Neurorestorative Treatments for Traumatic Brain Injury

被引:4
作者
Xiong, Ye [1 ]
Mahmood, Asim [1 ]
Chopp, Michael [2 ,3 ]
机构
[1] Henry Ford Hlth Syst, Dept Neurosurg, Detroit, MI 48202 USA
[2] Henry Ford Hlth Syst, Dept Neurol, Detroit, MI 48202 USA
[3] Oakland Univ, Dept Phys, Rochester, MI 48309 USA
关键词
MARROW STROMAL CELLS; ERYTHROPOIETIN ENHANCES NEUROGENESIS; HIPPOCAMPAL CA3 REGION; DENTATE GYRUS; THYMOSIN BETA-4; ANGIOGENESIS; RATS; SIMVASTATIN; INCREASE; STROKE;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Traumatic brain injury (TBI) remains a major cause of death and permanent disability worldwide, especially in children and young adults. A total of 1.5 million people experience head trauma each year in the United States, with an annual economic cost exceeding $56 billion. Unfortunately, almost all Phase III TBI clinical trials have yet to yield a safe and effective neuroprotective treatment, raising questions regarding the use of neuroprotective strategies as the primary therapy for acute brain injuries. Recent preclinical data suggest that neurorestorative strategies that promote angiogenesis (formation of new blood vessels from pre-existing endothelial cells), axonal remodeling (axonal sprouting and pruning), neurogenesis (generation of new neurons) and synaptogenesis (formation of new synapses) provide promising opportunities for the treatment of TBI. This review discusses select cell-based and pharmacological therapies that activate and amplify these endogenous restorative brain plasticity processes to promote both repair and regeneration of injured brain tissue and functional recovery after TBI. [Discovery Medicine 10(54):434-442, November 2010]
引用
收藏
页码:434 / 442
页数:9
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