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Neuronal Cells Rearrangement During Aging and Neurodegenerative Disease: Metabolism, Oxidative Stress and Organelles Dynamic

Brain cells normally respond adaptively to oxidative stress or bioenergetic challenges, resulting from ongoing activity in neuronal circuits. During aging and in neurodegenerative disorders, these mechanisms are compromised. In fact, neurons show unique age-related changes in functions and metabolis...

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Autores principales: Castelli, Vanessa, Benedetti, Elisabetta, Antonosante, Andrea, Catanesi, Mariano, Pitari, Giuseppina, Ippoliti, Rodolfo, Cimini, Annamaria, d’Angelo, Michele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6546816/
https://www.ncbi.nlm.nih.gov/pubmed/31191244
http://dx.doi.org/10.3389/fnmol.2019.00132
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author Castelli, Vanessa
Benedetti, Elisabetta
Antonosante, Andrea
Catanesi, Mariano
Pitari, Giuseppina
Ippoliti, Rodolfo
Cimini, Annamaria
d’Angelo, Michele
author_facet Castelli, Vanessa
Benedetti, Elisabetta
Antonosante, Andrea
Catanesi, Mariano
Pitari, Giuseppina
Ippoliti, Rodolfo
Cimini, Annamaria
d’Angelo, Michele
author_sort Castelli, Vanessa
collection PubMed
description Brain cells normally respond adaptively to oxidative stress or bioenergetic challenges, resulting from ongoing activity in neuronal circuits. During aging and in neurodegenerative disorders, these mechanisms are compromised. In fact, neurons show unique age-related changes in functions and metabolism, resulting in greater susceptibility to insults and disease. Aging affects the nervous system as well as other organs. More precisely, as the nervous system ages, neuron metabolism may change, inducing glucose hypometabolism, impaired transport of critical substrates underlying metabolism, alterations in calcium signaling, and mitochondrial dysfunction. Moreover, in neuronal aging, an accumulation of impaired and aggregated proteins in the cytoplasm and in mitochondria is observed, as the result of oxidative stress: reduced antioxidant defenses and/or increase of reactive oxygen species (ROS). These changes lead to greater vulnerability of neurons in various regions of the brain and increased susceptibility to several diseases. Specifically, the first part of the review article will focus on the major neuronal cells’ rearrangements during aging in response to changes in metabolism and oxidative stress, while the second part will cover the neurodegenerative disease areas in detail.
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spelling pubmed-65468162019-06-12 Neuronal Cells Rearrangement During Aging and Neurodegenerative Disease: Metabolism, Oxidative Stress and Organelles Dynamic Castelli, Vanessa Benedetti, Elisabetta Antonosante, Andrea Catanesi, Mariano Pitari, Giuseppina Ippoliti, Rodolfo Cimini, Annamaria d’Angelo, Michele Front Mol Neurosci Neuroscience Brain cells normally respond adaptively to oxidative stress or bioenergetic challenges, resulting from ongoing activity in neuronal circuits. During aging and in neurodegenerative disorders, these mechanisms are compromised. In fact, neurons show unique age-related changes in functions and metabolism, resulting in greater susceptibility to insults and disease. Aging affects the nervous system as well as other organs. More precisely, as the nervous system ages, neuron metabolism may change, inducing glucose hypometabolism, impaired transport of critical substrates underlying metabolism, alterations in calcium signaling, and mitochondrial dysfunction. Moreover, in neuronal aging, an accumulation of impaired and aggregated proteins in the cytoplasm and in mitochondria is observed, as the result of oxidative stress: reduced antioxidant defenses and/or increase of reactive oxygen species (ROS). These changes lead to greater vulnerability of neurons in various regions of the brain and increased susceptibility to several diseases. Specifically, the first part of the review article will focus on the major neuronal cells’ rearrangements during aging in response to changes in metabolism and oxidative stress, while the second part will cover the neurodegenerative disease areas in detail. Frontiers Media S.A. 2019-05-28 /pmc/articles/PMC6546816/ /pubmed/31191244 http://dx.doi.org/10.3389/fnmol.2019.00132 Text en Copyright © 2019 Castelli, Benedetti, Antonosante, Catanesi, Pitari, Ippoliti, Cimini and d’Angelo. 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
Castelli, Vanessa
Benedetti, Elisabetta
Antonosante, Andrea
Catanesi, Mariano
Pitari, Giuseppina
Ippoliti, Rodolfo
Cimini, Annamaria
d’Angelo, Michele
Neuronal Cells Rearrangement During Aging and Neurodegenerative Disease: Metabolism, Oxidative Stress and Organelles Dynamic
title Neuronal Cells Rearrangement During Aging and Neurodegenerative Disease: Metabolism, Oxidative Stress and Organelles Dynamic
title_full Neuronal Cells Rearrangement During Aging and Neurodegenerative Disease: Metabolism, Oxidative Stress and Organelles Dynamic
title_fullStr Neuronal Cells Rearrangement During Aging and Neurodegenerative Disease: Metabolism, Oxidative Stress and Organelles Dynamic
title_full_unstemmed Neuronal Cells Rearrangement During Aging and Neurodegenerative Disease: Metabolism, Oxidative Stress and Organelles Dynamic
title_short Neuronal Cells Rearrangement During Aging and Neurodegenerative Disease: Metabolism, Oxidative Stress and Organelles Dynamic
title_sort neuronal cells rearrangement during aging and neurodegenerative disease: metabolism, oxidative stress and organelles dynamic
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6546816/
https://www.ncbi.nlm.nih.gov/pubmed/31191244
http://dx.doi.org/10.3389/fnmol.2019.00132
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