Primary Sensory and Motor Cortex Excitability Are Co-Modulated in Response to Peripheral Electrical Nerve Stimulation

被引:84
|
作者
Schabrun, Siobhan M. [1 ,2 ]
Ridding, Michael C. [3 ]
Galea, Mary P. [4 ]
Hodges, Paul W. [1 ,2 ]
Chipchase, Lucinda S. [1 ,2 ]
机构
[1] Univ Queensland, NHMRC Ctr Clin Res Excellence Spinal Pain Injury, Brisbane, Qld, Australia
[2] Univ Queensland, Sch Hlth & Rehabil Sci, Brisbane, Qld, Australia
[3] Univ Adelaide, Sch Paediat & Reprod Hlth, Robinson Inst, Adelaide, SA 5005, Australia
[4] Univ Melbourne, Rehabil Sci Res Ctr, Melbourne, Vic 3010, Australia
来源
PLOS ONE | 2012年 / 7卷 / 12期
基金
英国医学研究理事会;
关键词
TRANSCRANIAL MAGNETIC STIMULATION; SOMATOSENSORY EVOKED-POTENTIALS; SYSTEM AMPLIFICATION; FUNCTIONAL-ROLE; INPUT; PLASTICITY; HUMANS; MUSCLE; TENS; PAIN;
D O I
10.1371/journal.pone.0051298
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Peripheral electrical stimulation (PES) is a common clinical technique known to induce changes in corticomotor excitability; PES applied to induce a tetanic motor contraction increases, and PES at sub-motor threshold (sensory) intensities decreases, corticomotor excitability. Understanding of the mechanisms underlying these opposite changes in corticomotor excitability remains elusive. Modulation of primary sensory cortex (S1) excitability could underlie altered corticomotor excitability with PES. Here we examined whether changes in primary sensory (S1) and motor (M1) cortex excitability follow the same time-course when PES is applied using identical stimulus parameters. Corticomotor excitability was measured using transcranial magnetic stimulation (TMS) and sensory cortex excitability using somatosensory evoked potentials (SEPs) before and after 30 min of PES to right abductor pollicis brevis (APB). Two PES paradigms were tested in separate sessions; PES sufficient to induce a tetanic motor contraction (30-50 Hz; strong motor intensity) and PES at sub motor-threshold intensity (100 Hz). PES applied to induce strong activation of APB increased the size of the N-20-P-25 component, thought to reflect sensory processing at cortical level, and increased corticomotor excitability. PES at sensory intensity decreased the size of the P25-N33 component and reduced corticomotor excitability. A positive correlation was observed between the changes in amplitude of the cortical SEP components and corticomotor excitability following sensory and motor PES. Sensory PES also increased the sub-cortical P-14-N-20 SEP component. These findings provide evidence that PES results in co-modulation of S1 and M1 excitability, possibly due to cortico-cortical projections between S1 and M1. This mechanism may underpin changes in corticomotor excitability in response to afferent input generated by PES.
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页数:7
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