全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Trains of Epidural DC Stimulation of the Cerebellum Tune Corticomotor Excitability

DOI: 10.1155/2013/613197

Full-Text   Cite this paper   Add to My Lib

Abstract:

We assessed the effects of anodal/cathodal direct current stimulation (DCS) applied epidurally over the cerebellum. We studied the excitability of both the motor cortex and the anterior horn of the spinal cord in adult rats under continuous anesthesia. We also investigated the effects on the spatial representation of a couple of agonist/antagonist muscles on primary motor cortex. Moreover, we evaluated the effects on the afferent inhibition in a paradigm of conditioned corticomotor responses. Anodal DCS of the cerebellum (1) decreased the excitability of the motor cortex, (2) reduced the excitability of waves, as shown by the decrease of both mean /mean ratios and persistence of waves, (3) exerted a “smoothing effect” on corticomotor maps, reshaping the representation of muscles on the motor cortex, and (4) enhanced the afferent inhibition of conditioned motor evoked responses. Cathodal DCS of the cerebellum exerted partially reverse effects. DCS of the cerebellum modulates the excitability of both motor cortex and spinal cord at the level of the anterior horn. This is the first demonstration that cerebellar DCS tunes the shape of corticomotor maps. Our findings provide a novel mechanism by which DCS of the cerebellum exerts a remote neuromodulatory effect upon motor cortex. 1. Introduction The dynamic modulation of the excitability of the motor cortex is critical for motor control. It depends on several elemental parameters: the excitability of single cells, the synaptic strength, and the balance between excitatory cells and inhibitory cells [1, 2]. The cerebellum is one of the subcortical structures modulating the excitability of the motor cortex and the spinal cord [3]. It is presumed that defects in the tuning of the excitability of the corticomotor responses contribute to the sensorimotor learning deficits in cerebellar patients [4]. Since we currently lack efficient therapies in numerous forms of cerebellar disorders encountered during daily practice, there is a need to identify novel strategies that might be used to antagonize cerebellar motor deficits. The mechanisms of these deficits depend on the type of cerebellar damage. Indeed, cerebellar cortex inhibits strongly cerebellar nuclei, which themselves stimulate contralateral motor cortex and ipsilateral anterior horn of the spinal cord. Therefore, cerebellar cortical lesions induce a disinhibition of cerebellar nuclei, which results in an excitatory overdrive along the dentatothalamocortical pathway [5]. When the lesion is extensive and includes cerebellar nuclei, such as in hemicerebellar

