Literature DB >> 15124000

Stepping-like movements in humans with complete spinal cord injury induced by epidural stimulation of the lumbar cord: electromyographic study of compound muscle action potentials.

K Minassian1, B Jilge, F Rattay, M M Pinter, H Binder, F Gerstenbrand, M R Dimitrijevic.   

Abstract

STUDY
DESIGN: It has been previously demonstrated that sustained nonpatterned electric stimulation of the posterior lumbar spinal cord from the epidural space can induce stepping-like movements in subjects with chronic, complete spinal cord injury. In the present paper, we explore physiologically related components of electromyographic (EMG) recordings during the induced stepping-like activity.
OBJECTIVES: To examine mechanisms underlying the stepping-like movements activated by electrical epidural stimulation of posterior lumbar cord structures.
MATERIALS AND METHODS: The study is based on the assessment of epidural stimulation to control spasticity by simultaneous recordings of the electromyographic activity of quadriceps, hamstrings, tibialis anterior, and triceps surae. We examined induced muscle responses to stimulation frequencies of 2.2-50 Hz in 10 subjects classified as having a motor complete spinal cord injury (ASIA A and B). We evaluated stimulus-triggered time windows 50 ms in length from the original EMG traces. Stimulus-evoked compound muscle action potentials (CMAPs) were analyzed with reference to latency, amplitude, and shape.
RESULTS: Epidural stimulation of the posterior lumbosacral cord recruited lower limb muscles in a segmental-selective way, which was characteristic for posterior root stimulation. A 2.2 Hz stimulation elicited stimulus-coupled CMAPs of short latency which were approximately half that of phasic stretch reflex latencies for the respective muscle groups. EMG amplitudes were stimulus-strength dependent. Stimulation at 5-15 and 25-50 Hz elicited sustained tonic and rhythmic activity, respectively, and initiated lower limb extension or stepping-like movements representing different levels of muscle synergies. All EMG responses, even during burst-style phases were composed of separate stimulus-triggered CMAPs with characteristic amplitude modulations. During burst-style phases, a significant increase of CMAP latencies by about 10 ms was observed.
CONCLUSION: The muscle activity evoked by epidural lumbar cord stimulation as described in the present study was initiated within the posterior roots. These posterior roots muscle reflex responses (PRMRRs) to 2.2 Hz stimulation were routed through monosynaptic pathways. Sustained stimulation at 5-50 Hz engaged central spinal PRMRR components. We propose that repeated volleys delivered to the lumbar cord via the posterior roots can effectively modify the central state of spinal circuits by temporarily combining them into functional units generating integrated motor behavior of sustained extension and rhythmic flexion/extension movements. This study opens the possibility for developing neuroprostheses for activation of inherent spinal networks involved in generating functional synergistic movements using a single electrode implanted in a localized and stable region.

Entities:  

Mesh:

Year:  2004        PMID: 15124000     DOI: 10.1038/sj.sc.3101615

Source DB:  PubMed          Journal:  Spinal Cord        ISSN: 1362-4393            Impact factor:   2.772


  77 in total

1.  Unique Spatiotemporal Neuromodulation of the Lumbosacral Circuitry Shapes Locomotor Success after Spinal Cord Injury.

Authors:  Prithvi K Shah; Shakthi Sureddi; Monzurul Alam; Hui Zhong; Roland R Roy; V Reggie Edgerton; Yury Gerasimenko
Journal:  J Neurotrauma       Date:  2016-04-20       Impact factor: 5.269

2.  Intraspinal microstimulation preferentially recruits fatigue-resistant muscle fibres and generates gradual force in rat.

Authors:  J A Bamford; C T Putman; V K Mushahwar
Journal:  J Physiol       Date:  2005-10-20       Impact factor: 5.182

3.  Epidural stimulation induced modulation of spinal locomotor networks in adult spinal rats.

Authors:  Igor Lavrov; Christine J Dy; Andy J Fong; Yury Gerasimenko; Grégoire Courtine; Hui Zhong; Roland R Roy; V Reggie Edgerton
Journal:  J Neurosci       Date:  2008-06-04       Impact factor: 6.167

4.  Upper-limb muscle responses to epidural, subdural and intraspinal stimulation of the cervical spinal cord.

Authors:  Abigail N Sharpe; Andrew Jackson
Journal:  J Neural Eng       Date:  2014-02       Impact factor: 5.379

5.  Electrical neuromodulation of the cervical spinal cord facilitates forelimb skilled function recovery in spinal cord injured rats.

Authors:  Monzurul Alam; Guillermo Garcia-Alias; Benita Jin; Jonathan Keyes; Hui Zhong; Roland R Roy; Yury Gerasimenko; Daniel C Lu; V Reggie Edgerton
Journal:  Exp Neurol       Date:  2017-02-10       Impact factor: 5.330

6.  Phase-dependent modulation of percutaneously elicited multisegmental muscle responses after spinal cord injury.

Authors:  Christine J Dy; Yury P Gerasimenko; V Reggie Edgerton; Poul Dyhre-Poulsen; Grégoire Courtine; Susan J Harkema
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Review 7.  Activity-dependent plasticity in spinal cord injury.

Authors:  James V Lynskey; Adam Belanger; Ranu Jung
Journal:  J Rehabil Res Dev       Date:  2008

8.  Hindlimb movement in the cat induced by amplitude-modulated stimulation using extra-spinal electrodes.

Authors:  Changfeng Tai; Jicheng Wang; Bing Shen; Xianchun Wang; James R Roppolo; William C de Groat
Journal:  J Neural Eng       Date:  2008-03-26       Impact factor: 5.379

9.  Effect of epidural stimulation of the lumbosacral spinal cord on voluntary movement, standing, and assisted stepping after motor complete paraplegia: a case study.

Authors:  Susan Harkema; Yury Gerasimenko; Jonathan Hodes; Joel Burdick; Claudia Angeli; Yangsheng Chen; Christie Ferreira; Andrea Willhite; Enrico Rejc; Robert G Grossman; V Reggie Edgerton
Journal:  Lancet       Date:  2011-05-19       Impact factor: 79.321

10.  Periodic modulation of repetitively elicited monosynaptic reflexes of the human lumbosacral spinal cord.

Authors:  Ursula S Hofstoetter; Simon M Danner; Brigitta Freundl; Heinrich Binder; Winfried Mayr; Frank Rattay; Karen Minassian
Journal:  J Neurophysiol       Date:  2015-04-22       Impact factor: 2.714

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