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Vicious cycle of lipid peroxidation and iron accumulation in neurodegeneration

Lipid peroxidation and iron accumulation are closely associated with neurodegenerative diseases, such as Alzheimer’s, Parkinson’s, and Huntington’s diseases, or neurodegeneration with brain iron accumulation disorders. Mitochondrial dysfunction, lipofuscin accumulation, autophagy disruption, and fer...

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Autores principales: Villalón-García, Irene, Povea-Cabello, Suleva, Álvarez-Córdoba, Mónica, Talaverón-Rey, Marta, Suárez-Rivero, Juan M., Suárez-Carrillo, Alejandra, Munuera-Cabeza, Manuel, Reche-López, Diana, Cilleros-Holgado, Paula, Piñero-Pérez, Rocío, Sánchez-Alcázar, José A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9838166/
https://www.ncbi.nlm.nih.gov/pubmed/36453394
http://dx.doi.org/10.4103/1673-5374.358614
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author Villalón-García, Irene
Povea-Cabello, Suleva
Álvarez-Córdoba, Mónica
Talaverón-Rey, Marta
Suárez-Rivero, Juan M.
Suárez-Carrillo, Alejandra
Munuera-Cabeza, Manuel
Reche-López, Diana
Cilleros-Holgado, Paula
Piñero-Pérez, Rocío
Sánchez-Alcázar, José A.
author_facet Villalón-García, Irene
Povea-Cabello, Suleva
Álvarez-Córdoba, Mónica
Talaverón-Rey, Marta
Suárez-Rivero, Juan M.
Suárez-Carrillo, Alejandra
Munuera-Cabeza, Manuel
Reche-López, Diana
Cilleros-Holgado, Paula
Piñero-Pérez, Rocío
Sánchez-Alcázar, José A.
author_sort Villalón-García, Irene
collection PubMed
description Lipid peroxidation and iron accumulation are closely associated with neurodegenerative diseases, such as Alzheimer’s, Parkinson’s, and Huntington’s diseases, or neurodegeneration with brain iron accumulation disorders. Mitochondrial dysfunction, lipofuscin accumulation, autophagy disruption, and ferroptosis have been implicated as the critical pathomechanisms of lipid peroxidation and iron accumulation in these disorders. Currently, the connection between lipid peroxidation and iron accumulation and the initial cause or consequence in neurodegeneration processes is unclear. In this review, we have compiled the known mechanisms by which lipid peroxidation triggers iron accumulation and lipofuscin formation, and the effect of iron overload on lipid peroxidation and cellular function. The vicious cycle established between both pathological alterations may lead to the development of neurodegeneration. Therefore, the investigation of these mechanisms is essential for exploring therapeutic strategies to restrict neurodegeneration. In addition, we discuss the interplay between lipid peroxidation and iron accumulation in neurodegeneration, particularly in PLA2G6-associated neurodegeneration, a rare neurodegenerative disease with autosomal recessive inheritance, which belongs to the group of neurodegeneration with brain iron accumulation disorders.
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spelling pubmed-98381662023-01-14 Vicious cycle of lipid peroxidation and iron accumulation in neurodegeneration Villalón-García, Irene Povea-Cabello, Suleva Álvarez-Córdoba, Mónica Talaverón-Rey, Marta Suárez-Rivero, Juan M. Suárez-Carrillo, Alejandra Munuera-Cabeza, Manuel Reche-López, Diana Cilleros-Holgado, Paula Piñero-Pérez, Rocío Sánchez-Alcázar, José A. Neural Regen Res Review Lipid peroxidation and iron accumulation are closely associated with neurodegenerative diseases, such as Alzheimer’s, Parkinson’s, and Huntington’s diseases, or neurodegeneration with brain iron accumulation disorders. Mitochondrial dysfunction, lipofuscin accumulation, autophagy disruption, and ferroptosis have been implicated as the critical pathomechanisms of lipid peroxidation and iron accumulation in these disorders. Currently, the connection between lipid peroxidation and iron accumulation and the initial cause or consequence in neurodegeneration processes is unclear. In this review, we have compiled the known mechanisms by which lipid peroxidation triggers iron accumulation and lipofuscin formation, and the effect of iron overload on lipid peroxidation and cellular function. The vicious cycle established between both pathological alterations may lead to the development of neurodegeneration. Therefore, the investigation of these mechanisms is essential for exploring therapeutic strategies to restrict neurodegeneration. In addition, we discuss the interplay between lipid peroxidation and iron accumulation in neurodegeneration, particularly in PLA2G6-associated neurodegeneration, a rare neurodegenerative disease with autosomal recessive inheritance, which belongs to the group of neurodegeneration with brain iron accumulation disorders. Wolters Kluwer - Medknow 2022-10-24 /pmc/articles/PMC9838166/ /pubmed/36453394 http://dx.doi.org/10.4103/1673-5374.358614 Text en Copyright: © Neural Regeneration Research https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Review
Villalón-García, Irene
Povea-Cabello, Suleva
Álvarez-Córdoba, Mónica
Talaverón-Rey, Marta
Suárez-Rivero, Juan M.
Suárez-Carrillo, Alejandra
Munuera-Cabeza, Manuel
Reche-López, Diana
Cilleros-Holgado, Paula
Piñero-Pérez, Rocío
Sánchez-Alcázar, José A.
Vicious cycle of lipid peroxidation and iron accumulation in neurodegeneration
title Vicious cycle of lipid peroxidation and iron accumulation in neurodegeneration
title_full Vicious cycle of lipid peroxidation and iron accumulation in neurodegeneration
title_fullStr Vicious cycle of lipid peroxidation and iron accumulation in neurodegeneration
title_full_unstemmed Vicious cycle of lipid peroxidation and iron accumulation in neurodegeneration
title_short Vicious cycle of lipid peroxidation and iron accumulation in neurodegeneration
title_sort vicious cycle of lipid peroxidation and iron accumulation in neurodegeneration
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9838166/
https://www.ncbi.nlm.nih.gov/pubmed/36453394
http://dx.doi.org/10.4103/1673-5374.358614
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