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

被引:156
作者
Castelli, Vanessa [1 ]
Benedetti, Elisabetta [1 ]
Antonosante, Andrea [1 ]
Catanesi, Mariano [1 ]
Pitari, Giuseppina [1 ]
Ippoliti, Rodolfo [1 ]
Cimini, Annamaria [1 ,2 ]
d'Angelo, Michele [1 ]
机构
[1] Univ Aquila, Dept Life Hlth & Environm Sci, Abruzzo, Italy
[2] Temple Univ, Dept Biol, Sbarro Inst Canc Res & Mol Med, Philadelphia, PA 19122 USA
关键词
aging; neurodegeneration; energetic metabolism; mitochondrial dysfunction; oxidative stress; ENDOPLASMIC-RETICULUM STRESS; AGE-RELATED-CHANGES; TRANSGENIC MOUSE MODEL; HIPPOCAMPAL SYNAPTIC PLASTICITY; (R)-ALPHA-LIPOIC ACID REVERSES; SPINAL GANGLION NEURONS; MYELINATED NERVE-FIBERS; AMYLOID-BETA PEPTIDE; ALZHEIMERS-DISEASE; COGNITIVE DECLINE;
D O I
10.3389/fnmol.2019.00132
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
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 mitochondria! 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.
引用
收藏
页数:13
相关论文
共 201 条
[1]
Cognitive decline in Parkinson disease [J].
Aarsland, Dag ;
Creese, Byron ;
Politis, Marios ;
Chaudhuri, K. Ray ;
Ffytche, Dominic H. ;
Weintraub, Daniel ;
Ballard, Clive .
NATURE REVIEWS NEUROLOGY, 2017, 13 (04) :217-231
[2]
The role of an astrocytic NADPH oxidase in the neurotoxicity of amyloid beta peptides [J].
Abramov, AY ;
Duchen, MR .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2005, 360 (1464) :2309-2314
[3]
A peroxisomal lon protease and peroxisome degradation by autophagy play key roles in vitality of Hansenula polymorpha cells [J].
Aksam, Eda Bener ;
Koek, Anne ;
Kiel, Jan A. K. W. ;
Jourdan, Stefanie ;
Veenhuis, Marten ;
van der Klei, Ida J. .
AUTOPHAGY, 2007, 3 (02) :96-105
[4]
Mechanisms of Oxidative Glutamate Toxicity: The Glutamate/Cystine Antiporter System xc- as a Neuroprotective Drug Target [J].
Albrecht, Philipp ;
Lewerenz, Jan ;
Dittmer, Sonja ;
Noack, Rebecca ;
Maher, Pamela ;
Methner, Axel .
CNS & NEUROLOGICAL DISORDERS-DRUG TARGETS, 2010, 9 (03) :373-382
[5]
Characterizing cognitive aging in humans with links to animal models [J].
Alexander, Gene E. ;
Ryan, Lee ;
Bowers, Dawn ;
Foster, Thomas C. ;
Bizon, Jennifer L. ;
Geldmacher, David S. ;
Glisky, Elizabeth L. .
FRONTIERS IN AGING NEUROSCIENCE, 2012, 4
[6]
Energy-Efficient Action Potentials in Hippocampal Mossy Fibers [J].
Alle, Henrik ;
Roth, Arnd ;
Geiger, Joerg R. P. .
SCIENCE, 2009, 325 (5946) :1405-1408
[7]
Oxidative Stress in the Progression of Alzheimer Disease in the Frontal Cortex [J].
Ansari, Mubeen A. ;
Scheff, Stephen W. .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2010, 69 (02) :155-167
[8]
Mitochondrial health, the epigenome and healthspan [J].
Aon, Miguel A. ;
Cortassa, Sonia ;
Juhaszova, Magdalena ;
Sollott, Steven J. .
CLINICAL SCIENCE, 2016, 130 (15) :1285-1305
[9]
The neural basis of functional brain imaging signals [J].
Attwell, D ;
Iadecola, C .
TRENDS IN NEUROSCIENCES, 2002, 25 (12) :621-625
[10]
An energy budget for signaling in the grey matter of the brain [J].
Attwell, D ;
Laughlin, SB .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2001, 21 (10) :1133-1145