Evidence map›Paper›PMID 38568869›Full record

ArticleThe Journal of physiology2024

Motor learning changes the axon initial segment of the spinal motoneuron.

Yu Wang, Yi Chen, Lu Chen, Bruce J Herron, Xiang Yang Chen, Jonathan R Wolpaw

Open access · hybridAbstract read
In one paragraph

Article in The Journal of physiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 30% of its field
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

4 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
  3. Relationship Between Spinal Reflexes and Spastic Movement Disorders.Physical medicine and rehabilitation clinics of North America · 2026
    Review
  4. Review
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

6 authors at 2 institutions in 1 country.

Yu WangNational Center for Adaptive Neurotechnologies, Albany Stratton VA Medical Center, Albany, NY, USA.
Yi ChenNational Center for Adaptive Neurotechnologies, Albany Stratton VA Medical Center, Albany, NY, USA.
Lu ChenNational Center for Adaptive Neurotechnologies, Albany Stratton VA Medical Center, Albany, NY, USA.
Bruce J HerronWadsworth Center, New York State Department of Health, Albany, NY, USA.ORCID 0000-0002-0233-9513
Xiang Yang ChenNational Center for Adaptive Neurotechnologies, Albany Stratton VA Medical Center, Albany, NY, USA.
Jonathan R WolpawNational Center for Adaptive Neurotechnologies, Albany Stratton VA Medical Center, Albany, NY, USA.ORCID 0000-0003-0805-1315
Albany State University · USNeurotech (United States) · US

Funding

Training and DisseminationP41EB018783 · NIBIB · WADSWORTH CENTER · PI Jonathan Saul Carp · 2014 to 2026
$15.4M
Spinal Effects of Cortical Stimulation: Mechanisms and Functional ImpactR01NS110577 · NINDS · WADSWORTH CENTER · PI CARP, JONATHAN SAUL, VATO, ALESSANDRO · 2019 to 2023
$4.1M
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
Dynamics and Causal Functions of Large-Scale Cortical and Subcortical NetworksU01NS108916 · NINDS · WADSWORTH CENTER · PI WOLPAW, JONATHAN RICKEL · 2018 to 2019
$1.4M
Spinal Reflex Conditioning and LocomotionR01NS061823 · NINDS · WADSWORTH CENTER · PI CHEN, XIANG YANG, WOLPAW, JONATHAN RICKEL · 2008 to 2011
$1.3M
Operant Conditioning of Spinal Reflexes to Improve Function after Nerve InjuryI01BX002550 · VA · STRATTON VETERANS ADMIN MEDICAL CENTER · PI WOLPAW, JONATHAN RICKEL · 2014 to 2017
–
BLRD VA I01 BX002550NIBIB NIH HHS P41 EB018783NICHD NIH HHS R01 HD036020NINDS NIH HHS R01 NS022189NINDS NIH HHS R01 NS061823NINDS NIH HHS R01 NS110577NINDS NIH HHS U01 NS108916
6 · The paper itself

Abstract

We are studying the mechanisms of H-reflex operant conditioning, a simple form of learning. Modelling studies in the literature and our previous data suggested that changes in the axon initial segment (AIS) might contribute. To explore this, we used blinded quantitative histological and immunohistochemical methods to study in adult rats the impact of H-reflex conditioning on the AIS of the spinal motoneuron that produces the reflex. Successful, but not unsuccessful, H-reflex up-conditioning was associated with greater AIS length and distance from soma; greater length correlated with greater H-reflex increase. Modelling studies in the literature suggest that these increases may increase motoneuron excitability, supporting the hypothesis that they may contribute to H-reflex increase. Up-conditioning did not affect AIS ankyrin G (AnkG) immunoreactivity (IR), p-p38 protein kinase IR, or GABAergic terminals. Successful, but not unsuccessful, H-reflex down-conditioning was associated with more GABAergic terminals on the AIS, weaker AnkG-IR, and stronger p-p38-IR. More GABAergic terminals and weaker AnkG-IR correlated with greater H-reflex decrease. These changes might potentially contribute to the positive shift in motoneuron firing threshold underlying H-reflex decrease; they are consistent with modelling suggesting that sodium channel change may be responsible. H-reflex down-conditioning did not affect AIS dimensions. This evidence that AIS plasticity is associated with and might contribute to H-reflex conditioning adds to evidence that motor learning involves both spinal and brain plasticity, and both neuronal and synaptic plasticity. AIS properties of spinal motoneurons are likely to reflect the combined influence of all the motor skills that share these motoneurons. KEY POINTS: Neuronal action potentials normally begin in the axon initial segment (AIS). AIS plasticity affects neuronal excitability in development and disease. Whether it does so in learning is unknown. Operant conditioning of a spinal reflex, a simple learning model, changes the rat spinal motoneuron AIS. Successful, but not unsuccessful, H-reflex up-conditioning is associated with greater AIS length and distance from soma. Successful, but not unsuccessful, down-conditioning is associated with more AIS GABAergic terminals, less ankyrin G, and more p-p38 protein kinase. The associations between AIS plasticity and successful H-reflex conditioning are consistent with those between AIS plasticity and functional changes in development and disease, and with those predicted by modelling studies in the literature. Motor learning changes neurons and synapses in spinal cord and brain. Because spinal motoneurons are the final common pathway for behaviour, their AIS properties probably reflect the combined impact of all the behaviours that use these motoneurons.

Indexed as

Axon Initial SegmentH-ReflexMotor NeuronsRats, Sprague-DawleyAnimalsAnkyrinsAxonsConditioning, OperantLearningMaleNeuronal PlasticityRatsSpinal CordAnkyrinsactivity‐dependent plasticityaxon initial segment (AIS)heksorH‐reflexmotor learningnegotiated equilibriumoperant conditioningspinal motoneuron

Identifiers

PMID38568869
PMCPMC11196014
OpenAlexW4393869048

What OpenQuestion holds

Textmetadata
LicenceTDM
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.