Evidence map›Paper›PMID 16585796›Full record

ArticleLearning & memory (Cold Spring Harbor, N.Y.)

The cerebellum in maintenance of a motor skill: a hierarchy of brain and spinal cord plasticity underlies H-reflex conditioning.

Jonathan R Wolpaw, Xiang Yang Chen

Open access · diamondAbstract readComparative Study
In one paragraph

Article in Learning & memory (Cold Spring Harbor, N.Y.). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
  2. Relationship Between Spinal Reflexes and Spastic Movement Disorders.Physical medicine and rehabilitation clinics of North America · 2026
    Review
  3. Article
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  11. Retraining Reflexes: Clinical Translation of Spinal Reflex Operant Conditioning.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2018
    Review
  12. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 2 institutions in 1 country.

Jonathan R WolpawLaboratory of Nervous System Disorders Wadsworth Center, New York State Department of Health and State University of New York at Albany, Albany, New York 12201-0509, USA. wolpaw@wadsworth.org
Xiang Yang Chen
New York State Department of Health · USWadsworth Center · US

Funding

SUPRASPINAL CONTROL OF SPINAL CORD PLASTICITYR01HD036020 · NICHD · WADSWORTH CENTER · PI CHEN, XIANG YANG · 1997 to 2012
$3.2M
ADAPTIVE PLASTICITY IN THE SPINAL STRETCH REFLEXR01NS022189 · NINDS · WADSWORTH CENTER · PI WOLPAW, JONATHAN RICKEL · 1985 to 2012
$3.1M
NICHD NIH HHS HD36020NICHD NIH HHS R01 HD036020NINDS NIH HHS NS22189NINDS NIH HHS R01 NS022189
6 · The paper itself

Abstract

Operant conditioning of the H-reflex, the electrical analog of the spinal stretch reflex, is a simple model of skill acquisition and involves plasticity in the spinal cord. Previous work showed that the cerebellum is essential for down-conditioning the H-reflex. This study asks whether the cerebellum is also essential for maintaining down-conditioning. After rats decreased the soleus H-reflex over 50 d in response to the down-conditioning protocol, the cerebellar output nuclei dentate and interpositus (DIN) were ablated, and down-conditioning continued for 50-100 more days. In naive (i.e., unconditioned) rats, DIN ablation itself has no significant long-term effect on H-reflex size. During down-conditioning prior to DIN ablation, eight Sprague-Dawley rats decreased the H-reflex to 57% (+/-4 SEM) of control. It rose after ablation, stabilizing within 2 d at about 75% and remaining there until approximately 40 d after ablation. It then rose to approximately 130%, where it remained through the end of study 100 d after ablation. Thus, DIN ablation in down-conditioned rats caused an immediate increase and a delayed increase in the H-reflex. The final result was an H-reflex significantly larger than that prior to down-conditioning. Combined with previous work, these remarkable results suggest that the spinal cord plasticity directly responsible for down-conditioning, which survives only 5-10 d on its own, is maintained by supraspinal plasticity that survives approximately 40 d after loss of cerebellar output. Thus, H-reflex conditioning seems to depend on a hierarchy of brain and spinal cord plasticity to which the cerebellum makes an essential contribution.

Indexed as

AnimalsAssociation LearningBrainCerebellar NucleiCerebellumConditioning, ClassicalFemaleH-ReflexMaleMotor SkillsNeural PathwaysNeuronal PlasticityRatsRats, Sprague-DawleySpinal Cord

Identifiers

PMID16585796
PMCPMC1409832
OpenAlexW2102036778

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.