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劳拉西泮对人体运动皮质兴奋性的影响。

The effect of lorazepam on the motor cortical excitability in man.

作者信息

Ziemann U, Lönnecker S, Steinhoff B J, Paulus W

机构信息

Department of Clinical Neurophysiology, University of Göttingen, Germany.

出版信息

Exp Brain Res. 1996 Apr;109(1):127-35. doi: 10.1007/BF00228633.

DOI:10.1007/BF00228633
PMID:8740215
Abstract

The effect of the short-acting benzodiazepine lorazepam on motor cortex excitability was investigated in 11 healthy volunteers using the technique of focal transcranial magnetic stimulation. The threshold intensity for evoking an electromyographic response in the resting and active abductor digiti minimi muscle, the size of the motor evoked potential, the duration of the cortical and peripheral silent periods, the corticocortical inhibition and facilitation after paired magnetic stimuli, and the transcallosal inhibition were used as parameters to assess various aspects of motor system excitability. Baseline values were compared with data obtained 2, 5 and 24 h after a single oral dose of 2.5 mg lorazepam. Resting and active motor thresholds and the size of the motor evoked potential remained unchanged. The duration of the cortical silent period was prolonged with a maximum effect 5 h after drug intake, while the peripheral silent period did not show any lengthening at that time. The corticocortical inhibition showed a tendency toward more inhibition, while the corticocortical facilitation was almost completely suppressed. The transcallosal inhibition showed an inconsistent trend to less inhibition. In parallel to the pharmacokinetics of lorazepam, all effects peaked at 2 h and 5 h, and were (partially) reversible after 24 h. It is hypothesized that most of these findings are due to the reinforcement of GABA action by lorazepam at the level of the motor cortex. The lack of effect on motor threshold and on the size of the motor evoked potential may indicate that these parameters are physiologically distinct from corticocortical excitability and the cortical silent period. The relevance of the present data in clinical epileptology is discussed.

摘要

在11名健康志愿者中,采用局灶性经颅磁刺激技术研究了短效苯二氮䓬类药物劳拉西泮对运动皮质兴奋性的影响。以静息和主动状态下小指展肌诱发肌电图反应的阈值强度、运动诱发电位的大小、皮质和周围静息期的持续时间、配对磁刺激后的皮质皮质抑制和易化以及胼胝体抑制作为参数,评估运动系统兴奋性的各个方面。将基线值与单次口服2.5 mg劳拉西泮后2、5和24小时获得的数据进行比较。静息和主动运动阈值以及运动诱发电位的大小保持不变。皮质静息期的持续时间延长,服药后5小时达到最大效应,而此时周围静息期未出现延长。皮质皮质抑制呈现出更强抑制的趋势,而皮质皮质易化几乎完全被抑制。胼胝体抑制呈现出抑制减少的不一致趋势。与劳拉西泮的药代动力学平行,所有效应在2小时和5小时达到峰值,24小时后(部分)可逆。据推测,这些发现大多归因于劳拉西泮在运动皮质水平增强了γ-氨基丁酸(GABA)的作用。对运动阈值和运动诱发电位大小缺乏影响可能表明这些参数在生理上与皮质皮质兴奋性和皮质静息期不同。本文讨论了这些数据在临床癫痫学中的相关性。

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Effects of transcallosal volleys on pyramidal tract cell activity of cat.胼胝体传入冲动对猫锥体束细胞活动的影响。
J Neurophysiol. 1962 Mar;25:198-208. doi: 10.1152/jn.1962.25.2.198.
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Brain. 1995 Dec;118 ( Pt 6):1437-46. doi: 10.1093/brain/118.6.1437.
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The muscle silent period following transcranial magnetic cortical stimulation.经颅磁刺激皮层后的肌肉静息期。
重复配对脉冲经颅磁刺激联合β经颅交流电刺激作用于人类初级运动皮层后的效应所涉及的神经机制。
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Hallmarks of Brain Plasticity.脑可塑性的特征
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Contribution of Glutamatergic and GABAergic Mechanisms to the Plasticity-Modulating Effects of Dopamine in the Human Motor Cortex.谷氨酸能和γ-氨基丁酸能机制对多巴胺在人类运动皮层中可塑性调节作用的贡献。
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