Evidence map›Paper›PMID 34379540›Full record

ArticleJournal of neurophysiology2021

Effect of spinal cord injury on neural encoding of spontaneous postural perturbations in the hindlimb sensorimotor cortex.

Jaimie B Dougherty, Gregory D Disse, Nathaniel R Bridges, Karen A Moxon

Open access · greenAbstract read
In one paragraph

Article in Journal of neurophysiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 43% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

4 authors at 3 institutions in 1 country.

Jaimie B DoughertySchool of Biomedical Engineering, Science and Health Systems, Drexel University, Philadelphia, Pennsylvania.ORCID 0000-0002-9192-9274
Gregory D DisseDepartment of Biomedical Engineering, University of California at Davis, Davis, California.ORCID 0000-0002-2235-5270
Nathaniel R BridgesAir Force Research Laboratory, Wright-Patterson Air Force Base, Dayton, Ohio.ORCID 0000-0001-9899-6165
Karen A MoxonSchool of Biomedical Engineering, Science and Health Systems, Drexel University, Philadelphia, Pennsylvania.ORCID 0000-0002-5790-097X
Drexel University · USUniversity of California, Davis · USWright-Patterson Air Force Base · US

Funding

UC Davis Clinical and Translational Science CenterUL1TR001860 · NCATS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI KENYON, NICHOLAS J., LYLES, COURTNEY REES · 2016 to 2025
$47.3M
Enhancing supraspinal plasticity to improve functional recovery after SCIR01NS096971 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI BETHEA, JOHN ROLAND, MOXON, KAREN A · 2016 to 2020
$3.0M
NCATS NIH HHS UL1 TR001860NINDS NIH HHS R01 NS096971
6 · The paper itself

Abstract

Supraspinal signals play a significant role in compensatory responses to postural perturbations. Although the cortex is not necessary for basic postural tasks in intact animals, its role in responding to unexpected postural perturbations after spinal cord injury (SCI) has not been studied. To better understand how SCI impacts cortical encoding of postural perturbations, the activity of single neurons in the hindlimb sensorimotor cortex (HLSMC) was recorded in the rat during unexpected tilts before and after a complete midthoracic spinal transection. In a subset of animals, limb ground reaction forces were also collected. HLSMC activity was strongly modulated in response to different tilt profiles. As the velocity of the tilt increased, more information was conveyed by the HLSMC neurons about the perturbation due to increases in both the number of recruited neurons and the magnitude of their responses. SCI led to attenuated and delayed hindlimb ground reaction forces. However, HLSMC neurons remained responsive to tilts after injury but with increased latencies and decreased tuning to slower tilts. Information conveyed by cortical neurons about the tilts was therefore reduced after SCI, requiring more cells to convey the same amount of information as before the transection. Given that reorganization of the hindlimb sensorimotor cortex in response to therapy after complete midthoracic SCI is necessary for behavioral recovery, this sustained encoding of information after SCI could be a substrate for the reorganization that uses sensory information from above the lesion to control trunk muscles that permit weight-supported stepping and postural control.

Indexed as

AnimalsBehavior, AnimalDisease Models, AnimalElectrophysiological PhenomenaHindlimbNeuronsPostural BalancePostureRatsRats, Long-EvansSensorimotor CortexSpinal Cord Injurieselectrophysiologyneural encodingpostureratspinal cord injury

Identifiers

PMID34379540
PMCPMC8782649
OpenAlexW3190696754

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.