PLASTICITY IN THE DEVELOPING BRAIN: IMPLICATIONS FOR REHABILITATION

被引:358
作者
Johnston, Michael V. [1 ,2 ,3 ,4 ]
机构
[1] Kennedy Krieger Inst, Dept Neurol, Baltimore, MD 21205 USA
[2] Kennedy Krieger Inst, Dept Pediat, Baltimore, MD 21205 USA
[3] Kennedy Krieger Inst, Dept Phys Med & Rehabil, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
关键词
plasticity; long-term potentiation; synapse; constraint; BDNF glutamate; INDUCED MOVEMENT THERAPY; HUMAN MOTOR CORTEX; EXPERIENCE-DEPENDENT PLASTICITY; RANDOMIZED CONTROLLED-TRIAL; BDNF VAL66MET POLYMORPHISM; HEMIPLEGIC CEREBRAL-PALSY; CROSS-MODAL PLASTICITY; CORTICAL REORGANIZATION; SYNAPTIC PLASTICITY; NERVOUS-SYSTEM;
D O I
10.1002/ddrr.64
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Neuronal plasticity allows the central nervous system to learn skills and remember information, to reorganize neuronal networks in response to environmental stimulation, and to recover from brain and spinal cord injuries. Neuronal plasticity is enhanced in the developing brain and it is usually adaptive and beneficial but can also be maladaptive and responsible for neurological disorders in some situations. Basic mechanisms that are involved in plasticity include neurogenesis, programmed cell death, and activity-dependent synaptic plasticity. Repetitive stimulation of synapses can cause long-term potentiation or long-term depression of neurotransmission. These changes are associated with physical changes in dendritic spines and neuronal circuits. Overproduction of synapses during postnatal development in children contributes to enhanced plasticity by providing an excess of synapses that are pruned during early adolescence. Clinical examples of adaptive neuronal plasticity include reorganization of cortical maps of the fingers in response to practice playing a stringed instrument and constraint-induced movement therapy to improve hemiparesis caused by stroke or cerebral palsy. These forms of plasticity are associated with structural and functional changes in the brain that can be detected with magnetic resonance imaging, positron emission tomography, or transcranial magnetic stimulation (TMS). TMS and other forms of brain stimulation are also being used experimentally to enhance brain plasticity and recovery of function. Plasticity is also influenced by genetic factors such as mutations in brain-derived neuronal growth factor. Understanding brain plasticity provides a basis for developing better therapies to improve outcome from acquired brain injuries. (C) 2009 Wiley-Liss, Inc. Dev Disabil Res Rev 2009;15:94-101.
引用
收藏
页码:94 / 101
页数:8
相关论文
共 87 条
[81]   Mechanisms of enhancement of human motor cortex excitability induced by interventional paired associative stimulation [J].
Stefan, K ;
Kunesch, E ;
Benecke, R ;
Cohen, LG ;
Classen, J .
JOURNAL OF PHYSIOLOGY-LONDON, 2002, 543 (02) :699-708
[82]   Neurons born in the adult dentate gyrus form functional synapses with target cells [J].
Toni, Nicolas ;
Laplagne, Diego A. ;
Zhao, Chunmei ;
Lombardi, Gabriela ;
Ribak, Charles E. ;
Gage, Fred H. ;
Schinder, Alejandro F. .
NATURE NEUROSCIENCE, 2008, 11 (08) :901-907
[83]   Long-term in vivo imaging of experience-dependent synaptic plasticity in adult cortex [J].
Trachtenberg, JT ;
Chen, BE ;
Knott, GW ;
Feng, GP ;
Sanes, JR ;
Welker, E ;
Svoboda, K .
NATURE, 2002, 420 (6917) :788-794
[84]   Increased cortical excitability induced by transcranial DC and peripheral nerve stimulation [J].
Uy, J ;
Ridding, MC .
JOURNAL OF NEUROSCIENCE METHODS, 2003, 127 (02) :193-197
[85]   Constraint-induced therapy in stroke: Magnetic-stimulation motor maps and cerebral activation [J].
Wittenberg, GF ;
Chen, R ;
Ishii, K ;
Bushara, KO ;
Taub, E ;
Gerber, LH ;
Hallett, M ;
Cohen, LG .
NEUROREHABILITATION AND NEURAL REPAIR, 2003, 17 (01) :48-57
[86]  
Wolf SL, 2007, RESTOR NEUROL NEUROS, V25, P549
[87]   Sustained neocortical neurogenesis after neonatal hypoxic/ischemic injury [J].
Yang, Zhengang ;
Covey, Matthew V. ;
Bitel, Claudine L. ;
Ni, Li ;
Jonakait, G. Miller ;
Levison, Steven W. .
ANNALS OF NEUROLOGY, 2007, 61 (03) :199-208