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Publication Detail
The facilitatory effects of intermittent theta burst stimulation on corticospinal excitability are enhanced by nicotine
  • Publication Type:
    Journal article
  • Publication Sub Type:
    Article
  • Authors:
    Swayne OBC, Teo JTH, Greenwood RJ, Rothwell JC
  • Publication date:
    08/2009
  • Pagination:
    1610, 1615
  • Journal:
    Clinical Neurophysiology
  • Volume:
    120
  • Issue:
    8
  • Print ISSN:
    1388-2457
  • Keywords:
    acetylcholine, Adult, agonists, AMPLITUDE, Analysis of Variance, Animal, ARM, article, Biophysics, clinical trial, CONTROLLED TRIAL, CORTEX, CORTICAL EXCITABILITY, corticospinal, Cross-Over Studies, DISORDERS, DOUBLE BLIND, Double-Blind Method, drug effects, effect, Electromyography, Evoked Potentials, Motor, EXCITABILITY, FACILITATION, Female, HEALTHY, HEALTHY SUBJECTS, Human, HUMANS, INDUCTION, LONG, LONG TERM, LONG TERM POTENTIATION, Male, MEP, MEPs, Methods, MODEL, MODELS, MODULATION, MOTOR, MOTOR CORTEX, motor evoked potential, MOTOR EVOKED POTENTIALS, Movement, MOVEMENT DISORDER, MOVEMENT DISORDERS, Neurology, NICOTINE, Nicotinic Agonists, pharmacology, PLASTICITY, POTENTIALS, POTENTIATION, PRIMARY, PRIMARY MOTOR CORTEX, pyramidal tracts, RECEPTORS, STIMULATION, Theta Rhythm, Time Factors, transcranial magnetic stimulation
Abstract
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 60min after subjects took either 4mg nicotine or placebo lozenges, and motor-evoked potentials (MEPs) were then recorded for 40min after the end of stimulation. RESULTS: In the placebo arm, iTBS produced an increase in the amplitudes of MEPs which lasted for 5min. In the nicotine arm, iTBS produced a more pronounced facilitation of MEPs that was still present at 40min. 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
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