|
|
||||||||
Journal of Neurophysiology, Vol 72, Issue 1 431-442, Copyright © 1994 by APS
ARTICLES |
J. S. Carp and J. R. Wolpaw
Wadsworth Center for Laboratories and Research, New York State Department of Health, Albany.
1. Monkeys can gradually increase or decrease the size of the triceps surae H-reflex in response to an operant conditioning task. This conditioning modifies the spinal cord. To determine the location and nature of the spinal cord plasticity and define its role in the behavioral change (i.e., H-reflex increase or decrease) we have recorded intracellularly from triceps surae motoneurons in conditioned animals and compared the results with data from naive (i.e., unconditioned) animals. 2. Eleven monkeys (Macaca nemestrina, male) were exposed to the HRdown conditioning mode, in which reward occurred when H-reflex size in one leg (i.e., the trained leg) was below a criterion value. In six animals (5.1-8.2 kg) H-reflex size in the trained leg fell to 24-58% of its initial value, whereas in the other five animals (4.0-5.5 kg) it remained at 92-114% of its initial value. This outcome, which was in accord with recent data indicating that success in HRdown conditioning is age dependent, allowed comparison of intracellular data from successful HRdown animals with data from unsuccessful animals as well as with data from naive (i.e., unconditioned) animals. 3. Intracellular recordings were obtained from 221 triceps surae motoneurons on trained and control sides of successful and unsuccessful HRdown animals. Measurements included axonal conduction velocity, input resistance, time constant, electrotonic length, rheobase, firing threshold, afterhyperpolarization duration and amplitude, and composite homonymous and heteronymous excitatory postsynaptic potentials to peripheral nerve stimulation. Results were compared with data from 109 triceps surae motoneurons in naive animals. 4. Motoneurons from the trained side of successful HRdown animals had a significantly more positive average firing threshold (-52 vs. -55 mV) and a significantly lower average conduction velocity (67 vs. 71 m/s) than those from naive animals. In contrast, motoneurons from the trained side of unsuccessful HRdown animals were not significantly different from naive motoneurons. 5. These data are consistent with the hypothesis that operantly conditioned decrease in H-reflex size is due to a positive shift in motoneuron firing threshold and a consequent increase in the depolarization needed to reach that threshold. 6. The more positive firing threshold, if present in the axon as well as in the soma, could also account for the decreased conduction velocity observed in motoneurons from the trained side of successful animals.
This article has been cited by other articles:
![]() |
X. Y. Chen, S. Pillai, Y. Chen, Y. Wang, L. Chen, J. S. Carp, and J. R. Wolpaw Spinal and Supraspinal Effects of Long-Term Stimulation of Sensorimotor Cortex in Rats J Neurophysiol, August 1, 2007; 98(2): 878 - 887. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. P. Zehr Training-induced adaptive plasticity in human somatosensory reflex pathways J Appl Physiol, December 1, 2006; 101(6): 1783 - 1794. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. L. Adkins, J. Boychuk, M. S. Remple, and J. A. Kleim Motor training induces experience-specific patterns of plasticity across motor cortex and spinal cord J Appl Physiol, December 1, 2006; 101(6): 1776 - 1782. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Stephens, J. Davidson, J. DeRosa, M. Kriz, and N. Saltzman Lengthening the Hamstring Muscles Without Stretching Using "Awareness Through Movement" Physical Therapy, December 1, 2006; 86(12): 1641 - 1650. [Abstract] [Full Text] [PDF] |
||||
![]() |
