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Iron and Targeted Iron Therapy in Alzheimer’s Disease

Alzheimer’s disease (AD) is the most common neurodegenerative disease worldwide. β-amyloid plaque (Aβ) deposition and hyperphosphorylated tau, as well as dysregulated energy metabolism in the brain, are key factors in the progression of AD. Many studies have observed abnormal iron accumulation in di...

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Autores principales: Wang, Jian, Fu, Jiaying, Zhao, Yuanxin, Liu, Qingqing, Yan, Xiaoyu, Su, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10671546/
https://www.ncbi.nlm.nih.gov/pubmed/38003544
http://dx.doi.org/10.3390/ijms242216353
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author Wang, Jian
Fu, Jiaying
Zhao, Yuanxin
Liu, Qingqing
Yan, Xiaoyu
Su, Jing
author_facet Wang, Jian
Fu, Jiaying
Zhao, Yuanxin
Liu, Qingqing
Yan, Xiaoyu
Su, Jing
author_sort Wang, Jian
collection PubMed
description Alzheimer’s disease (AD) is the most common neurodegenerative disease worldwide. β-amyloid plaque (Aβ) deposition and hyperphosphorylated tau, as well as dysregulated energy metabolism in the brain, are key factors in the progression of AD. Many studies have observed abnormal iron accumulation in different regions of the AD brain, which is closely correlated with the clinical symptoms of AD; therefore, understanding the role of brain iron accumulation in the major pathological aspects of AD is critical for its treatment. This review discusses the main mechanisms and recent advances in the involvement of iron in the above pathological processes, including in iron-induced oxidative stress-dependent and non-dependent directions, summarizes the hypothesis that the iron-induced dysregulation of energy metabolism may be an initiating factor for AD, based on the available evidence, and further discusses the therapeutic perspectives of targeting iron.
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spelling pubmed-106715462023-11-15 Iron and Targeted Iron Therapy in Alzheimer’s Disease Wang, Jian Fu, Jiaying Zhao, Yuanxin Liu, Qingqing Yan, Xiaoyu Su, Jing Int J Mol Sci Review Alzheimer’s disease (AD) is the most common neurodegenerative disease worldwide. β-amyloid plaque (Aβ) deposition and hyperphosphorylated tau, as well as dysregulated energy metabolism in the brain, are key factors in the progression of AD. Many studies have observed abnormal iron accumulation in different regions of the AD brain, which is closely correlated with the clinical symptoms of AD; therefore, understanding the role of brain iron accumulation in the major pathological aspects of AD is critical for its treatment. This review discusses the main mechanisms and recent advances in the involvement of iron in the above pathological processes, including in iron-induced oxidative stress-dependent and non-dependent directions, summarizes the hypothesis that the iron-induced dysregulation of energy metabolism may be an initiating factor for AD, based on the available evidence, and further discusses the therapeutic perspectives of targeting iron. MDPI 2023-11-15 /pmc/articles/PMC10671546/ /pubmed/38003544 http://dx.doi.org/10.3390/ijms242216353 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Wang, Jian
Fu, Jiaying
Zhao, Yuanxin
Liu, Qingqing
Yan, Xiaoyu
Su, Jing
Iron and Targeted Iron Therapy in Alzheimer’s Disease
title Iron and Targeted Iron Therapy in Alzheimer’s Disease
title_full Iron and Targeted Iron Therapy in Alzheimer’s Disease
title_fullStr Iron and Targeted Iron Therapy in Alzheimer’s Disease
title_full_unstemmed Iron and Targeted Iron Therapy in Alzheimer’s Disease
title_short Iron and Targeted Iron Therapy in Alzheimer’s Disease
title_sort iron and targeted iron therapy in alzheimer’s disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10671546/
https://www.ncbi.nlm.nih.gov/pubmed/38003544
http://dx.doi.org/10.3390/ijms242216353
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