Evidence map›Paper›PMID 34797870›Full record

ArticlePloS one2021

Axon initial segment geometry in relation to motoneuron excitability.

Travis M Rotterman, Darío I Carrasco, Stephen N Housley, Paul Nardelli, Randall K Powers, Timothy C Cope

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
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  4. Review
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  8. Structural Preservation Does Not Ensure Function at Sensory Ia-Motoneuron Synapses following Peripheral Nerve Injury and Repair.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  9. 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

6 authors at 2 institutions in 1 country.

Travis M RottermanSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, United States of America.ORCID 0000-0003-0044-7948
Darío I CarrascoSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, United States of America.
Stephen N HousleySchool of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, United States of America.
Paul NardelliSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, United States of America.
Randall K PowersDepartment of Physiology and Biophysics, University of Washington, Seattle, WA, United States of America.
Timothy C CopeSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, United States of America.
Georgia Institute of Technology · USUniversity of Washington · US

Funding

Novel Path to Chronic Sensorimotor Dysfunction and Treatment for ChemotherapyR01CA221363 · NCI · GEORGIA INSTITUTE OF TECHNOLOGY · PI COPE, TIMOTHY C · 2018 to 2022
$1.5M
Preservation of sensory la afferent boutons on motoneurons after peripheral nerve injury restores synaptic transmissions and rescues whole limb kinematicsF32NS112556 · NINDS · GEORGIA INSTITUTE OF TECHNOLOGY · PI ROTTERMAN, TRAVIS MICHAEL · 2019 to 2021
$160k
NCI NIH HHS R01 CA221363NINDS NIH HHS F32 NS112556
6 · The paper itself

Abstract

The axon initial segment (AIS) responsible for action potential initiation is a dynamic structure that varies and changes together with neuronal excitability. Like other neuron types, alpha motoneurons in the mammalian spinal cord express heterogeneity and plasticity in AIS geometry, including length (AISl) and distance from soma (AISd). The present study aimed to establish the relationship of AIS geometry with a measure of intrinsic excitability, rheobase current, that varies by 20-fold or more among normal motoneurons. We began by determining whether AIS length or distance differed for motoneurons in motor pools that exhibit different activity profiles. Motoneurons sampled from the medial gastrocnemius (MG) motor pool exhibited values for average AISd that were significantly greater than that for motoneurons from the soleus (SOL) motor pool, which is more readily recruited in low-level activities. Next, we tested whether AISd covaried with intrinsic excitability of individual motoneurons. In anesthetized rats, we measured rheobase current intracellularly from MG motoneurons in vivo before labeling them for immunohistochemical study of AIS structure. For 16 motoneurons sampled from the MG motor pool, this combinatory approach revealed that AISd, but not AISl, was significantly related to rheobase, as AIS tended to be located further from the soma on motoneurons that were less excitable. Although a causal relation with excitability seems unlikely, AISd falls among a constellation of properties related to the recruitability of motor units and their parent motoneurons.

Indexed as

Action PotentialsAnimalsAxon Initial SegmentAxonsElectrophysiologyMaleMotor NeuronsMusclesNeural ConductionNeurons, EfferentRatsRats, WistarSpinal Cord

Identifiers

PMID34797870
PMCPMC8604372
OpenAlexW3211656378

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.