X. Y. Chen, L. Chen, Y. Chen, and J. R. Wolpaw Operant Conditioning of Reciprocal Inhibition in Rat Soleus Muscle J Neurophysiol, October 1, 2006; 96(4): 2144 - 2150. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. S. Carp, A. M. Tennissen, X. Y. Chen, and J. R. Wolpaw H-Reflex Operant Conditioning in Mice J Neurophysiol, October 1, 2006; 96(4): 1718 - 1727. [Abstract] [Full Text] [PDF] |
||||
![]() |
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 J Neurophysiol, July 1, 2006; 96(1): 119 - 127. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. R. Wolpaw and X. Y. Chen The cerebellum in maintenance of a motor skill: A hierarchy of brain and spinal cord plasticity underlies H-reflex conditioning. Learn. Mem., March 1, 2006; 13(2): 208 - 215. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. A Perez, B. K. S Lungholt, and J. B Nielsen Presynaptic control of group Ia afferents in relation to acquisition of a visuo-motor skill in healthy humans J. Physiol., October 1, 2005; 568(1): 343 - 354. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Chen, X. Y. Chen, L. B. Jakeman, G. Schalk, B. T. Stokes, and J. R. Wolpaw The Interaction of a New Motor Skill and an Old One: H-Reflex Conditioning and Locomotion in Rats J. Neurosci., July 20, 2005; 25(29): 6898 - 6906. [Abstract] [Full Text] [PDF] |
||||
![]() |
X. Y. Chen and J. R. Wolpaw Ablation of cerebellar nuclei prevents H-reflex down-conditioning in rats Learn. Mem., May 1, 2005; 12(3): 248 - 254. [Abstract] [Full Text] [PDF] |
||||
![]() |
X. Y. Chen, L. Chen, and J. R. Wolpaw Conditioned H-Reflex Increase Persists After Transection of the Main Corticospinal Tract in Rats J Neurophysiol, November 1, 2003; 90(5): 3572 - 3578. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. R. Wolpaw Memory in neuroscience: rhetoric versus reality. Behav Cogn Neurosci Rev, June 1, 2002; 1(2): 130 - 163. [Abstract] [PDF] |
||||
![]() |
P. Aagaard, E. B. Simonsen, J. L. Andersen, P. Magnusson, and P. Dyhre-Poulsen Neural adaptation to resistance training: changes in evoked V-wave and H-reflex responses J Appl Physiol, June 1, 2002; 92(6): 2309 - 2318. [Abstract] [Full Text] [PDF] |
||||
![]() |
X. Y. Chen and J. R. Wolpaw Probable Corticospinal Tract Control of Spinal Cord Plasticity in the Rat J Neurophysiol, February 1, 2002; 87(2): 645 - 652. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. D de Leon, R. R Roy, and V R. Edgerton Is the Recovery of Stepping Following Spinal Cord Injury Mediated by Modifying Existing Neural Pathways or by Generating New Pathways? A Perspective Physical Therapy, December 1, 2001; 81(12): 1904 - 1911. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Karl, N. Birbaumer, W. Lutzenberger, L. G. Cohen, and H. Flor Reorganization of Motor and Somatosensory Cortex in Upper Extremity Amputees with Phantom Limb Pain J. Neurosci., May 15, 2001; 21(10): 3609 - 3618. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. C. Field-Fote Spinal Cord Control of Movement: Implications for Locomotor Rehabilitation Following Spinal Cord Injury Physical Therapy, May 1, 2000; 80(5): 477 - 484. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Nargeot, D. A. Baxter, and J. H. Byrne In Vitro Analog of Operant Conditioning in Aplysia. I. Contingent Reinforcement Modifies the Functional Dynamics of an Identified Neuron J. Neurosci., March 15, 1999; 19(6): 2247 - 2260. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. J. Whelan and K. G. Pearson Plasticity in Reflex Pathways Controlling Stepping in the Cat J Neurophysiol, September 1, 1997; 78(3): 1643 - 1650. [Abstract] [Full Text] [PDF] |
||||
![]() |
X. Y. Chen and J. R. Wolpaw Dorsal Column But Not Lateral Column Transection Prevents Down-Conditioning of H Reflex in Rats J Neurophysiol, September 1, 1997; 78(3): 1730 - 1734. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |