The facilitatory effects of intermittent theta burst stimulation on corticospinal excitability are enhanced by nicotine

被引:21
|
作者
Swayne, Orlando B. C. [1 ]
Teo, James T. H. [1 ]
Greenwood, Richard J. [2 ]
Rothwell, John C. [1 ]
机构
[1] UCL, Inst Neurol, Sobell Dept Motor Neurosci & Movement Disorders, London WC1N 3BG, England
[2] Natl Hosp Neurol & Neurosurg, Acute Stroke & Brain Injury Unit, London WC1N 3BG, England
基金
英国医学研究理事会;
关键词
Plasticity; Transcranial magnetic stimulation; Long term potentiation; Neuromodulation; Nicotine; Theta burst stimulation; LONG-TERM POTENTIATION; HUMAN MOTOR CORTEX; TRANSCRANIAL MAGNETIC STIMULATION; MOUSE DENTATE GYRUS; ACETYLCHOLINE-RECEPTORS; IN-VIVO; CORTICAL EXCITABILITY; ACTIVATION; PLASTICITY; NEUROPLASTICITY;
D O I
10.1016/j.clinph.2009.06.013
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: Intermittent theta burst Stimulation (iTBS) is increasingly widely used as a means of facilitating corticospinal excitability in the human primary motor cortex. This form of facilitatory plasticity within the stimulated cortex may occur by induction of long term potentiation (LTP). In animal models, agonists of nicotinic acetylcholine receptors have been shown to modulate or induce LTP; we thus sought to test whether nicotine may modulate the effects of iTBS on corticospinal excitability in humans. Methods: A double-blind placebo-controlled cross-over design study was conducted with 10 healthy subjects. iTBS was delivered 60 min after subjects took either 4 mg nicotine or placebo lozenges, and motor-evoked potentials (MEPs) were then recorded for 40 min after the end of stimulation. Results: In the placebo arm, iTBS produced an increase in the amplitudes of MEPs which lasted for 5 min. In the nicotine arm, iTBS produced a more pronounced facilitation of MEPs that was still present at 40 min. In a control experiment, nicotine alone had no effect on MEP amplitudes when given in the absence of iTBS. Conclusions: These data indicate that the effects of iTBS can be enhanced and prolonged by nicotine. Significance: These results are consistent with animal models demonstrating nicotinic modulation of facilitatory plasticity, and will be of interest to investigators seeking to enhance artificially induced changes in cortical excitability. (C) 2009 International Federation of Clinical Neurophysiology. Published by Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:1610 / 1615
页数:6
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