Saito, Yoshiro Takikawa, Osamu NMR-based metabolomics of urine in a mouse model of Alzheimer’s disease: identification of oxidative stress biomarkers |
title | NMR-based metabolomics of urine in a mouse model of Alzheimer’s disease: identification of oxidative stress biomarkers |
title_full | NMR-based metabolomics of urine in a mouse model of Alzheimer’s disease: identification of oxidative stress biomarkers |
title_fullStr | NMR-based metabolomics of urine in a mouse model of Alzheimer’s disease: identification of oxidative stress biomarkers |
title_full_unstemmed | NMR-based metabolomics of urine in a mouse model of Alzheimer’s disease: identification of oxidative stress biomarkers |
title_short | NMR-based metabolomics of urine in a mouse model of Alzheimer’s disease: identification of oxidative stress biomarkers |
title_sort | nmr-based metabolomics of urine in a mouse model of alzheimer’s disease: identification of oxidative stress biomarkers |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3593130/ https://www.ncbi.nlm.nih.gov/pubmed/23526113 http://dx.doi.org/10.3164/jcbn.12-118 |
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