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

机译:颅脑外伤的神经保护:转化挑战和新兴的治疗策略。

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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.
机译:颅脑外伤(TBI)会引起继发性生物化学变化,从而导致随后的组织损伤和相关的神经元细胞死亡。限制继发性组织损失和/或改善行为结果的神经保护性治疗在TBI的多种动物模型中已得到很好的确立。然而,这种神经保护策略对人的伤害的翻译令人失望,超过三十项对照临床试验都失败了。临床前和临床损伤之间的概念问题和方法学差异无疑都导致了这些翻译困难。最近,实验方法的变化以及临床试验方法的变化,使人们对未来临床试验的结果持谨慎的乐观态度。在这里,我们批判性地审查开发实验神经保护策略,显示出希望,并提出提高临床成功翻译可能性的标准。

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