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Metabolic Dysregulation Contributes to the Progression of Alzheimer’s Disease
Alzheimer’s disease (AD) is an incurable neurodegenerative disease. Numerous studies have demonstrated a critical role for dysregulated glucose metabolism in its pathogenesis. In this review, we summarize metabolic alterations in aging brain and AD-related metabolic deficits associated with glucose...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7674854/ https://www.ncbi.nlm.nih.gov/pubmed/33250703 http://dx.doi.org/10.3389/fnins.2020.530219 |
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author | Yan, Xu Hu, Yue Wang, Biyao Wang, Sijian Zhang, Xinwen |
author_facet | Yan, Xu Hu, Yue Wang, Biyao Wang, Sijian Zhang, Xinwen |
author_sort | Yan, Xu |
collection | PubMed |
description | Alzheimer’s disease (AD) is an incurable neurodegenerative disease. Numerous studies have demonstrated a critical role for dysregulated glucose metabolism in its pathogenesis. In this review, we summarize metabolic alterations in aging brain and AD-related metabolic deficits associated with glucose metabolism dysregulation, glycolysis dysfunction, tricarboxylic acid (TCA) cycle, oxidative phosphorylation (OXPHOS) deficits, and pentose phosphate pathway impairment. Additionally, we discuss recent treatment strategies targeting metabolic defects in AD, including their limitations, in an effort to encourage the development of novel therapeutic strategies. |
format | Online Article Text |
id | pubmed-7674854 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-76748542020-11-26 Metabolic Dysregulation Contributes to the Progression of Alzheimer’s Disease Yan, Xu Hu, Yue Wang, Biyao Wang, Sijian Zhang, Xinwen Front Neurosci Neuroscience Alzheimer’s disease (AD) is an incurable neurodegenerative disease. Numerous studies have demonstrated a critical role for dysregulated glucose metabolism in its pathogenesis. In this review, we summarize metabolic alterations in aging brain and AD-related metabolic deficits associated with glucose metabolism dysregulation, glycolysis dysfunction, tricarboxylic acid (TCA) cycle, oxidative phosphorylation (OXPHOS) deficits, and pentose phosphate pathway impairment. Additionally, we discuss recent treatment strategies targeting metabolic defects in AD, including their limitations, in an effort to encourage the development of novel therapeutic strategies. Frontiers Media S.A. 2020-11-05 /pmc/articles/PMC7674854/ /pubmed/33250703 http://dx.doi.org/10.3389/fnins.2020.530219 Text en Copyright © 2020 Yan, Hu, Wang, Wang and Zhang. http://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 | Neuroscience Yan, Xu Hu, Yue Wang, Biyao Wang, Sijian Zhang, Xinwen Metabolic Dysregulation Contributes to the Progression of Alzheimer’s Disease |
title | Metabolic Dysregulation Contributes to the Progression of Alzheimer’s Disease |
title_full | Metabolic Dysregulation Contributes to the Progression of Alzheimer’s Disease |
title_fullStr | Metabolic Dysregulation Contributes to the Progression of Alzheimer’s Disease |
title_full_unstemmed | Metabolic Dysregulation Contributes to the Progression of Alzheimer’s Disease |
title_short | Metabolic Dysregulation Contributes to the Progression of Alzheimer’s Disease |
title_sort | metabolic dysregulation contributes to the progression of alzheimer’s disease |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7674854/ https://www.ncbi.nlm.nih.gov/pubmed/33250703 http://dx.doi.org/10.3389/fnins.2020.530219 |
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