References

[1]  A. R. Luft, A. Kaelin-Lang, T. K. Hauser et al., “Modulation of rodent cortical motor excitability by somatosensory input,” Experimental Brain Research, vol. 142, no. 4, pp. 562–569, 2002.
[2]  M. Manto, N. Oulad Ben Taib, and A. R. Luft, “Modulation of excitability as an early change leading to structural adaptation in the motor cortex,” The Journal of Neuroscience Research, vol. 83, no. 2, pp. 177–180, 2006.
[3]  N. Oulad Ben Taib, M. A. Laute, M. Pandolfo, and M. U. Manto, “Interaction between repetitive stimulation of the sciatic nerve and functional ablation of cerebellar nucleus interpositus in the rat,” Cerebellum, vol. 3, no. 1, pp. 21–26, 2004.
[4]  N. Oulad Ben Taib and M. Manto, “Trains of transcranial direct current stimulation antagonize motor cortex hypoexcitability induced by acute hemicerebellectomy: laboratory investigation,” Journal of Neurosurgery, vol. 111, no. 4, pp. 796–806, 2009.
[5]  M. Manto, D. Gruol, J. D. Schmahmann, N. Koibuchi, and F. Rossi, Handbook of the Cerebellum and Cerebellar Disorders, Springer, New York, NY, USA, 2013.
[6]  J. M. Galea, A. Vazquez, N. Pasricha, J. J. O. de Xivry, and P. Celnik, “Dissociating the roles of the cerebellum and motor cortex during adaptive learning: the motor cortex retains what the cerebellum learns,” Cerebral Cortex, vol. 21, no. 8, pp. 1761–1770, 2011.
[7]  G. Jayaram, B. Tang, R. Pallegadda, E. V. Vasudevan, P. Celnik, and A. Bastian, “Modulating locomotor adaptation with cerebellar stimulation,” Journal of Neurophysiology, vol. 107, pp. 2950–2957, 2012.
[8]  J. M. Galea, G. Jayaram, L. Ajagbe, and P. Celnik, “Modulation of cerebellar excitability by polarity-specific noninvasive direct current stimulation,” The Journal of Neuroscience, vol. 29, no. 28, pp. 9115–9122, 2009.
[9]  J. Márquez-Ruiz, R. Leal-Campanario, R. Sánchez-Campusano et al., “Transcranial direct-current stimulation modulates synaptic mechanisms involved in associative learning in behaving rabbits,” Proceedings of the National Academy of Sciences of the United States of America, vol. 109, pp. 6710–6715, 2012.
[10]  M. A. Nitsche, A. Schauenburg, N. Lang et al., “Facilitation of implicit motor learning by weak transcranial direct current stimulation of the primary motor cortex in the human,” Journal of Cognitive Neuroscience, vol. 15, no. 4, pp. 619–626, 2003.
[11]  M. A. Nitsche and W. Paulus, “Sustained excitability elevations induced by transcranial DC motor cortex stimulation in humans,” Neurology, vol. 57, no. 10, pp. 1899–1901, 2001.
[12]  P. S. Boggio, F. Bermpohl, A. O. Vergara et al., “Go-no-go task performance improvement after anodal transcranial DC stimulation of the left dorsolateral prefrontal cortex in major depression,” Journal of Affective Disorders, vol. 101, no. 1–3, pp. 91–98, 2007.
[13]  N. Oulad Ben Taib, M. Manto, M. A. Laute, and J. Brotchi, “The cerebellum modulates rodent cortical motor output after repetitive somatosensory stimulation,” Neurosurgery, vol. 56, no. 4, pp. 811–820, 2005.
[14]  N. Oulad Ben Taib and M. Manto, “Effects of trains of high-frequency stimulation of the premotor/supplementary motor area on conditioned corticomotor responses in hemicerebellectomized rats,” Experimental Neurology, vol. 212, no. 1, pp. 157–165, 2008.
[15]  X. Y. Chen, J. S. Carp, L. Chen, and J. R. Wolpaw, “Sensorimotor cortex ablation prevents H-reflex up-conditioning and causes a paradoxical response to down-conditioning in rats,” Journal of Neurophysiology, vol. 96, no. 1, pp. 119–127, 2006.
[16]  K. Molina-Luna, M. M. Buitrago, B. Hertler et al., “Cortical stimulation mapping using epidurally implanted thin-film microelectrode arrays,” Journal of Neuroscience Methods, vol. 161, no. 1, pp. 118–125, 2007.
[17]  N. Oulad Ben Taib, M. Mario, P. Massimo, and B. Jacques, “Hemicerebellectomy blocks the enhancement of cortical motor output associated with repetitive somatosensory stimulation in the rat,” Journal of Physiology, vol. 567, no. 1, pp. 293–300, 2005.
[18]  M. K. Floeter, “Spinal reflexes,” in Handbook of Clinical Neurophysiology, M. Hallett, Ed., pp. 231–246, Elsevier, Amsterdam, The Netherlands, 2003.
[19]  M. Gozariu, V. Roth, F. Keime, D. Le Bars, and J. C. Willer, “An electrophysiological investigation into the monosynaptic H-reflex in the rat,” Brain Research, vol. 782, no. 1-2, pp. 343–347, 1998.
