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Long-Term Cognitive Impairments and Pathological Alterations in a Mouse Model of Repetitive Mild Traumatic Brain Injury

机译:反复轻度颅脑损伤的小鼠模型中的长期认知障碍和病理改变。

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摘要

Mild traumatic brain injury (mTBI, also referred to as concussion) accounts for the majority of all traumatic brain injuries. The consequences of repetitive mTBI have become of particular concern for individuals engaged in certain sports or in military operations. Many mTBI patients suffer long-lasting neurobehavioral impairments. In order to expedite pre-clinical research and therapy development, there is a need for animal models that reflect the long-term cognitive and pathological features seen in patients. In the present study, we developed and characterized a mouse model of repetitive mTBI, induced onto the closed head over the left frontal hemisphere with an electromagnetic stereotaxic impact device. Using GFAP-luciferase bioluminescence reporter mice that provide a readout of astrocyte activation, we observed an increase in bioluminescence relative to the force delivered by the impactor after single impact and cumulative effects of repetitive mTBI. Using the injury parameters established in the reporter mice, we induced a repetitive mTBI in wild-type C57BL/6J mice and characterized the long-term outcome. Animals received repetitive mTBI showed a significant impairment in spatial learning and memory when tested at 2 and 6 months after injury. A robust astrogliosis and increased p-Tau immunoreactivity were observed upon post-mortem pathological examinations. These findings are consistent with the deficits and pathology associated with mTBI in humans and support the use of this model to evaluate potential therapeutic approaches.
机译:轻度创伤性脑损伤(mTBI,也称为脑震荡)占所有创伤性脑损伤的大部分。对于从事某些运动或军事行动的个人而言,重复性mTBI的后果已引起特别关注。许多mTBI患者遭受长期的神经行为损害。为了加快临床前研究和治疗的发展,需要一种能反映患者长期认知和病理特征的动物模型。在本研究中,我们开发并表征了重复性mTBI的小鼠模型,该模型通过电磁立体定位装置感应到左额半球上方的闭合头上。使用提供星形胶质细胞激活读数的GFAP荧光素酶生物发光报告基因小鼠,我们观察到相对于单次撞击和重复mTBI累积效应后撞击器传递的力而言,生物发光增加。使用在报告基因小鼠中建立的损伤参数,我们在野生型C57BL / 6J小鼠中诱导了重复的mTBI,并表征了长期预后。接受重复性mTBI的动物在受伤后2和6个月时进行测试,显示其空间学习和记忆能力显着受损。验尸后病理检查发现有健壮的星形胶质细胞增生和p-Tau免疫反应性增加。这些发现与人类中与mTBI相关的缺陷和病理学相一致,并支持使用该模型评估潜在的治疗方法。

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