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配对关联刺激诱导人类腕屈肌 Ia 终端突触前抑制的变化。

Paired associative stimulation induces change in presynaptic inhibition of Ia terminals in wrist flexors in humans.

机构信息

Human Motor Control Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.

出版信息

J Neurophysiol. 2010 Aug;104(2):755-64. doi: 10.1152/jn.00761.2009. Epub 2010 Jun 10.

Abstract

Enhancements in the strength of corticospinal projections to muscles are induced in conscious humans by paired associative stimulation (PAS) to the motor cortex. Although most of the previous studies support the hypothesis that the increase of the amplitude of motor evoked potentials (MEPs) by PAS involves long-term potentiation (LTP)-like mechanism in cortical synapses, changes in spinal excitability after PAS have been reported, suggestive of parallel modifications in both cortical and spinal excitability. In a first series of experiments (experiment 1), we confirmed that both flexor carpi radialis (FCR) MEPs and FCR H reflex recruitment curves are enhanced by PAS. To elucidate the mechanism responsible for this change in the H reflex amplitude, we tested, using the same subjects, the hypothesis that enhanced H reflexes are caused by a down-regulation of the efficacy of mechanisms controlling Ia afferent discharge, including presynaptic Ia inhibition and postactivation depression. To address this question, amounts of both presynaptic Ia inhibition of FCR Ia terminals (D1 and D2 inhibitions methods; experiment 2) and postactivation depression (experiment 3) were determined before and after PAS. Results showed that PAS induces a significant decrease of presynaptic Ia inhibition of FCR terminals, which was concomitant with the facilitation of the H reflex. Postactivation depression was unaffected by PAS. It is argued that enhancement of segmental excitation by PAS relies on a selective effect of PAS on the interneurons controlling presynaptic inhibition of Ia terminals.

摘要

经颅磁刺激对大脑皮层的刺激可增强皮质脊髓投射到肌肉的强度。虽然大多数先前的研究支持这样的假设,即经颅磁刺激引起运动诱发电位(MEP)幅度的增加涉及皮质突触中的长时程增强(LTP)样机制,但经颅磁刺激后脊髓兴奋性的变化已经被报道,提示皮质和脊髓兴奋性的平行变化。在一系列实验中(实验 1),我们证实经颅磁刺激既能增强桡侧腕屈肌(FCR)MEP,又能增强 FCR H 反射募集曲线。为了阐明 H 反射幅度变化的机制,我们使用相同的受试者测试了以下假设:增强的 H 反射是由控制 Ia 传入放电的机制(包括突触前 Ia 抑制和后激活抑制)效能下调引起的。为了解决这个问题,我们使用 D1 和 D2 抑制法(实验 2)和后激活抑制法(实验 3)分别测定 FCR Ia 末梢的突触前 Ia 抑制(D1 和 D2 抑制法;实验 2)和后激活抑制(实验 3)的数量。结果表明,经颅磁刺激可显著降低 FCR 末梢的突触前 Ia 抑制,这与 H 反射的易化同时发生。后激活抑制不受经颅磁刺激的影响。经颅磁刺激增强节段兴奋性的机制在于经颅磁刺激对控制 Ia 末梢突触前抑制的中间神经元的选择性作用。

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