Plasticity and injury in the developing brain

被引:147
作者
Johnston, Michael V. [1 ,2 ,3 ]
Ishida, Akira [4 ]
Ishida, Wako Nakajima [5 ]
Matsushita, Hiroko Baber [6 ]
Nishimura, Akira [7 ]
Tsuji, Masahiro [8 ]
机构
[1] Kennedy Krieger Inst, Dept Neurol, Baltimore, MD 21205 USA
[2] Kennedy Krieger Inst, Dept Pediat, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Baltimore, MD 21205 USA
[4] Ishida Pediat Clin, Akita, Japan
[5] Akita Univ, Sch Med, Dept Pediat, Akita 010, Japan
[6] Kyoto City Hosp, Dept Pediat, Kyoto, Japan
[7] Kyoto Prefectural Univ Med, Dept Pediat, Kyoto 602, Japan
[8] Gen Hosp, Kobe City Med Ctr, Dept Pediat, Kobe, Hyogo, Japan
关键词
Plasticity; Injury; Fragile X syndrome; Rett syndrome; Hypoxia ischemia; NMDA; AMPA; Periventricular leukomalacia; LONG-TERM POTENTIATION; X MENTAL-RETARDATION; NEONATAL HYPOXIA-ISCHEMIA; METABOTROPIC GLUTAMATE RECEPTORS; FRAGILE-X; SYNAPTIC PLASTICITY; MOUSE MODEL; RETT-SYNDROME; NITRIC-OXIDE; CELL-DEATH;
D O I
10.1016/j.braindev.2008.03.014
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The child's brain is more malleable or plastic than that of adults and this accounts for the ability of children to learn new skills quickly or recovery from brain injuries. Several mechanisms contribute to this ability including overproduction and deletion of neurons and synapses, and activity-dependent stabilization of synapses. The molecular mechanisms for activity-dependent synaptic plasticity are being discovered and this is leading to a better understanding of the pathogenesis of several disorders including neurofibromatosis, tuberous sclerosis, Fragile X syndrome and Rett syndrome. Many or the same pathways involved in synaptic plasticity, such as glutamate-mediated excitation, can also mediate brain injury when the brain is exposed to stress or energy failure such as hypoxia ischemia. Recent evidence indicates that cell death pathways activated by injury differ between males and females, This new information about the molecular pathways involved in brain plasticity and injury are leading to insights that will provide better therapies for pediatric neurological disorders. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 10
页数:10
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