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Activity cage as a method to analyze functional recovery after sciatic nerve injury in mice

机译:活动笼作为一种分析小鼠坐骨神经损伤后功能恢复的方法

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The aim of this paper is to show the activity cage as a viable method for tracking functional nerve recovery. The activity cage measures spontaneous coordinate activity, meaning movement in either the horizontal or vertical plane, of experimental animals within a specified amount of time. This uses a minimum of researcher time conducting functional testing to determine functional recovery of the nerve. Using microsurgical forceps, a crush injury was inflicted unilaterally, on the left side, upon the 4-month-old C3H mice creating a very high. degree of pressure for 6 s upon the exposed sciatic nerve. The locomotion function of the mice was evaluated using the activity cage preoperatively, 1, 7, 14, 21, and 28 days after the surgical procedure. We found that using the activity cage functional recovery occurred by 14 days after nerve crush injury. It was also shown that, coinciding with functional recovery, immunohistochemistry changes for GD1a and nNOS appeared at the level of L4, where the sciatic nerve joins the spinal column. GD1a and nNOS have both been linked to regenerative processes in mammalian nervous systems.
机译:本文的目的是展示活动笼,作为追踪功能性神经恢复的可行方法。活动笼测量自发的坐标活动,即在指定的时间内在实验动物的水平或垂直平面上的运动。这花费了最少的研究人员时间来进行功能测试,以确定神经的功能恢复。使用显微外科手术钳,在4个月大的C3H小鼠身上产生了非常高的伤害,左侧单侧造成了挤压伤。坐骨神经暴露6秒。在手术后1、7、14、21和28天,使用活动笼评估小鼠的运动功能。我们发现使用活动笼可以在神经挤压伤后14天发生功能恢复。还显示,与功能恢复一致,GD1a和nNOS的免疫组织化学变化出现在坐骨神经连接脊柱的L4水平。 GD1a和nNOS都与哺乳动物神经系统的再生过程有关。

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