Brandt Jaclyn, Evans Jonathan T, Mildenhall Taylor, Mulligan Amanda, Konieczny Aimee, Rose Samuel J, English Arthur W
Department of Cell Biology, Emory University School of Medicine, Atlanta, Georgia.
Department of Cell Biology, Emory University School of Medicine, Atlanta, Georgia
J Neurophysiol. 2015 Apr 1;113(7):2390-9. doi: 10.1152/jn.00892.2014. Epub 2015 Jan 28.
Transection of a peripheral nerve results in withdrawal of synapses from motoneurons. Some of the withdrawn synapses are restored spontaneously, but those containing the vesicular glutamate transporter 1 (VGLUT1), and arising mainly from primary afferent neurons, are withdrawn permanently. If animals are exercised immediately after nerve injury, regeneration of the damaged axons is enhanced and no withdrawal of synapses from injured motoneurons can be detected. We investigated whether delaying the onset of exercise until after synapse withdrawal had occurred would yield similar results. In Lewis rats, the right sciatic nerve was cut and repaired. Reinnervation of the soleus muscle was monitored until a direct muscle (M) response was observed to stimulation of the tibial nerve. At that time, rats began 2 wk of daily treadmill exercise using an interval training protocol. Both M responses and electrically-evoked H reflexes were monitored weekly for an additional seven wk. Contacts made by structures containing VGLUT1 or glutamic acid decarboxylase (GAD67) with motoneurons were studied from confocal images of retrogradely labeled cells. Timing of full muscle reinnervation was similar in both delayed and immediately exercised rats. H reflex amplitude in delayed exercised rats was only half that found in immediately exercised animals. Unlike immediately exercised animals, motoneuron contacts containing VGLUT1 in delayed exercised rats were reduced significantly, relative to intact rats. The therapeutic window for application of exercise as a treatment to promote restoration of synaptic inputs onto motoneurons following peripheral nerve injury is different from that for promoting axon regeneration in the periphery.
外周神经横断会导致运动神经元的突触撤回。一些撤回的突触会自发恢复,但那些含有囊泡谷氨酸转运体1(VGLUT1)且主要来自初级传入神经元的突触会被永久撤回。如果动物在神经损伤后立即进行运动,受损轴突的再生会增强,并且未检测到受伤运动神经元的突触撤回。我们研究了将运动开始时间推迟到突触撤回发生之后是否会产生类似的结果。在Lewis大鼠中,切断右侧坐骨神经并进行修复。监测比目鱼肌的再支配情况,直到观察到对胫神经刺激的直接肌肉(M)反应。此时,大鼠开始使用间歇训练方案进行为期2周的每日跑步机运动。在接下来的7周内每周监测M反应和电诱发的H反射。从逆行标记细胞的共聚焦图像研究含有VGLUT1或谷氨酸脱羧酶(GAD67)的结构与运动神经元的接触情况。延迟运动和立即运动的大鼠中完全肌肉再支配的时间相似。延迟运动大鼠的H反射幅度仅为立即运动动物的一半。与立即运动的动物不同,延迟运动大鼠中含有VGLUT1的运动神经元接触相对于完整大鼠显著减少。运动作为促进外周神经损伤后运动神经元突触输入恢复的治疗方法的治疗窗口与促进外周轴突再生的治疗窗口不同。