Neurophysiological Characterization of Transpinal Evoked Potentials in Human Leg Muscles

被引:43
作者
Knikou, Maria [1 ]
机构
[1] CUNY, Grad Ctr, New York, NY USA
关键词
soleus H-reflex; low-frequency depression; electric stimulation; spine; multisegmental responses; thoracolumbar region; SPINAL-CORD STIMULATION; SOLEUS H-REFLEX; CERVICAL MAGNETIC STIMULATION; POST-ACTIVATION DEPRESSION; ELECTRICAL-STIMULATION; BRAIN-STIMULATION; VERTEBRAL COLUMN; EXCITABILITY; MOTONEURONS; MODULATION;
D O I
10.1002/bem.21808
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The objectives of this study were to characterize the neurophysiological properties of the compound muscle action potentials (CMAPs) evoked by transcutaneous electric stimulation of the spine (tsESS), and the effects of tsESS on the soleus H-reflex in seated and standing healthy human subjects. In seated semi-prone subjects with the trunk semi-flexed, two re-usable self-adhering electrodes (cathode), connected to act as one electrode, were placed bilaterally on the iliac crests. A re-usable pregelled electrode (anode) was placed on the thoracolumbar region at thoracic 10-lumbar 1 and held under constant pressure throughout the experiment. CMAPs were recorded bilaterally from ankle muscles with subjects seated semi-prone at 1.0, 0.3, 0.2, 0.125, and 0.1Hz following tsESS. The soleus H-reflex, evoked by posterior tibial nerve stimulation via conventional methods, was measured following tsESS at inter-stimulus intervals (ISIs) that ranged from -100 to 100ms with the subjects seated semi-prone and during standing. The tsESS-induced CMAPs were not decreased at low stimulation frequencies, and the soleus H-reflex excitability was profoundly decreased by tsESS at ISIs that ranged from -5 to 20ms with the subjects seated semi-prone and during standing. CMAPs induced by tsESS may be utilized to assess spinal-to-muscle conduction time while bypassing spinal motoneuron excitability and tsESS can be used as a modality to decrease spinal reflex hyper-excitability in neurological disorders. Bioelectromagnetics 34:630-640, 2013. (c) 2013 Wiley Periodicals, Inc.
引用
收藏
页码:630 / 640
页数:11
相关论文
共 43 条
[1]   Postvibration depression of the H-reflex as a result of a dual mechanism - An experimental study in humans [J].
Abbruzzese, M ;
Minatel, C ;
Reni, L ;
Favale, E .
JOURNAL OF CLINICAL NEUROPHYSIOLOGY, 2001, 18 (05) :460-470
[2]   Spinal direct current stimulation modulates the activity of gracile nucleus and primary somatosensory cortex in anaesthetized rats [J].
Aguilar, J. ;
Pulecchi, F. ;
Dilena, R. ;
Oliviero, A. ;
Priori, A. ;
Foffani, G. .
JOURNAL OF PHYSIOLOGY-LONDON, 2011, 589 (20) :4981-4996
[3]   Trans-spinal direct current stimulation modulates motor cortex-induced muscle contraction in mice [J].
Ahmed, Zaghloul .
JOURNAL OF APPLIED PHYSIOLOGY, 2011, 110 (05) :1414-1424
[4]  
BAYOUMI A, 1989, EXP BRAIN RES, V76, P223
[5]  
Brody DL, 2000, J NEUROSCI, V20, P2480
[6]   Tissue and electrode capacitance reduce neural activation volumes during deep brain stimulation [J].
Butson, CR ;
McIntyre, CC .
CLINICAL NEUROPHYSIOLOGY, 2005, 116 (10) :2490-2500
[7]   Paired-pulse depression of unitary quantal amplitude at single hippocampal synapses [J].
Chen, G ;
Harata, NC ;
Tsien, RW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (04) :1063-1068
[8]   PERCUTANEOUS MAGNETIC COIL STIMULATION OF HUMAN CERVICAL VERTEBRAL COLUMN - SITE OF STIMULATION AND CLINICAL-APPLICATION [J].
CHOKROVERTY, S ;
PICONE, MA ;
CHOKROVERTY, M .
ELECTROENCEPHALOGRAPHY AND CLINICAL NEUROPHYSIOLOGY, 1991, 81 (05) :359-365
[9]   A THEORETICAL-STUDY OF EPIDURAL ELECTRICAL-STIMULATION OF THE SPINAL-CORD .2. EFFECTS ON LONG MYELINATED FIBERS [J].
COBURN, B .
IEEE TRANSACTIONS ON BIOMEDICAL ENGINEERING, 1985, 32 (11) :978-986
[10]   Modulation of multisegmentalmonosynaptic responses in a variety of leg muscles during walking and running in humans [J].
Courtine, Gr Goire ;
Harkema, Susan J. ;
Dy, Christine J. ;
Gerasimenko, Yuri P. ;
Dyhre-Poulsen, Poul .
JOURNAL OF PHYSIOLOGY-LONDON, 2007, 582 (03) :1125-1139