Texas Biomedical Device Center, Richardson, TX 75080, USA; The University of Texas at Dallas, School of Behavioral Brain Sciences, 800 West Campbell Road, GR 41, Richardson, TX 75080-3021, USA.
Texas Biomedical Device Center, Richardson, TX 75080, USA; The University of Texas at Dallas, School of Behavioral Brain Sciences, 800 West Campbell Road, GR 41, Richardson, TX 75080-3021, USA.
Neuroscience. 2019 May 15;406:290-299. doi: 10.1016/j.neuroscience.2019.03.019. Epub 2019 Mar 21.
Repeatedly pairing a brief train of vagus nerve stimulation (VNS) with an auditory stimulus drives reorganization of primary auditory cortex (A1), and the magnitude of this VNS-dependent plasticity is dependent on the stimulation parameters, including intensity and pulse rate. However, there is currently little data to guide the selection of VNS train durations, an easily adjusted parameter that could influence the effect of VNS-based therapies. Here, we tested the effect of varying the duration of the VNS train on the extent of VNS-dependent cortical plasticity. Rats were exposed to a 9 kHz tone 300 times per day for 20 days. Coincident with tone presentation, groups received trains of 4, 16, or 64 pulses of VNS delivered at 30 Hz, corresponding to train durations of 0.125 s, 0.5 s, and 2.0 s, respectively. High-density microelectrode mapping of A1 revealed that 0.5 s duration VNS trains significantly increased the number of neurons in A1 that responded to tones near the paired tone frequency. Trains lasting 0.125 or 2.0 s failed to alter A1 responses, indicating that both shorter and longer stimulation durations are less effective at enhancing plasticity. A second set of experiments evaluating the effect of delivering 4 or 64 pulses in a fixed 0.5 s VNS train duration paired with tone presentation reveal that both slower and faster stimulation rates are less effective at enhancing plasticity. We incorporated these results with previous findings describing the effect of stimulation parameters on VNS-dependent plasticity and activation of neuromodulatory networks to generate a model of synaptic activation by VNS.
反复将短暂的迷走神经刺激 (VNS) 与听觉刺激配对会驱动初级听觉皮层 (A1) 的重组,而这种 VNS 依赖性可塑性的程度取决于刺激参数,包括强度和脉冲率。然而,目前几乎没有数据可以指导 VNS 刺激串时长的选择,这是一个易于调整的参数,可能会影响基于 VNS 的治疗效果。在这里,我们测试了改变 VNS 刺激串时长对 VNS 依赖性皮质可塑性程度的影响。大鼠每天暴露于 9 kHz 音调 300 次。与音调呈现同时,各组接受以 30 Hz 传递的 4、16 或 64 个脉冲的 VNS 刺激串,分别对应于刺激串时长 0.125 s、0.5 s 和 2.0 s。A1 的高密度微电极映射显示,0.5 s 时长的 VNS 刺激串显著增加了对配对音调附近音调有反应的 A1 神经元数量。持续 0.125 或 2.0 s 的刺激串未能改变 A1 反应,表明较短和较长的刺激持续时间在增强可塑性方面效果较差。第二项实验评估了以固定的 0.5 s VNS 刺激串时长与音调呈现配对的情况下传递 4 或 64 个脉冲对增强可塑性的影响,结果表明较慢和较快的刺激率在增强可塑性方面效果较差。我们将这些结果与以前描述刺激参数对 VNS 依赖性可塑性和神经调制网络激活的影响的发现相结合,生成了 VNS 诱导突触激活的模型。