Spinal Direct Current Stimulation Modulates Short Intracortical Inhibition

被引:36
作者
Bocci, Tommaso [1 ,2 ]
Barloscio, Davide [1 ]
Vergari, Maurizio [3 ]
Di Rollo, Andrea [4 ]
Rossi, Simone [2 ]
Priori, Alberto [3 ]
Sartucci, Ferdinando [1 ,4 ,5 ]
机构
[1] Univ Pisa, Sch Med, Dept Clin & Expt Med, Neurol Unit, Via P Savi 40, I-56126 Pisa, Italy
[2] Azienda Osped Univ Senese, Dept Neurol & Neurosensorial Sci, Neurol & Clin Neurophysiol Sect, Brain Invest & Neuromodulat Lab, Siena, Italy
[3] Univ Milan, Fdn IRCCS Osped Maggiore Policlin, Dept Neurol Sci, Milan, Italy
[4] Azienda Osped Univ Pisana, Dept Clin & Expt Med, Cisanello Neurol Unit, Pisa, Italy
[5] CNR, Inst Neurosci, I-56100 Pisa, Italy
来源
NEUROMODULATION | 2015年 / 18卷 / 08期
关键词
Cortical silent period; motor system; short intracortical facilitation; short intracortical inhibition; transcutaneous spinal direct current stimulation; tsDCS; TRANSCRANIAL MAGNETIC STIMULATION; HUMAN MOTOR CORTEX; SOMATOSENSORY-EVOKED POTENTIALS; CORD STIMULATION; SILENT PERIOD; CORTICOCORTICAL INHIBITION; SUPRASPINAL MECHANISMS; LOCUS-COERULEUS; DC STIMULATION; RAPHE NEURONS;
D O I
10.1111/ner.12298
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Objective: Transcutaneous spinal direct current stimulation (tsDCS) is a new and safe technique for modulating spinal cord excitability. We assessed changes in intracortical excitability following tsDCS by evaluating changes in cortical silent period (cSP), paired-pulse short intracortical inhibition (SICI), and intracortical facilitation (ICF). Materials and Methods: Healthy subjects were studied before (T0) and at different intervals (T1 and T2) after anodal, cathodal, and sham tsDCS (20', 2.0 mA) applied over the thoracic spinal cord (T10-T12). We assessed changes in cSP, SICI (interstimulus interval, ISI = 3 ms) and ICF (ISI = 10 ms). Motor-evoked potentials (MEPs) were recorded from first digital interosseus (FDI) and tibialis anterior (TA) muscles. Results: Cathodal tsDCS increased MEP amplitudes at interstimulus interval of 3 ms, while anodal one elicited opposite effects (FDI: p = 0.0023; TA: p = 0.0004); conversely, tsDCS left MEP amplitudes unchanged at ISI of 10 ms (FDI: p = 0.39; TA: p = 0.45). No significant change in cSP duration was found from upper limb (p = 0.81) and lower limb (p = 0.33). Conclusion: tsDCS modulates inhibitory GABA(A) ergic drive, as assessed by SICI, without interfering with cSP and ICF. The possibility to interfere with cortical processing makes tsDCS a useful approach to modulate spinal drive through nonspinal mechanisms. tsDCS could also represent an early rehabilitation strategy in patients with acute brain lesions, when other noninvasive brain stimulation (NIBS) tools are not indicated due to safety concerns, as well as in the treatment of spinal diseases or pain syndromes.
引用
收藏
页码:686 / 693
页数:8
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