Neuroprotection for traumatic brain injury: translational challenges and emerging therapeutic strategies

被引:445
作者
Loane, David J.
Faden, Alan I. [1 ]
机构
[1] Univ Maryland, Sch Med, Natl Study Ctr Trauma & Emergency Med Syst, Dept Anesthesiol, Baltimore, MD 21201 USA
基金
美国国家卫生研究院;
关键词
POLY(ADP-RIBOSE) POLYMERASE INHIBITOR; ACUTE MITOCHONDRIAL DYSFUNCTION; CYCLOSPORINE-A; CELL-CYCLE; INTERLEUKIN-1; RECEPTOR; FUNCTIONAL DEFICITS; CORTICAL CONTUSION; CLINICAL-TRIALS; NEURONAL DEATH; REDUCES INFLAMMATION;
D O I
10.1016/j.tips.2010.09.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Traumatic brain injury (TBI) causes secondary biochemical changes that contribute to subsequent tissue damage and associated neuronal cell death. Neuroprotective treatments that limit secondary tissue loss and/or improve behavioral outcome have been well established in multiple animal models of TBI. However, translation of such neuroprotective strategies to human injury have been disappointing, with the failure of more than thirty controlled clinical trials. Both conceptual issues and methodological differences between preclinical and clinical injury have undoubtedly contributed to these translational difficulties. More recently, changes in experimental approach, as well as altered clinical trial methodologies, have raised cautious optimism regarding the outcomes of future clinical trials. Here we critically review developing experimental neuroprotective strategies that show promise, and we propose criteria for improving the probability of successful clinical translation.
引用
收藏
页码:596 / 604
页数:9
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