The pathophysiology of repetitive concussive traumatic brain injury in experimental models; new developments and open questions

被引:41
作者
Brody, David L. [1 ]
Benetatos, Joseph
Bennett, Rachel E.
Klemenhagen, Kristen C.
Mac Donald, Christine L.
机构
[1] Washington Univ, Sch Med, Dept Neurol, St Louis, MO 63110 USA
关键词
Concussion; Traumatic brain injury; Traumatic axonal injury; Amyloid-beta; Tau; Microglia; Depression; Social behavior; Mouse; Sertraline; AMYLOID PROTEIN DEPOSITION; AXONAL INJURY; MOUSE MODEL; ALZHEIMERS-DISEASE; DENDRITIC SPINES; TAU OLIGOMERS; COGNITIVE IMPAIRMENT; PRECURSOR PROTEIN; HEAD-INJURY; RAT MODEL;
D O I
10.1016/j.mcn.2015.02.005
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In recent years, there has been an increasing interest in the pathophysiology of repetitive concussive traumatic brain injury (rcTBI) in large part due to the association with dramatic cases of progressive neurological deterioration in professional athletes, military personnel, and others. However, our understanding of the pathophysiology of rcTBI is less advanced than for more severe brain injuries. Most prominently, the mechanisms underlying traumatic axonal injury, microglial activation, amyloid-beta accumulation, and progressive tau pathology are not yet known. In addition, the role of injury to dendritic spine cytoskeletal structures, vascular reactivity impairments, and microthrombi are intriguing and subjects of ongoing inquiry. Methods for quantitative analysis of axonal injury, dendritic injury, and synaptic loss need to be refined for the field to move forward in a rigorous fashion. We and others are attempting to develop translational approaches to assess these specific pathophysiological events in both animals and humans to facilitate clinically relevant pharmacodynamic assessments of candidate therapeutics. In this article, we review and discuss several of the recent experimental results from our lab and others. We include new initial data describing the difficulty in modeling progressive tau pathology in experimental rcTBI, and results demonstrating that sertraline can alleviate social interaction deficits and depressive-like behaviors following experimental rcTBI plus foot shock stress. Furthermore, we propose a discrete set of open, experimentally tractable questions that may serve as a framework for future investigations. In addition, we also raise several important questions that are less experimentally tractable at this time, in hopes that they may stimulate future methodological developments to address them. This article is part of a Special Issue entitled "Traumatic Brain Injury". (C) 2015 Elsevier Inc All rights reserved.
引用
收藏
页码:91 / 98
页数:8
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