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Mechanisms of Modulation of Ferroptosis and Its Role in Central Nervous System Diseases
Ferroptosis is a new form of programmed cell death characterized by intracellular iron-dependent accumulation of lipid peroxide and primarily associated with iron metabolism, glutathione-dependent pathway, and coenzyme Q(10)-dependent pathway. Recent studies demonstrate that ferroptosis is associate...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8213017/ https://www.ncbi.nlm.nih.gov/pubmed/34149412 http://dx.doi.org/10.3389/fphar.2021.657033 |
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author | Tan, Qingyun Fang, Yuying Gu, Qiong |
author_facet | Tan, Qingyun Fang, Yuying Gu, Qiong |
author_sort | Tan, Qingyun |
collection | PubMed |
description | Ferroptosis is a new form of programmed cell death characterized by intracellular iron-dependent accumulation of lipid peroxide and primarily associated with iron metabolism, glutathione-dependent pathway, and coenzyme Q(10)-dependent pathway. Recent studies demonstrate that ferroptosis is associated with central nervous system (CNS) diseases, such as stroke, Parkinson’s disease, Alzheimer’s disease, and Huntington’s disease. This review summarizes the key regulatory mechanisms of ferroptosis and its role in CNS diseases. These updates may provide novel perspective for the development of therapeutical agents against CNS diseases. |
format | Online Article Text |
id | pubmed-8213017 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82130172021-06-19 Mechanisms of Modulation of Ferroptosis and Its Role in Central Nervous System Diseases Tan, Qingyun Fang, Yuying Gu, Qiong Front Pharmacol Pharmacology Ferroptosis is a new form of programmed cell death characterized by intracellular iron-dependent accumulation of lipid peroxide and primarily associated with iron metabolism, glutathione-dependent pathway, and coenzyme Q(10)-dependent pathway. Recent studies demonstrate that ferroptosis is associated with central nervous system (CNS) diseases, such as stroke, Parkinson’s disease, Alzheimer’s disease, and Huntington’s disease. This review summarizes the key regulatory mechanisms of ferroptosis and its role in CNS diseases. These updates may provide novel perspective for the development of therapeutical agents against CNS diseases. Frontiers Media S.A. 2021-06-04 /pmc/articles/PMC8213017/ /pubmed/34149412 http://dx.doi.org/10.3389/fphar.2021.657033 Text en Copyright © 2021 Tan, Fang and Gu. 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 | Pharmacology Tan, Qingyun Fang, Yuying Gu, Qiong Mechanisms of Modulation of Ferroptosis and Its Role in Central Nervous System Diseases |
title | Mechanisms of Modulation of Ferroptosis and Its Role in Central Nervous System Diseases |
title_full | Mechanisms of Modulation of Ferroptosis and Its Role in Central Nervous System Diseases |
title_fullStr | Mechanisms of Modulation of Ferroptosis and Its Role in Central Nervous System Diseases |
title_full_unstemmed | Mechanisms of Modulation of Ferroptosis and Its Role in Central Nervous System Diseases |
title_short | Mechanisms of Modulation of Ferroptosis and Its Role in Central Nervous System Diseases |
title_sort | mechanisms of modulation of ferroptosis and its role in central nervous system diseases |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8213017/ https://www.ncbi.nlm.nih.gov/pubmed/34149412 http://dx.doi.org/10.3389/fphar.2021.657033 |
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