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Electrical Stimulation Able to Trigger Locomotor Spinal Circuits Also Induces Dorsal Horn Activity.

Bibliographic reference Dingu, Nejada ; Deumens, Ronald ; Taccola, Giuliano. Electrical Stimulation Able to Trigger Locomotor Spinal Circuits Also Induces Dorsal Horn Activity.. In: Neuromodulation, Vol. 19, no.1, p. 38-46 (2016)
Permanent URL http://hdl.handle.net/2078.1/172571
  1. Behrman Andrea L., Harkema Susan J., Physical Rehabilitation as an Agent for Recovery After Spinal Cord Injury, 10.1016/j.pmr.2007.02.002
  2. Grillner Sten, Biological Pattern Generation: The Cellular and Computational Logic of Networks in Motion, 10.1016/j.neuron.2006.11.008
  3. Goulding Martyn, Circuits controlling vertebrate locomotion: moving in a new direction, 10.1038/nrn2608
  4. Talpalar Adolfo E., Endo Toshiaki, Löw Peter, Borgius Lotta, Hägglund Martin, Dougherty Kimberly J., Ryge Jesper, Hnasko Thomas S., Kiehn Ole, Identification of Minimal Neuronal Networks Involved in Flexor-Extensor Alternation in the Mammalian Spinal Cord, 10.1016/j.neuron.2011.07.011
  5. DIMITRIJEVIC MILAN R., GERASIMENKO YURI, PINTER MICHAELA M., Evidence for a Spinal Central Pattern Generator in Humansa, 10.1111/j.1749-6632.1998.tb09062.x
  6. Hagglund M., Dougherty K. J., Borgius L., Itohara S., Iwasato T., Kiehn O., Optogenetic dissection reveals multiple rhythmogenic modules underlying locomotion, 10.1073/pnas.1304365110
  7. Kiehn Ole, LOCOMOTOR CIRCUITS IN THE MAMMALIAN SPINAL CORD, 10.1146/annurev.neuro.29.051605.112910
  8. Atsuta, J Neurophysiol, 64, 727 (1990)
  9. Taccola Giuliano, Mladinic Miranda, Nistri Andrea, Dynamics of early locomotor network dysfunction following a focal lesion in anin vitromodel of spinal injury, 10.1111/j.1460-9568.2009.07040.x
  10. Marchetti Cristina, Beato Marco, Nistri Andrea, Alternating rhythmic activity induced by dorsal root stimulation in the neonatal rat spinal cordin vitro, 10.1111/j.1469-7793.2001.0105m.x
  11. Kemler Marius A., Barendse Gerard A.M., van Kleef Maarten, de Vet Henrica C.W., Rijks Coen P.M., Furnée Carina A., van den Wildenberg Frans A.J.M., Spinal Cord Stimulation in Patients with Chronic Reflex Sympathetic Dystrophy, 10.1056/nejm200008313430904
  12. Smits Helwin, van Kleef Maarten, Holsheimer Jan, Joosten Elbert A. J., Experimental Spinal Cord Stimulation and Neuropathic Pain: Mechanism of Action, Technical Aspects, and Effectiveness : SCS in Neuropathic Pain, 10.1111/j.1533-2500.2012.00579.x
  13. Minassian K., Persy I., Rattay F., Pinter M.M., Kern H., Dimitrijevic M.R., Human lumbar cord circuitries can be activated by extrinsic tonic input to generate locomotor-like activity, 10.1016/j.humov.2007.01.005
  14. Matsuto Takayuki, Yanagisawa Mitsuhiko, Otsuka Masanori, Kanazawa Ichiro, Munekata Eisuke, The excitatory action of the newly-discovered mammalian tachykinins, neurokinin α and neurokinin β, on neurons of the isolated spinal cord of the newborn rat, 10.1016/0168-0102(84)90008-7
  15. Taccola Giuliano, Marchetti Cristina, Nistri Andrea, Effect of metabotropic glutamate receptor activity on rhythmic discharges of the neonatal rat spinal cord in vitro, 10.1007/s00221-003-1668-1
  16. Kjaerulff, J Neurosci, 16, 5777 (1996)
  17. Kudo Norio, Yamada Toshiya, locomotor activity in a spinal cord-indlimb muscles preparation of the newborn rat studied in vitro, 10.1016/0304-3940(87)90072-3
  18. Smith Jeffrey C., Feldman Jack L., In vitro brainstem-spinal cord preparations for study of motor systems for mammalian respiration and locomotion, 10.1016/0165-0270(87)90126-9
  19. Lev-Tov, J Neurophysiol, 83, 888 (2000)
  20. Eccles J. C., Schmidt R., Willis W. D., Pharmacological studies on presynaptic inhibition, 10.1113/jphysiol.1963.sp007205
  21. Randic, J Neurosci, 13, 5228 (1993)
  22. Ruscheweyh Ruth, Sandkühler Jürgen, Epileptiform activity in rat spinal dorsal horn in vitro has common features with neuropathic pain : , 10.1016/s0304-3959(03)00248-3
  23. Deumens R., Mazzone G.L., Taccola G., Early spread of hyperexcitability to caudal dorsal horn networks after a chemically-induced lesion of the rat spinal cord in vitro, 10.1016/j.neuroscience.2012.10.036
  24. Visockis V., King A.E., M-channels modulate network excitatory activity induced by 4-aminopyridine in immature rat substantia gelatinosa in vitro, 10.1016/j.brainres.2013.03.045
