School of Behavioral and Brain Sciences, University of Texas at Dallas, 800 W. Campbell Rd, Richardson, TX, 75080, USA.
Sci Rep. 2021 Nov 4;11(1):21645. doi: 10.1038/s41598-021-00976-2.
Vagus nerve stimulation (VNS) paired with rehabilitation training is emerging as a potential treatment for improving recovery of motor function following stroke. In rats, VNS paired with skilled forelimb training results in significant reorganization of the somatotopic cortical motor map; however, the mechanisms underlying this form of VNS-dependent plasticity remain unclear. Recent studies have shown that VNS-driven cortical plasticity is dependent on noradrenergic innervation of the neocortex. In the central nervous system, noradrenergic α2 receptors (α2-ARs) are widely expressed in the motor cortex and have been critically implicated in synaptic communication and plasticity. In current study, we examined whether activation of cortical α2-ARs is necessary for VNS-driven motor cortical reorganization to occur. Consistent with previous studies, we found that VNS paired with motor training enlarges the map representation of task-relevant musculature in the motor cortex. Infusion of α2-AR antagonists into M1 blocked VNS-driven motor map reorganization from occurring. Our results suggest that local α2-AR activation is required for VNS-induced cortical reorganization to occur, providing insight into the mechanisms that may underlie the neuroplastic effects of VNS therapy.
迷走神经刺激(VNS)与康复训练相结合,正在成为改善中风后运动功能恢复的一种潜在治疗方法。在大鼠中,VNS 与熟练的前肢训练相结合,导致躯体感觉皮层运动图的显著重组;然而,这种形式的 VNS 依赖可塑性的机制尚不清楚。最近的研究表明,VNS 驱动的皮质可塑性依赖于新皮质的去甲肾上腺素能神经支配。在中枢神经系统中,去甲肾上腺素能α2 受体(α2-AR)广泛表达于运动皮质,并被认为与突触通讯和可塑性密切相关。在目前的研究中,我们研究了皮质α2-AR 的激活是否是 VNS 驱动的运动皮质重组发生所必需的。与先前的研究一致,我们发现,VNS 与运动训练相结合,扩大了运动皮质中与任务相关肌肉的图谱表示。将 α2-AR 拮抗剂注入 M1 可阻止 VNS 驱动的运动图谱重组的发生。我们的结果表明,局部α2-AR 的激活是 VNS 诱导的皮质重组发生所必需的,这为 VNS 治疗的神经可塑性效应的潜在机制提供了深入了解。