Lifelong behavioral and neuropathological consequences of repetitive mild traumatic brain injury

被引:86
|
作者
Mouzon, Benoit C. [1 ,2 ,3 ]
Bachmeier, Corbin [1 ,2 ,3 ]
Ojo, Joseph O. [1 ,2 ]
Acker, Christopher M. [4 ]
Ferguson, Scott [1 ,2 ]
Paris, Daniel [1 ,2 ,3 ]
Ait-Ghezala, Ghania [1 ,2 ,3 ]
Crynen, Gogce [1 ,2 ,3 ]
Davies, Peter [4 ]
Mullan, Michael [1 ]
Stewart, William [5 ,6 ]
Crawford, Fiona [1 ,2 ,3 ]
机构
[1] Roskamp Inst, 2040 Whitfield Ave, Sarasota, FL 34243 USA
[2] James A Haley Vet Hosp, Tampa, FL 33612 USA
[3] Open Univ, Milton Keynes, Bucks, England
[4] Feinstein Inst Med Res, Manhasset, NY USA
[5] Queen Elizabeth Glasgow Univ Hosp, Glasgow, Lanark, Scotland
[6] Univ Glasgow, Glasgow, Lanark, Scotland
来源
关键词
FOOTBALL LEAGUE PLAYERS; MOUSE MODEL; COGNITIVE DYSFUNCTION; HIPPOCAMPAL-LESIONS; RECOGNITION MEMORY; HEAD-INJURY; OBJECT RECOGNITION; SILENT EPIDEMIC; ENCEPHALOPATHY; TAU;
D O I
10.1002/acn3.510
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective Exposure to repetitive concussion, or mild traumatic brain injury (mTBI), has been linked with increased risk of long-term neurodegenerative changes, specifically chronic traumatic encephalopathy (CTE). To date, preclinical studies largely have focused on the immediate aftermath of mTBI, with no literature on the lifelong consequences of mTBI in these models. This study provides the first account of lifelong neurobehavioral and histological consequences of repetitive mTBI providing unique insight into the constellation of evolving and ongoing pathologies with late survival. Methods Male C57BL/6J mice (aged 2-3months) were exposed to either single or repetitive mild TBI or sham procedure. Thereafter, animals were monitored and assessed at 24months post last injury for measures of motor coordination, learning deficits, cognitive function, and anxiety-like behavior prior to euthanasia and preparation of the brains for detailed neuropathological and protein biochemical studies. Results At 24months survival animals exposed to r-mTBI showed clear evidence of learning and working memory impairment with a lack of spatial memory and vestibule-motor vestibulomotor deficits compared to sham animals. Associated with these late behavioral deficits there was evidence of ongoing axonal degeneration and neuroinflammation in subcortical white matter tracts. Notably, these changes were also observed after a single mTBI, albeit to a lesser degree than repetitive mTBI. Interpretation In this context, our current data demonstrate, for the first time, that rather than an acute, time limited event, mild TBI can precipitate a lifelong degenerative process. These data therefore suggest that successful treatment strategies should consider both the acute and chronic nature of mTBI.
引用
收藏
页码:64 / 80
页数:17
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