Evidence map›Paper›PMID 27535367›Full record

ArticleJournal of neurophysiology2016

The inferior olive is essential for long-term maintenance of a simple motor skill.

Xiang Yang Chen, Yu Wang, Yi Chen, Lu Chen, Jonathan R Wolpaw

Abstract read
In one paragraph

Article in Journal of neurophysiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Suprapontine Structures Modulate Brainstem and Spinal Networks.Cellular and molecular neurobiology · 2023
    Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
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

5 authors.

Xiang Yang ChenNational Center for Adaptive Neurotechnologies, Wadsworth Center, New York State Department of Health, Albany, New York; xiangyang.chen@health.ny.gov.
Yu WangNational Center for Adaptive Neurotechnologies, Wadsworth Center, New York State Department of Health, Albany, New York.
Yi ChenNational Center for Adaptive Neurotechnologies, Wadsworth Center, New York State Department of Health, Albany, New York.
Lu ChenNational Center for Adaptive Neurotechnologies, Wadsworth Center, New York State Department of Health, Albany, New York.
Jonathan R WolpawNational Center for Adaptive Neurotechnologies, Wadsworth Center, New York State Department of Health, Albany, New York.

Funding

Training and DisseminationP41EB018783 · NIBIB · WADSWORTH CENTER · PI Jonathan Rickel Wolpaw · 2014 to 2026
$15.4M
BLRD VA I01 BX002550NIBIB NIH HHS P41 EB018783
6 · The paper itself

Abstract

The inferior olive (IO) is essential for operant down-conditioning of the rat soleus H-reflex, a simple motor skill. To evaluate the role of the IO in long-term maintenance of this skill, the H-reflex was down-conditioned over 50 days, the IO was chemically ablated, and down-conditioning continued for up to 102 more days. H-reflex size just before IO ablation averaged 62(±2 SE)% of its initial value (P < 0.001 vs. initial). After IO ablation, H-reflex size rose to 75-80% over ∼10 days, remained there for ∼30 days, rose over 10 days to above its initial value, and averaged 140(±14)% for the final 10 days of study (P < 0.01 vs. initial). This two-stage loss of down-conditioning maintenance correlated with IO neuronal loss (r = 0.75, P < 0.01) and was similar to the loss of down-conditioning that follows ablation of the cerebellar output nuclei dentate and interpositus. In control (i.e., unconditioned) rats, IO ablation has no long-term effect on H-reflex size. These results indicate that the IO is essential for long-term maintenance of a down-conditioned H-reflex. With previous data, they support the hypothesis that IO and cortical inputs to cerebellum combine to produce cerebellar plasticity that produces sensorimotor cortex plasticity that produces spinal cord plasticity that produces the smaller H-reflex. H-reflex down-conditioning appears to depend on a hierarchy of plasticity that may be guided by the IO and begin in the cerebellum. Similar hierarchies may underlie other motor learning.

Indexed as

Analysis of VarianceAnimalsCerebellumConditioning, OperantElectrodes, ImplantedElectromyographyH-ReflexMaleMemoryMotor SkillsMuscle, SkeletalNeuronal PlasticityOlivary NucleusRats, Sprague-DawleySpinal CordcerebellumH-reflexlearningmemoryoperant conditioningplasticitysensorimotor cortexspinal cord

Identifiers

PMID27535367
PMCPMC5144694

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.