  25. Wu Sheng-Xi, Wang Wen, Li Hui, Wang Ya-Yun, Feng Yu-Peng, Li Yun-Qing, The synaptic connectivity that underlies the noxious transmission and modulation within the superficial dorsal horn of the spinal cord, 10.1016/j.pneurobio.2010.01.005
  26. Parker John L., Karantonis Dean M., Single Peter S., Obradovic Milan, Cousins Michael J., Compound action potentials recorded in the human spinal cord during neurostimulation for pain relief : , 10.1016/j.pain.2011.11.023
  27. Willis Jr. W. D., Dorsal root potentials and dorsal root reflexes: a double-edged sword, 10.1007/s002210050637
  28. Gossard, J Neurophysiol, 62, 1177 (1989)
  29. Gossard Jean-Pierre, Cabelguen Jean-Marie, Rossignol Serge, Phase-dependent modulation of primary afferent depolarization in single cutaneous primary afferents evoked by peripheral stimulation during fictive locomotion in the cat, 10.1016/0006-8993(90)90334-8
  30. Duenas, Exp Brain Res, 70, 15 (1988)
  31. Duenas, J Neurophysiol, 63, 1467 (1990)
  32. Gossard, J Neurophysiol, 65, 914 (1991)
  33. Gossard, J Neurophysiol, 76, 4104 (1996)
  34. Menard, J Neurosci, 19, 391 (1999)
  35. Gossard Jean-Pierre, Rossignol Serge, Phase-dependent modulation of dorsal root potentials evoked by peripheral nerve stimulation during fictive locomotion in the cat, 10.1016/0006-8993(90)90333-7
  36. El Manira A., Tegner J., Grillner S., Locomotor-Related Presynaptic Modulation of Primary Afferents in the Lamprey, 10.1111/j.1460-9568.1997.tb01418.x
  37. Hochman Shawn, Hayes Heather Brant, Speigel Iris, Chang Young-Hui, Force-sensitive afferents recruited during stance encode sensory depression in the contralateral swinging limb during locomotion : Stance force control of afferents in swinging limb, 10.1111/nyas.12055
  38. Hayes H. B., Chang Y.-H., Hochman S., Stance-phase force on the opposite limb dictates swing-phase afferent presynaptic inhibition during locomotion, 10.1152/jn.01134.2011
  39. Taccola G., Nistri A., Characteristics of the electrical oscillations evoked by 4-aminopyridine on dorsal root fibers and their relation to fictive locomotor patterns in the rat spinal cord in vitro, 10.1016/j.neuroscience.2005.02.012
  40. Koga Kohei, Furue Hidemasa, Rashid Md Harunor, Takaki Atsushi, Katafuchi Toshihiko, Yoshimura Megumu, Selective Activation of Primary Afferent Fibers Evaluated by Sine-Wave Electrical Stimulation, 10.1186/1744-8069-1-13
  41. Marchetti Cristina, Beato Marco, Nistri Andrea, Evidence for increased extracellular K+ as an important mechanism for dorsal root induced alternating rhythmic activity in the neonatal rat spinal cord in vitro, 10.1016/s0304-3940(01)01777-3
  42. Taccola G., Olivieri D., D’Angelo G., Blackburn P., Secchia L., Ballanyi K., A1 adenosine receptor modulation of chemically and electrically evoked lumbar locomotor network activity in isolated newborn rat spinal cords, 10.1016/j.neuroscience.2012.07.030
  43. Dose F., Taccola G., Coapplication of noisy patterned electrical stimuli and NMDA plus serotonin facilitates fictive locomotion in the rat spinal cord, 10.1152/jn.00554.2012
  44. Schück Alex, Labruyère Rob, Vallery Heike, Riener Robert, Duschau-Wicke Alexander, Feasibility and effects of patient-cooperative robot-aided gait training applied in a 4-week pilot trial, 10.1186/1743-0003-9-31
  45. Gossard Jean-Pierre, Bouyer Laurent, Rossignol Serge, The effects of antidromic discharges on orthodromic firing of primary afferents in the cat, 10.1016/s0006-8993(99)01236-6
  46. Vinay, J Physiol, 93, 359 (1999)
  47. Juvin Laurent, Simmers John, Morin Didier, Locomotor rhythmogenesis in the isolated rat spinal cord: a phase-coupled set of symmetrical flexion-extension oscillators : Motor burst timing during quadrupedal locomotion, 10.1113/jphysiol.2007.133413
  48. Calancie Blair, Broton James G., John Klose K., Traad Monique, Difini John, Ram Ayyar D., Evidence that alterations in presynaptic inhibition contribute to segmental hypo- and hyperexcitability after spinal cord injury in man, 10.1016/0168-5597(93)90131-8
  49. Molnar Gabriela, Barolat Giancarlo, Principles of Cord Activation During Spinal Cord Stimulation : Principles of Spinal Cord Stimulation, 10.1111/ner.12171
  50. Dose F, Deumens R, Forget P, Taccola G, Staggered multi-site low-frequency electrostimulation effectively induces locomotor patterns in the isolated rat spinal cord, 10.1038/sc.2015.106