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Peripheral metabolic alterations associated with pathological manifestations of Parkinson’s disease in gut-brain axis-based mouse model
INTRODUCTION: Parkinson’s disease (PD) is a representative neurodegenerative disease, and its diagnosis relies on the evaluation of clinical manifestations or brain neuroimaging in the absence of a crucial noninvasive biomarker. Here, we used non-targeted metabolomics profiling to identify metabolic...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10447900/ https://www.ncbi.nlm.nih.gov/pubmed/37635904 http://dx.doi.org/10.3389/fnmol.2023.1201073 |
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author | Huh, Eugene Choi, Jin Gyu Lee, Mee Youn Kim, Jin Hee Choi, Yujin Ju, In Gyoung Eo, Hyeyoon Park, Myoung Gyu Kim, Dong-Hyun Park, Hi-Joon Lee, Choong Hwan Oh, Myung Sook |
author_facet | Huh, Eugene Choi, Jin Gyu Lee, Mee Youn Kim, Jin Hee Choi, Yujin Ju, In Gyoung Eo, Hyeyoon Park, Myoung Gyu Kim, Dong-Hyun Park, Hi-Joon Lee, Choong Hwan Oh, Myung Sook |
author_sort | Huh, Eugene |
collection | PubMed |
description | INTRODUCTION: Parkinson’s disease (PD) is a representative neurodegenerative disease, and its diagnosis relies on the evaluation of clinical manifestations or brain neuroimaging in the absence of a crucial noninvasive biomarker. Here, we used non-targeted metabolomics profiling to identify metabolic alterations in the colon and plasma samples of Proteus mirabilis (P. mirabilis)-treated mice, which is a possible animal model for investigating the microbiota-gut-brain axis. METHODS: We performed gas chromatography–mass spectrometry to analyze the samples and detected metabolites that could reflect P. mirabilis-induced disease progression and pathology. RESULTS AND DISCUSSION: Pattern, correlation and pathway enrichment analyses showed significant alterations in sugar metabolism such as galactose metabolism and fructose and mannose metabolism, which are closely associated with energy metabolism and lipid metabolism. This study indicates possible metabolic factors for P. mirabilis-induced pathological progression and provides evidence of metabolic alterations associated with P. mirabilis-mediated pathology of brain neurodegeneration. |
format | Online Article Text |
id | pubmed-10447900 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-104479002023-08-25 Peripheral metabolic alterations associated with pathological manifestations of Parkinson’s disease in gut-brain axis-based mouse model Huh, Eugene Choi, Jin Gyu Lee, Mee Youn Kim, Jin Hee Choi, Yujin Ju, In Gyoung Eo, Hyeyoon Park, Myoung Gyu Kim, Dong-Hyun Park, Hi-Joon Lee, Choong Hwan Oh, Myung Sook Front Mol Neurosci Molecular Neuroscience INTRODUCTION: Parkinson’s disease (PD) is a representative neurodegenerative disease, and its diagnosis relies on the evaluation of clinical manifestations or brain neuroimaging in the absence of a crucial noninvasive biomarker. Here, we used non-targeted metabolomics profiling to identify metabolic alterations in the colon and plasma samples of Proteus mirabilis (P. mirabilis)-treated mice, which is a possible animal model for investigating the microbiota-gut-brain axis. METHODS: We performed gas chromatography–mass spectrometry to analyze the samples and detected metabolites that could reflect P. mirabilis-induced disease progression and pathology. RESULTS AND DISCUSSION: Pattern, correlation and pathway enrichment analyses showed significant alterations in sugar metabolism such as galactose metabolism and fructose and mannose metabolism, which are closely associated with energy metabolism and lipid metabolism. This study indicates possible metabolic factors for P. mirabilis-induced pathological progression and provides evidence of metabolic alterations associated with P. mirabilis-mediated pathology of brain neurodegeneration. Frontiers Media S.A. 2023-08-10 /pmc/articles/PMC10447900/ /pubmed/37635904 http://dx.doi.org/10.3389/fnmol.2023.1201073 Text en Copyright © 2023 Huh, Choi, Lee, Kim, Choi, Ju, Eo, Park, Kim, Park, Lee and Oh. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Molecular Neuroscience Huh, Eugene Choi, Jin Gyu Lee, Mee Youn Kim, Jin Hee Choi, Yujin Ju, In Gyoung Eo, Hyeyoon Park, Myoung Gyu Kim, Dong-Hyun Park, Hi-Joon Lee, Choong Hwan Oh, Myung Sook Peripheral metabolic alterations associated with pathological manifestations of Parkinson’s disease in gut-brain axis-based mouse model |
title | Peripheral metabolic alterations associated with pathological manifestations of Parkinson’s disease in gut-brain axis-based mouse model |
title_full | Peripheral metabolic alterations associated with pathological manifestations of Parkinson’s disease in gut-brain axis-based mouse model |
title_fullStr | Peripheral metabolic alterations associated with pathological manifestations of Parkinson’s disease in gut-brain axis-based mouse model |
title_full_unstemmed | Peripheral metabolic alterations associated with pathological manifestations of Parkinson’s disease in gut-brain axis-based mouse model |
title_short | Peripheral metabolic alterations associated with pathological manifestations of Parkinson’s disease in gut-brain axis-based mouse model |
title_sort | peripheral metabolic alterations associated with pathological manifestations of parkinson’s disease in gut-brain axis-based mouse model |
topic | Molecular Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10447900/ https://www.ncbi.nlm.nih.gov/pubmed/37635904 http://dx.doi.org/10.3389/fnmol.2023.1201073 |
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