[20]  G. Paxinos and C. Watson, The Rat Brain in Stereotaxic Coordinates, Academic Press, San Diego, Calif, USA, 1986.
[21]  F. Fregni, D. Liebetanz, K. K. Monte-Silva et al., “Effects of transcranial direct current stimulation coupled with repetitive electrical stimulation on cortical spreading depression,” Experimental Neurology, vol. 204, no. 1, pp. 462–466, 2007.
[22]  D. Liebetanz, F. Klinker, D. Hering et al., “Anticonvulsant effects of transcranial direct-current stimulation (tDCS) in the rat cortical ramp model of focal epilepsy,” Epilepsia, vol. 47, no. 7, pp. 1216–1224, 2006.
[23]  M. A. Nitsche, A. Seeber, K. Frommann et al., “Modulating parameters of excitability during and after transcranial direct current stimulation of the human motor cortex,” Journal of Physiology, vol. 568, no. 1, pp. 291–303, 2005.
[24]  M. P. Lomarev, D. Y. Kim, S. P. Richardson, B. Voller, and M. Hallett, “Safety study of high-frequency transcranial magnetic stimulation in patients with chronic stroke,” Clinical Neurophysiology, vol. 118, no. 9, pp. 2072–2075, 2007.
[25]  J. N. Sanes and J. P. Donoghue, “Plasticity and primary motor cortex,” Annual Review of Neuroscience, vol. 23, pp. 393–415, 2000.
[26]  D. A. Nowak, H. Topka, D. Timmann, H. Boecker, and J. Hermsd?rfer, “The role of the cerebellum for predictive control of grasping,” Cerebellum, vol. 6, no. 1, pp. 7–17, 2007.
[27]  N. K. Iwata and Y. Ugawa, “The effects of cerebellar stimulation on the motor cortical excitability in neurological disorders: a review,” Cerebellum, vol. 4, no. 4, pp. 218–223, 2005.
[28]  Y. Ugawa, Y. Uesaka, Y. Terao, R. Hanajima, and I. Kanazawa, “Magnetic stimulation over the cerebellum humans,” Annals of Neurology, vol. 37, no. 6, pp. 703–713, 1995.
[29]  M. Oliveri, S. Torriero, G. Koch, S. Salerno, L. Petrosini, and C. Caltagirone, “The role of transcranial magnetic stimulation in the study of cerebellar cognitive function,” Cerebellum, vol. 6, no. 1, pp. 95–101, 2007.
[30]  V. Di Lazzaro, M. Molinari, D. Restuccia et al., “Cerebro-cerebellar interactions in man: neurophysiological studies in patients with focal cerebellar lesions,” Electroencephalography and Clinical Neurophysiology, vol. 93, no. 1, pp. 27–34, 1994.
[31]  B. Fierro, G. Giglia, A. Palermo, C. Pecoraro, S. Scalia, and F. Brighina, “Modulatory effects of 1 Hz rTMS over the cerebellum on motor cortex excitability,” Experimental Brain Research, vol. 176, no. 3, pp. 440–447, 2007.
[32]  H. Bantli and J. R. Bloedel, “The action of the dentate nucleus on the excitability of spinal motoneurons via pathways which do not involve the primary sensorimotor cortex,” Brain Research, vol. 88, no. 1, pp. 86–90, 1975.
[33]  I. S. Cooper, “Twenty-five years of experience with physiological neurosurgery,” Neurosurgery, vol. 9, no. 2, pp. 190–200, 1981.
[34]  L. Marshall, M. M?lle, M. Hallschmid, and J. Born, “Transcranial direct current stimulation during sleep improves declarative memory,” Journal of Neuroscience, vol. 24, no. 44, pp. 9985–9992, 2004.
[35]  A. Quartarone, N. Lang, V. Rizzo et al., “Motor cortex abnormalities in amyotrophic lateral sclerosis with transcranial direct-current stimulation,” Muscle and Nerve, vol. 35, no. 5, pp. 620–624, 2007.
[36]  D. J. L. G. Schutter and J. van Honk, “An electrophysiological link between the cerebellum, cognition and emotion: frontal theta EEG activity to single-pulse cerebellar TMS,” NeuroImage, vol. 33, no. 4, pp. 1227–1231, 2006.
[37]  A. Boehringer, K. Macher, J. Dukart, A. Villringer, and B. Pleger, “Cerebellar transcranial direct current stimulation modulates verbal working memory,” Brain Stimulation. In press.
[38]  H. J. Block and P. Celnik, “Can cerebellar transcranial direct current stimulation become a valuable neurorehabilitation intervention?” Expert Review of Neurotherapeutics, vol. 12, pp. 1275–1277, 2012.
[39]  C. A. Terzuolo and T. H. Bullock, “Measurement of imposed voltage gradient adequate to modulate neuronal firing,” Proceedings of the National Academy of Sciences of the United States of America, vol. 42, pp. 687–694, 1956.
[40]  D. P. Purpura and J. G. McMurtry, “Intracellular activities and evoked potential changes during polarization of motor cortex,” Journal of Neurophysiology, vol. 28, pp. 166–185, 1965.

Full-Text

comments powered by Disqus

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133

WeChat 1538708413