Texas Biomedical Device Center, The University of Texas at Dallas, 800 West Campbell Road, Richardson, TX, 75080-3021, USA.
School of Behavioral and Brain Sciences, The University of Texas at Dallas, 800 West Campbell Road, Richardson, TX, 75080-3021, USA.
Nat Commun. 2019 Dec 19;10(1):5782. doi: 10.1038/s41467-019-13695-0.
Nerve damage can cause chronic, debilitating problems including loss of motor control and paresthesia, and generates maladaptive neuroplasticity as central networks attempt to compensate for the loss of peripheral connectivity. However, it remains unclear if this is a critical feature responsible for the expression of symptoms. Here, we use brief bursts of closed-loop vagus nerve stimulation (CL-VNS) delivered during rehabilitation to reverse the aberrant central plasticity resulting from forelimb nerve transection. CL-VNS therapy drives extensive synaptic reorganization in central networks paralleled by improved sensorimotor recovery without any observable changes in the nerve or muscle. Depleting cortical acetylcholine blocks the plasticity-enhancing effects of CL-VNS and consequently eliminates recovery, indicating a critical role for brain circuits in recovery. These findings demonstrate that manipulations to enhance central plasticity can improve sensorimotor recovery and define CL-VNS as a readily translatable therapy to restore function after nerve damage.
神经损伤会导致慢性、使人虚弱的问题,包括运动控制丧失和感觉异常,并产生适应不良的神经可塑性,因为中枢网络试图弥补外周连接的丧失。然而,目前尚不清楚这是否是导致症状表达的关键特征。在这里,我们在康复过程中使用短暂的闭环迷走神经刺激(CL-VNS)来逆转前肢神经切断引起的异常中枢可塑性。CL-VNS 治疗驱动中枢网络中广泛的突触重组,伴随着感觉运动恢复的改善,而神经或肌肉没有任何可见的变化。皮质乙酰胆碱耗竭会阻断 CL-VNS 的可塑性增强作用,从而消除恢复,表明大脑回路在恢复中起着关键作用。这些发现表明,增强中枢可塑性的操作可以改善感觉运动恢复,并将 CL-VNS 定义为一种易于转化的治疗方法,可在神经损伤后恢复功能。