Long-Term Consequences of Traumatic Brain Injury: Current Status of Potential Mechanisms of Injury and Neurological Outcomes

被引:343
作者
Bramlett, Helen M. [1 ]
Dietrich, W. Dalton [1 ]
机构
[1] Univ Miami, Miller Sch Med, Dept Neurol Surg, Miami Project Cure Paralysis, Miami, FL 33136 USA
基金
美国国家卫生研究院;
关键词
atrophy; inflammation; neurogenesis; progressive damage; TBI; white matter; CONTROLLED CORTICAL IMPACT; SPINAL-CORD-INJURY; CEREBRAL-BLOOD-FLOW; CALPAIN-MEDIATED PROTEOLYSIS; AMYLOID PRECURSOR PROTEIN; FLUID-PERCUSSION INJURY; CLOSED-HEAD-INJURY; IN-VIVO MODEL; ADULT HIPPOCAMPAL NEUROGENESIS; LATE POSTTRAUMATIC SEIZURES;
D O I
10.1089/neu.2014.3352
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Traumatic brain injury (TBI) is a significant clinical problem with few therapeutic interventions successfully translated to the clinic. Increased importance on the progressive, long-term consequences of TBI have been emphasized, both in the experimental and clinical literature. Thus, there is a need for a better understanding of the chronic consequences of TBI, with the ultimate goal of developing novel therapeutic interventions to treat the devastating consequences of brain injury. In models of mild, moderate, and severe TBI, histopathological and behavioral studies have emphasized the progressive nature of the initial traumatic insult and the involvement of multiple pathophysiological mechanisms, including sustained injury cascades leading to prolonged motor and cognitive deficits. Recently, the increased incidence in age-dependent neurodegenerative diseases in this patient population has also been emphasized. Pathomechanisms felt to be active in the acute and long-term consequences of TBI include excitotoxicity, apoptosis, inflammatory events, seizures, demyelination, white matter pathology, as well as decreased neurogenesis. The current article will review many of these pathophysiological mechanisms that may be important targets for limiting the chronic consequences of TBI.
引用
收藏
页码:1834 / 1848
页数:15
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