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需要局部激活α2 肾上腺素能受体以实现迷走神经刺激诱导的运动皮质可塑性。

Local activation of α2 adrenergic receptors is required for vagus nerve stimulation induced motor cortical plasticity.

机构信息

School of Behavioral and Brain Sciences, University of Texas at Dallas, 800 W. Campbell Rd, Richardson, TX, 75080, USA.

出版信息

Sci Rep. 2021 Nov 4;11(1):21645. doi: 10.1038/s41598-021-00976-2.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b61/8568982/009470550e8d/41598_2021_976_Fig1_HTML.jpg

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