Evidence map›Paper›PMID 37499972›Full record

ArticleExperimental neurology2023

Spinal control of locomotion before and after spinal cord injury.

Simon M Danner, Courtney T Shepard, Casey Hainline, Natalia A Shevtsova, Ilya A Rybak, David S K Magnuson

Abstract read
In one paragraph

Article in Experimental neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Simon M DannerDepartment of Neurobiology and Anatomy, College of Medicine, Drexel University, Philadelphia, PA, USA. Electronic address: smd395@drexel.edu.
Courtney T ShepardInterdisciplinary Program in Translational Neuroscience, University of Louisville School of Medicine, Health Sciences Campus, Louisville, KY, USA.
Casey HainlineSpeed School of Engineering, University of Louisville School of Medicine, Health Sciences Campus, Louisville, KY, USA.
Natalia A ShevtsovaDepartment of Neurobiology and Anatomy, College of Medicine, Drexel University, Philadelphia, PA, USA.
Ilya A RybakDepartment of Neurobiology and Anatomy, College of Medicine, Drexel University, Philadelphia, PA, USA.
David S K MagnusonDepartment of Neurological Surgery, University of Louisville School of Medicine, Health Sciences Campus, Louisville, KY, USA; Kentucky Spinal Cord Injury Research Center, University of Louisville School of Medicine, Health Sciences Campus, Louisville, KY, USA.

Funding

Limb coordination during locomotion before and after spinal cord injuryR01NS110550 · NINDS · GEORGIA INSTITUTE OF TECHNOLOGY · PI BORIS I PRILUTSKY, Ilya A Rybak · 2020 to 2026
$3.9M
Propriopsinal neuron function in normal and post-SCI locomotionR01NS112304 · NINDS · UNIVERSITY OF LOUISVILLE · PI Simon Michael Danner, David SK Magnuson · 2021 to 2026
$3.0M
Functional consequences of silencing propriospinal pathways after SCI in the adult ratR01NS089324 · NINDS · UNIVERSITY OF LOUISVILLE · PI MAGNUSON, DAVID SK, WHITTEMORE, SCOTT R · 2015 to 2019
$2.0M
Spinal circuits for sensorimotor integration and interlimb coordination during locomotionR01NS115900 · NINDS · DREXEL UNIVERSITY · PI DANNER, SIMON MICHAEL · 2020 to 2024
$1.7M
NINDS NIH HHS R01 NS089324NINDS NIH HHS R01 NS110550NINDS NIH HHS R01 NS112304NINDS NIH HHS R01 NS115900
6 · The paper itself

Abstract

Thoracic spinal cord injury affects long propriospinal neurons that interconnect the cervical and lumbar enlargements. These neurons are crucial for coordinating forelimb and hindlimb locomotor movements in a speed-dependent manner. However, recovery from spinal cord injury is usually studied over a very limited range of speeds that may not fully expose circuitry dysfunction. To overcome this limitation, we investigated overground locomotion in rats trained to move over an extended distance with a wide range of speeds both pre-injury and after recovery from thoracic hemisection or contusion injuries. In this experimental context, intact rats expressed a speed-dependent continuum of alternating (walk and trot) and non-alternating (canter, gallop, half-bound gallop, and bound) gaits. After a lateral hemisection injury, rats recovered the ability to locomote over a wide range of speeds but lost the ability to use the highest-speed gaits (half-bound gallop and bound) and predominantly used the limb contralateral to the injury as lead during canter and gallop. A moderate contusion injury caused a greater reduction in maximal speed, loss of all non-alternating gaits, and emergence of novel alternating gaits. These changes resulted from weak fore-hind coupling together with appropriate control of left-right alternation. After hemisection, animals expressed a subset of intact gaits with appropriate interlimb coordination even on the side of the injury, where the long propriospinal connections were severed. These observations highlight how investigating locomotion over the full range of speeds can reveal otherwise hidden aspects of spinal locomotor control and post-injury recovery.

Indexed as

ContusionsSpinal Cord InjuriesAnimalsGaitHindlimbLocomotionRatsSpinal CordContusionHemisectionInterlimb coordinationLocomotionLong propriospinal neuronsSpinal cord injurySpinal locomotor circuitry

Identifiers

PMID37499972
PMCPMC10529867

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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.