Huber Kathleen B G, Uteshev Victor V, Pauly James R
Department of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, Lexington, KY 40536, USA.
Curr Pharm Des. 2016;22(14):2072-82. doi: 10.2174/1381612822666160127113631.
Development of novel pharmacotherapies for the treatment of traumatic injury to the nervous system has been ongoing for over 40 years. Despite many promising compounds discovered using animal models, no treatments have successfully translated into the clinic. The central dogma in this field is that brain trauma initiates a complex chain of biochemical events leading to secondary brain damage and sustained neurological deficits. The delayed secondary brain injury is likely to result from multiple insults including oxidative stress, mitochondrial dysfunction, breakdown of the blood brain barrier, dysregulated release of glutamate, pro-inflammatory cytokines, and other mediators. However, therapies targeting these systems have generally met with failure in clinical trials. The purpose of this review is to summarize the models used for preclinical neurotrauma research, provide a brief overview of previous failed clinical trials in head and spinal cord injury, and finally, to review involvement of the cholinergic system and discuss implications for future research. Possibilities and pitfalls of targeting the cholinergic system for neuroprotection and/or enhancement of functional recovery are also discussed.
用于治疗神经系统创伤性损伤的新型药物疗法的研发已经进行了40多年。尽管使用动物模型发现了许多有前景的化合物,但没有一种治疗方法成功转化到临床应用。该领域的核心观点是,脑外伤引发一系列复杂的生化事件,导致继发性脑损伤和持续性神经功能缺损。延迟性继发性脑损伤可能是由多种损伤引起的,包括氧化应激、线粒体功能障碍、血脑屏障破坏、谷氨酸、促炎细胞因子和其他介质的释放失调。然而,针对这些系统的疗法在临床试验中通常都失败了。本综述的目的是总结用于临床前神经创伤研究的模型,简要概述先前在头部和脊髓损伤临床试验中失败的情况,最后,回顾胆碱能系统的参与情况并讨论对未来研究的启示。还讨论了针对胆碱能系统进行神经保护和/或促进功能恢复的可能性和陷阱。