|
|
||||||||
Journal of Neurophysiology, Vol 61, Issue 3 563-572, Copyright © 1989 by APS
ARTICLES |
J. R. Wolpaw and C. L. Lee
Wadsworth Center for Laboratories and Research, New York State Department of Health, Albany 12201.
1. Study of memory traces in higher animals requires experimental models possessing well-localized and technically accessible memory traces--plasticity responsible for behavioral change, not dependent on control from elsewhere, and open to detailed investigation. Our purpose has been to develop such a model based on the wholly spinal, largely monosynaptic path of the spinal stretch reflex. Previous studies described operant conditioning of this reflex and of its electrical analog, the H-reflex. In this study, we sought to determine whether conditioning causes changes in the spinal cord that affect the reflex and are not dependent on continued supraspinal influence, and thus qualify as memory traces. 2. Sixteen monkeys underwent chronic conditioning of the triceps surae H-reflex. Eight were rewarded for increasing H-reflex amplitude (HR increases mode), and eight were rewarded for decreasing it (HR decreases mode). In each animal, the other leg was an internal control. Over several months of conditioning, H-reflex amplitude in the conditioned leg rose in HR increases animals and fell in HR decreases animals. H-reflex amplitude in the control leg changed little. 3. After HR increases or HR decreases conditioning, each animal was deeply anesthetized and surgically prepared. The reflex response to supramaximal dorsal root stimulation was measured from the triceps surae nerve as percent of response to supramaximal ventral root stimulation, which was the maximum possible response. Data from both legs were collected before and for up to 3 days after thoracic (T9-10) cord transection. The animal remained deeply anesthetized throughout and was killed by overdose. 4. The reflex asymmetries produced by conditioning were still present several days after transection removed supraspinal influence: reflexes of HR increases animals were significantly larger in HR increases legs than in control legs and reflexes of HR decreases animals were significantly smaller in HR decreases legs than in control legs. 5. Reflex amplitude was much greater in the control legs of anesthetized HR decreases animals than in the control legs of anesthetized HR increases animals. 6. Chronic conditioning had at least two effects on the spinal cord. The first effect, task-appropriate reflex asymmetry, was evident both in the awake behaving animal and in the anesthetized transected animal. The second effect, larger control leg reflexes in HR decreases than in HR increases animals, was evident only in the anesthetized animal. By removing supraspinal control, anesthesia and transection revealed a previously hidden effect of conditioning.(ABSTRACT TRUNCATED AT 400 WORDS)
This article has been cited by other articles:
![]() |
G. Barriere, H. Leblond, J. Provencher, and S. Rossignol Prominent Role of the Spinal Central Pattern Generator in the Recovery of Locomotion after Partial Spinal Cord Injuries J. Neurosci., April 9, 2008; 28(15): 3976 - 3987. [Abstract] [Full Text] [PDF] |
||||
![]() |
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] |
||||
![]() |
J. R. Wolpaw Brain-computer interfaces as new brain output pathways J. Physiol., March 15, 2007; 579(3): 613 - 619. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. W. Grau, E. D. Crown, A. R. Ferguson, S. N. Washburn, M. A. Hook, and R. C. Miranda Instrumental learning within the spinal cord: underlying mechanisms and implications for recovery after injury. Behav Cogn Neurosci Rev, December 1, 2006; 5(4): 191 - 239. [Abstract] [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] |
||||
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
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] |
||||
![]() |
G. E. Loeb Asymmetry of Hindlimb Muscle Activity and Cutaneous Reflexes After Tendon Transfers in Kittens J Neurophysiol, December 1, 1999; 82(6): 3392 - 3405. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. D. De Leon, J. A. Hodgson, R. R. Roy, and V. R. Edgerton Retention of Hindlimb Stepping Ability in Adult Spinal Cats After the Cessation of Step Training J Neurophysiol, January 1, 1999; 81(1): 85 - 94. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. R. Mcintosh and F. Gonzalez-Lima Large-Scale Functional Connectivity in Associative Learning: Interrelations of the Rat Auditory, Visual, and Limbic Systems J Neurophysiol, December 1, 1998; 80(6): 3148 - 3162. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Chau, H. Barbeau, and S. Rossignol Early Locomotor Training With Clonidine in Spinal Cats J Neurophysiol, January 1, 1998; 79(1): 392 - 409. [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] |
||||
![]() |
L. Carrier, E. Brustein, and S. Rossignol Locomotion of the Hindlimbs After Neurectomy of Ankle Flexors in Intact and Spinal Cats: Model for the Study of Locomotor Plasticity J Neurophysiol, April 1, 1997; 77(4): 1979 - 1993. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |