Activity-dependent spinal cord plasticity affects motor function in health and disease. It contributes to skill acquisition, underlies the abnormal function associated with spinal cord injury, and should be a key factor in the design of effective new therapies. Yet this plasticity and the processes that create it are not understood. Progress requires a simple laboratory model in which it is possible to identify the sites and explore the mechanisms of activity-dependent spinal cord plasticity and to describe its translation into behavior. The spinal stretch reflex (SSR), or tendon jerk, which is mediated by a wholly spinal and largely monosynaptic pathway, is a model that satisfies these requirements. Because this spinal pathway is influenced by descending activity from the brain, monkeys, humans, and rats can gradually increase or decrease the SSR or its electrical analog, the H-reflex, in response to an operant conditioning paradigm. The learning changes the spinal cord, since evidence of it remains even after all descending activity is removed. This laboratory is defining the complex activity-dependent spinal cord plasticity underlying this simple change in motor function, the mechanisms that create the plasticity, and the manner in which it translates into behavior. The central hypotheses, supported by previous results and preliminary data, are: (1) that the complex spinal cord plasticity produced by H-reflex conditioning affects other spinal cord reflexes including reciprocal inhibition and presynaptic inhibition of agonist and antagonist muscles; (2) that the corticospinal tract, contralateral (and probably ipsilateral) sensorimotor cortex, and cerebellar-cortical connections are essential for acquisition and maintenance of this spinal cord plasticity; and (3) that this spinal cord plasticity affects spinal cord function during locomotion. These hypotheses will be tested by studying the effects of H-reflex conditioning on other spinal cord reflexes, by studying the effects of specific supraspinal lesions on H-reflex conditioning, and by studying the effects of H-reflex conditioning on responses to calibrated afferent inputs during locomotion. The results should lead to new understanding of the complex plasticity underlying the acquisition of motor skills and the changes in spinal cord function associated with trauma and disease, and should contribute to the development and assessment of new methods for improving function after spinal cord injury.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
2R01NS022189-16A1
Application #
6479696
Study Section
Integrative, Functional and Cognitive Neuroscience 8 (IFCN)
Program Officer
Kleitman, Naomi
Project Start
1985-04-01
Project End
2007-02-28
Budget Start
2002-03-01
Budget End
2003-02-28
Support Year
16
Fiscal Year
2002
Total Cost
$337,351
Indirect Cost
Name
Wadsworth Center
Department
Type
DUNS #
110521739
City
Menands
State
NY
Country
United States
Zip Code
12204
Eftekhar, Amir; Norton, James J S; McDonough, Christine M et al. (2018) Retraining Reflexes: Clinical Translation of Spinal Reflex Operant Conditioning. Neurotherapeutics :
Norton, James J S; Wolpaw, Jonathan R (2018) Acquisition, Maintenance, and Therapeutic Use of a Simple Motor Skill. Curr Opin Behav Sci 20:138-144
LaPallo, Brandon K; Wolpaw, Jonathan R; Yang Chen, Xiang et al. (2017) Spinal Transection Alters External Urethral Sphincter Activity during Spontaneous Voiding in Freely Moving Rats. J Neurotrauma 34:3012-3026
Chen, Yi; Chen, Lu; Wang, Yu et al. (2017) Why New Spinal Cord Plasticity Does Not Disrupt Old Motor Behaviors. J Neurosci 37:8198-8206
Chen, Xiang Yang; Wang, Yu; Chen, Yi et al. (2016) Ablation of the inferior olive prevents H-reflex down-conditioning in rats. J Neurophysiol 115:1630-6
LaPallo, Brandon K; Wolpaw, Jonathan R; Chen, Xiang Yang et al. (2016) Contribution of the external urethral sphincter to urinary void size in unanesthetized unrestrained rats. Neurourol Urodyn 35:696-702
Thompson, Aiko K; Wolpaw, Jonathan R (2015) Targeted neuroplasticity for rehabilitation. Prog Brain Res 218:157-72
Boulay, Chadwick B; Chen, Xiang Yang; Wolpaw, Jonathan R (2015) Electrocorticographic activity over sensorimotor cortex and motor function in awake behaving rats. J Neurophysiol 113:2232-41
Thompson, Aiko K; Wolpaw, Jonathan R (2015) Restoring walking after spinal cord injury: operant conditioning of spinal reflexes can help. Neuroscientist 21:203-15
Thompson, Aiko K; Wolpaw, Jonathan R (2014) The simplest motor skill: mechanisms and applications of reflex operant conditioning. Exerc Sport Sci Rev 42:82-90

Showing the most recent 10 out of 91 publications