Association between autophagy and rapid eye movement sleep loss-associated neurodegenerative and patho-physio-behavioral changes

被引:26
作者
Chauhan, Amit Kumar [1 ]
Mallick, Birendra Nath [1 ]
机构
[1] Jawaharlal Nehru Univ, Sch Life Sci, New Delhi 110067, India
关键词
Autophagy Memory formation and loss; Neurodegeneration; Neuronal homeostasis; Noradrenaline (NA); Rapid eye movement sleep (REM sleep) loss; K-ATPASE ACTIVITY; CENTRAL-NERVOUS-SYSTEM; REM-SLEEP; ALPHA-SYNUCLEIN; PARADOXICAL SLEEP; RAT-BRAIN; PARKINSONS-DISEASE; MITOCHONDRIAL DYSFUNCTION; PROTEIN AGGREGATION; MEDIATED INCREASE;
D O I
10.1016/j.sleep.2019.04.019
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Rapid eye movement (REM) sleep is a unique physiological process at least expressed in mammals. Its disturbance affects many psycho-somato-physiological processes including cardio-vascular-respiratory systems, brain excitability, neurogenesis, synaptic pruning, and memory consolidation. While it is altered in most neurodegenerative disorders including Alzheimer's disease (AD), Parkinson's disease (PD) and REM sleep behavior disorder (RBD), the detailed mechanism of inducing such action is unknown. Independent studies have reported that by clearing unwanted, dysfunctional intracellular debris, wastes, etc., autophagy maintains cellular health, integrity, and homeostasis. Abnormality in autophagy causes neuronal dysfunction including death, leading to neurodegenerative disorders. It has also been reported that by modulating noradrenaline (NA) levels, REM sleep maintains neuronal integrity and housekeeping functions of the brain. Using PUBMED, we surveyed the literature and found isolated, independent studies showing that autophagy dysfunction is associated with acute and chronic neurodegenerative and patho-physio-behavioral changes, which are also associated with REM sleep loss. We collated these scattered findings, which strongly support our contention that elevated NA associated with REM sleep loss is likely to affect autophagy in neurons, disturbing neuronal integrity and homeostasis and leading to altered brain functions and associated disorders. (C) 2019 Elsevier B.V. All rights reserved.
引用
收藏
页码:29 / 37
页数:9
相关论文
共 137 条
[21]   WIPI2 Links LC3 Conjugation with PI3P, Autophagosome Formation, and Pathogen Clearance by Recruiting Atg12-5-16L1 [J].
Dooley, Hannah C. ;
Razi, Minoo ;
Polson, Hannah E. J. ;
Girardin, Stephen E. ;
Wilson, Michael I. ;
Tooze, Sharon A. .
MOLECULAR CELL, 2014, 55 (02) :238-252
[22]   PARADOXICAL SLEEP - PROLONGED AUGMENTATION FOLLOWING LEARNING [J].
FISHBEIN, W ;
KASTANIOTIS, C ;
CHATTMAN, D .
BRAIN RESEARCH, 1974, 79 (01) :61-75
[23]   Mitophagy in neurodegeneration and aging [J].
Fivenson, Elayne M. ;
Lautrup, Sofie ;
Sun, Nuo ;
Scheibye-Knudsen, Morten ;
Stevnsner, Tinna ;
Nilsen, Hilde ;
Bohr, Vilhelm A. ;
Fang, Evandro F. .
NEUROCHEMISTRY INTERNATIONAL, 2017, 109 :202-209
[24]  
Gadoth N, 2011, OXID STRESS APPL BAS, P1, DOI 10.1007/978-1-60327-514-9
[25]   Glucocerebrosidase gene variants are accumulated in idiopathic REM sleep behavior disorder [J].
Gamez-Valero, Ana ;
Iranzo, Alex ;
Serradell, Monica ;
Vilas, Dolores ;
Santamaria, Joan ;
Gaig, Caries ;
Alvarez, Ramiro ;
Ariza, Aurelio ;
Tolosa, Eduardo ;
Beyer, Katrin .
PARKINSONISM & RELATED DISORDERS, 2018, 50 :94-98
[26]   The role of glucocerebrosidase in Parkinson disease pathogenesis [J].
Gegg, Matthew E. ;
Schapira, Anthony H. V. .
FEBS JOURNAL, 2018, 285 (19) :3591-3603
[27]   Long-term dendritic spine stability in the adult cortex [J].
Grutzendler, J ;
Kasthuri, N ;
Gan, WB .
NATURE, 2002, 420 (6917) :812-816
[28]   Oxidative stress, mitochondrial damage and neurodegenerative diseases [J].
Guo, Chunyan ;
Sun, Li ;
Chen, Xueping ;
Zhang, Danshen .
NEURAL REGENERATION RESEARCH, 2013, 8 (21) :2003-2014
[29]   Mitochondria Supply Membranes for Autophagosome Biogenesis during Starvation [J].
Hailey, Dale W. ;
Rambold, Angelika S. ;
Satpute-Krishnan, Prasanna ;
Mitra, Kasturi ;
Sougrat, Rachid ;
Kim, Peter K. ;
Lippincott-Schwartz, Jennifer .
CELL, 2010, 141 (04) :656-667
[30]   Suppression of basal autophagy in neural cells causes neurodegenerative disease in mice [J].
Hara, Taichi ;
Nakamura, Kenji ;
Matsui, Makoto ;
Yamamoto, Akitsugu ;
Nakahara, Yohko ;
Suzuki-Migishima, Rika ;
Yokoyama, Minesuke ;
Mishima, Kenji ;
Saito, Ichiro ;
Okano, Hideyuki ;
Mizushima, Noboru .
NATURE, 2006, 441 (7095) :885-889