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Modeling chronic traumatic encephalopathy: the way forward for future discovery
被引:16
|作者:
Turner, Ryan C.
[1
,2
]
Lucke-Wold, Brandon P.
[1
,2
]
Logsdon, Aric F.
[2
,3
]
Robson, Matthew J.
[4
]
Lee, John M.
[5
]
Bailes, Julian E.
[6
]
Dashnaw, Matthew L.
[7
]
Huber, Jason D.
[2
,3
]
Petraglia, Anthony L.
[8
]
Rosen, Charles L.
[1
,2
]
机构:
[1] W Virginia Univ, Sch Med, Dept Neurosurg, Morgantown, WV 26506 USA
[2] W Virginia Univ, Sch Med, Ctr Neurosci, Morgantown, WV 26506 USA
[3] W Virginia Univ, Sch Pharm, Dept Basic Pharmaceut Sci, Morgantown, WV 26506 USA
[4] Vanderbilt Univ, Sch Med, Dept Pharmacol, Nashville, TN 37235 USA
[5] Univ Chicago, Pritzker Sch Med, NorthShore Univ Hlth Syst, Dept Pathol & Lab Med, Evanston, IL USA
[6] Univ Chicago, Pritzker Sch Med, NorthShore Univ Hlth Syst, Dept Neurosurg, Evanston, IL USA
[7] Univ Rochester, Sch Med & Dent, Dept Neurosurg, Rochester, NY USA
[8] Rochester Reg Hlth, Div Neurosurg, Rochester, NY USA
来源:
FRONTIERS IN NEUROLOGY
|
2015年
/
6卷
关键词:
chronic traumatic encephalopathy;
preclinical models;
neurodegeneration;
hyperphosphorylated tau;
neurotrauma;
CONTROLLED CORTICAL IMPACT;
MILD BRAIN-INJURY;
IN-VITRO MODEL;
COGNITIVE IMPAIRMENT;
ALZHEIMERS-DISEASE;
AXONAL INJURY;
MOUSE MODEL;
HEAD-INJURY;
ENHANCES NEUROGENESIS;
DOCOSAHEXAENOIC ACID;
D O I:
10.3389/fneur.2015.00223
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Despite the extensive media coverage associated with the diagnosis of chronic traumatic encephalopathy (CTE), our fundamental understanding of the disease pathophysiology remains in its infancy. Only recently have scientific laboratories and personnel begun to explore CTE pathophysiology through the use of preclinical models of neurotrauma. Some studies have shown the ability to recapitulate some aspects of CTE in rodent models, through the use of various neuropathological, biochemical, and/or behavioral assays. Many questions related to CTE development, however, remain unanswered. These include the role of impact severity, the time interval between impacts, the age at which impacts occur, and the total number of impacts sustained. Other important variables such as the location of impacts, character of impacts, and effect of environment/lifestyle and genetics also warrant further study. In this work, we attempt to address some of these questions by exploring work previously completed using single- and repetitive-injury paradigms. Despite some models producing some deficits similar to CTE symptoms, it is clear that further studies are required to understand the development of neuropathological and neurobehavioral features consistent with CTE-like features in rodents. Specifically, acute and chronic studies are needed that characterize the development of tau-based pathology.
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页数:18
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