Reactive Oxygen Species in the Regulation of Synaptic Plasticity and Memory

被引:445
作者
Massaad, Cynthia A. [1 ]
Klann, Eric [2 ]
机构
[1] Baylor Coll Med, Dept Mol Physiol & Biophys, Houston, TX 77030 USA
[2] NYU, Ctr Neural Sci, New York, NY 10003 USA
关键词
LONG-TERM POTENTIATION; ALPHA-LIPOIC-ACID; NITRIC-OXIDE SYNTHASE; PROTEIN-KINASE-C; MANGANESE SUPEROXIDE-DISMUTASE; TRAUMATIC BRAIN-INJURY; FREE-RADICAL SCAVENGER; AMYLOID PRECURSOR PROTEIN; CENTRAL-NERVOUS-SYSTEM; CHRONIC GRANULOMATOUS-DISEASE;
D O I
10.1089/ars.2010.3208
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The brain is a metabolically active organ exhibiting high oxygen consumption and robust production of reactive oxygen species (ROS). The large amounts of ROS are kept in check by an elaborate network of antioxidants, which sometimes fail and lead to neuronal oxidative stress. Thus, ROS are typically categorized as neurotoxic molecules and typically exert their detrimental effects via oxidation of essential macromolecules such as enzymes and cytoskeletal proteins. Most importantly, excessive ROS are associated with decreased performance in cognitive function. However, at physiological concentrations, ROS are involved in functional changes necessary for synaptic plasticity and hence, for normal cognitive function. The fine line of role reversal of ROS from good molecules to bad molecules is far from being fully understood. This review focuses on identifying the multiple sources of ROS in the mammalian nervous system and on presenting evidence for the critical and essential role of ROS in synaptic plasticity and memory. The review also shows that the inability to restrain either age-or pathology-related increases in ROS levels leads to opposite, detrimental effects that are involved in impairments in synaptic plasticity and memory function. Antioxid. Redox Signal. 14, 2013-2054.
引用
收藏
页码:2013 / 2054
页数:42
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