Evidence map›Paper›PMID 27306676›Full record

ArticleJournal of neurophysiology2016

Self-reinnervated muscles lose autogenic length feedback, but intermuscular feedback can recover functional connectivity.

Mark A Lyle, Boris I Prilutsky, Robert J Gregor, Thomas A Abelew, T Richard Nichols

Open access · greenAbstract 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 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. 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
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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

5 authors at 3 institutions in 1 country.

Mark A LyleSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, Georgia; mlyle@ap.gatech.edu.
Boris I PrilutskySchool of Biological Sciences, Georgia Institute of Technology, Atlanta, Georgia;
Robert J GregorSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, Georgia; Division of Biokinesiology and Physical Therapy, University of Southern California, Los Angeles, California; and.
Thomas A AbelewSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, Georgia; Department of Cell Biology, Emory University, Atlanta, Georgia.
T Richard NicholsSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, Georgia;
Georgia Institute of Technology · USEmory University · USUniversity of Southern California · US

Funding

Influence of alpha-2 agonists on reflex pathways and limb stiffnessF32NS080393 · NINDS · GEORGIA INSTITUTE OF TECHNOLOGY · PI LYLE, MARK A · 2013 to 2015
$152k
NINDS NIH HHS F32 NS080393
6 · The paper itself

Abstract

In this study, we sought to identify sensory circuitry responsible for motor deficits or compensatory adaptations after peripheral nerve cut and repair. Self-reinnervation of the ankle extensor muscles abolishes the stretch reflex and increases ankle yielding during downslope walking, but it remains unknown whether this finding generalizes to other muscle groups and whether muscles become completely deafferented. In decerebrate cats at least 19 wk after nerve cut and repair, we examined the influence of quadriceps (Q) muscles' self-reinnervation on autogenic length feedback, as well as intermuscular length and force feedback, among the primary extensor muscles in the cat hindlimb. Effects of gastrocnemius and soleus self-reinnervation on intermuscular circuitry were also evaluated. We found that autogenic length feedback was lost after Q self-reinnervation, indicating that loss of the stretch reflex appears to be a generalizable consequence of muscle self-reinnervation. However, intermuscular force and length feedback, evoked from self-reinnervated muscles, was preserved in most of the interactions evaluated with similar relative inhibitory or excitatory magnitudes. These data indicate that intermuscular spinal reflex circuitry has the ability to regain functional connectivity, but the restoration is not absolute. Explanations for the recovery of intermuscular feedback are discussed, based on identified mechanisms responsible for lost autogenic length feedback. Functional implications, due to permanent loss of autogenic length feedback and potential for compensatory adaptations from preserved intermuscular feedback, are discussed.

Indexed as

AnimalsAnkle JointCatsDisease Models, AnimalElectromyographyEvoked Potentials, MotorFeedback, SensoryFemaleHindlimbMuscle ContractionMuscle, SkeletalPeripheral Nerve InjuriesRecovery of FunctionReflex, Stretchforce feedbackGolgi tendon organmuscle self-reinnervationstretch reflex

Identifiers

PMID27306676
PMCPMC5009216
OpenAlexW2440657268

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.