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创伤性脑损伤在一种已知表现出延迟性沃勒氏变性的突变小鼠品系中会导致延迟性运动和认知障碍。

Traumatic brain injury causes delayed motor and cognitive impairment in a mutant mouse strain known to exhibit delayed Wallerian degeneration.

作者信息

Fox G B, Faden A I

机构信息

Georgetown Institute for Cognitive and Computational Sciences, Georgetown University Medical Center, Washington, DC 20007-2197, USA.

出版信息

J Neurosci Res. 1998 Sep 15;53(6):718-27. doi: 10.1002/(SICI)1097-4547(19980915)53:6<718::AID-JNR9>3.0.CO;2-8.

Abstract

Delayed Wallerian degeneration after neuronal injury is a feature of the C57BL/Wld(s) mouse mutant. In the present study, we examined the effect of unilateral controlled cortical impact (CCI) on motor and cognitive performance in C57BL/6 and C57BL/Wld(s) mice. Performance on a beam-walking task was impaired in both injured groups over the first 3 weeks; however, between 28 and 35 days post injury, C57BL/6 mice continued to improve whereas C57BL/Wld(s) mice showed increased footfaults. In a spatial learning task, C57BL/Wld(s) animals performed consistently better than C57BL/6 mice when tested 7-10 days and 14-17 days following CCI. C57BL/Wld(s) mice also demonstrated improved working memory performance as compared with C57BL/6 mice when trained on days 21-22 after injury; this effect was lost on days 23 and 24, and was not evident in other animals tested in the same task at 28-31 days following injury. These results indicate a marked delay in motor and cognitive impairment following CCI in C57BL/Wld(s) mice compared with injured C57BL/6 controls. This is consistent with previous work showing delayed temporal evolution of neuronal degeneration in C57BL/Wld(s) mice and suggests CCI may be a suitable model for examining the functional consequences of traumatic brain injury (TBI) in genetically altered mice.

摘要

神经元损伤后出现的延迟性沃勒变性是C57BL/Wld(s)小鼠突变体的一个特征。在本研究中,我们检测了单侧控制性皮质撞击(CCI)对C57BL/6和C57BL/Wld(s)小鼠运动和认知能力的影响。在最初3周内,两个损伤组在走平衡木任务中的表现均受损;然而,在损伤后28至35天之间,C57BL/6小鼠持续改善,而C57BL/Wld(s)小鼠的失足次数增加。在空间学习任务中,在CCI后7 - 10天和14 - 17天进行测试时,C57BL/Wld(s)动物的表现始终优于C57BL/6小鼠。与C57BL/6小鼠相比,在损伤后第21 - 22天进行训练时,C57BL/Wld(s)小鼠的工作记忆表现也有所改善;这种效果在第23天和第24天消失,并且在损伤后28 - 31天在同一任务中测试的其他动物中不明显。这些结果表明,与受伤的C57BL/6对照小鼠相比,C57BL/Wld(s)小鼠在CCI后运动和认知障碍出现明显延迟。这与之前的研究结果一致,即C57BL/Wld(s)小鼠中神经元变性的时间演变延迟,表明CCI可能是研究基因改变小鼠创伤性脑损伤(TBI)功能后果的合适模型。

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