Evidence map›Paper›PMID 25787951›Full record

ArticleJournal of neurophysiology2015

Compensatory plasticity restores locomotion after chronic removal of descending projections.

Cynthia M Harley, Melissa G Reilly, Christopher Stewart, Chantel Schlegel, Emma Morley, Joshua G Puhl, Christian Nagel, Kevin M Crisp, Karen A Mesce

Open access · greenAbstract read
In one paragraph

Article in Journal of neurophysiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.0field-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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Developmental Disruption of Recurrent Inhibitory Feedback Results in Compensatory Adaptation in the Renshaw Cell-Motor Neuron Circuit.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Cynthia M HarleyDepartment of Entomology, University of Minnesota, Saint Paul, Minnesota;
Melissa G ReillyDepartment of Entomology, University of Minnesota, Saint Paul, Minnesota;
Christopher StewartDepartment of Biology and Neuroscience Program, Saint Olaf College, Northfield, Minnesota.
Chantel SchlegelDepartment of Entomology, University of Minnesota, Saint Paul, Minnesota;
Emma MorleyDepartment of Entomology, University of Minnesota, Saint Paul, Minnesota;
Joshua G PuhlGraduate Program in Neuroscience, University of Minnesota, Saint Paul, Minnesota; and.
Christian NagelDepartment of Entomology, University of Minnesota, Saint Paul, Minnesota;
Kevin M CrispDepartment of Biology and Neuroscience Program, Saint Olaf College, Northfield, Minnesota.
Karen A MesceDepartment of Entomology, University of Minnesota, Saint Paul, Minnesota; Graduate Program in Neuroscience, University of Minnesota, Saint Paul, Minnesota; and mesce001@umn.edu.
University of Minnesota · USSt. Olaf College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Homeostatic plasticity is an important attribute of neurons and their networks, enabling functional recovery after perturbation. Furthermore, the directed nature of this plasticity may hold a key to the restoration of locomotion after spinal cord injury. Here we studied the recovery of crawling in the leech Hirudo verbana after descending cephalic fibers were surgically separated from crawl central pattern generators shown previously to be regulated by dopamine. We observed that immediately after nerve cord transection leeches were unable to crawl, but remarkably, after a day to weeks, animals began to show elements of crawling and intersegmental coordination. Over a similar time course, excessive swimming due to the loss of descending inhibition returned to control levels. Additionally, removal of the brain did not prevent crawl recovery, indicating that connectivity of severed descending neurons was not essential. After crawl recovery, a subset of animals received a second transection immediately below the anterior-most ganglion remaining. Similar to their initial transection, a loss of crawling with subsequent recovery was observed. These data, in recovered individuals, support the idea that compensatory plasticity directly below the site of injury is essential for the initiation and coordination of crawling. We maintain that the leech provides a valuable model to understand the neural mechanisms underlying locomotor recovery after injury because of its experimental accessibility, segmental organization, and dependence on higher-order control involved in the initiation, modulation, and coordination of locomotor behavior.

Indexed as

Afferent PathwaysAnimalsLitchiLocomotionMotor NeuronsNerve RegenerationNeuronal PlasticityPsychomotor PerformanceRecovery of FunctionTime Factorscentral pattern generatorcrawlingdopaminehomeostatic plasticitylocomotion

Identifiers

PMID25787951
PMCPMC4461884
OpenAlexW2053542717

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.