Evidence map›Paper›PMID 25789848›Full record

ArticleJournal of neuroscience research2015

Spinal neuronal activation during locomotor-like activity enabled by epidural stimulation and 5-hydroxytryptamine agonists in spinal rats.

Paul O Duru, Niranjala J K Tillakaratne, Jung A Kim, Hui Zhong, Stacey M Stauber, Trinh T Pham, Mei S Xiao, V Reggie Edgerton, Roland R Roy

Abstract read
In one paragraph

Article in Journal of neuroscience research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. 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

9 authors.

Paul O DuruDepartment of Integrative Biology and Physiology, University of California, Los Angeles, Los Angeles, California.
Niranjala J K TillakaratneDepartment of Integrative Biology and Physiology, University of California, Los Angeles, Los Angeles, California.
Jung A KimDepartment of Integrative Biology and Physiology, University of California, Los Angeles, Los Angeles, California.
Hui ZhongDepartment of Integrative Biology and Physiology, University of California, Los Angeles, Los Angeles, California.
Stacey M StauberDepartment of Integrative Biology and Physiology, University of California, Los Angeles, Los Angeles, California.
Trinh T PhamDepartment of Integrative Biology and Physiology, University of California, Los Angeles, Los Angeles, California.
Mei S XiaoDepartment of Integrative Biology and Physiology, University of California, Los Angeles, Los Angeles, California.
V Reggie EdgertonDepartment of Integrative Biology and Physiology, University of California, Los Angeles, Los Angeles, California.
Roland R RoyDepartment of Integrative Biology and Physiology, University of California, Los Angeles, Los Angeles, California.

Funding

USE DEPENDENT MOLECULAR MODULATION OF RAT HINDLIMB MUSCLESP01NS016333 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI HARKEMA, SUSAN J · 1985 to 2007
$9.9M
NINDS NIH HHS NS16333NINDS NIH HHS P01 NS016333
6 · The paper itself

Abstract

unlabelledThe neural networks that generate stepping in complete spinal adult rats remain poorly defined. To address this problem, we used c-fos (an activity-dependent marker) to identify active interneurons and motoneurons in the lumbar spinal cord of adult spinal rats during a 30-min bout of bipedal stepping. Spinal rats were either step trained (30 min/day, 3 days/week, for 7.5 weeks) or not step trained. Stepping was enabled by epidural stimulation and the administration of the serotonergic agonists quipazine and 8-OHDPAT. A third group of spinal rats served as untreated (no stimulation, drugs, or stepping) controls. The numbers of activated cholinergic central canal cluster cells and partition neurons were higher in both step-trained and nontrained rats than in untreated rats and were higher in nontrained than in step-trained rats. The latter finding suggests that daily treatment with epidural stimulation plus serotonergic agonist treatment without step training enhances the excitability of a broader cholinergic interneuronal population than does step training. The numbers of activated interneurons in laminae II-VI of lumbar cross-sections were higher in both step-trained and nontrained rats than in untreated rats, and they were highest in step-trained rats. This finding suggests that this population of interneurons is responsive to epidural stimulation plus serotonergic treatment and that load-bearing induced when stepping has an additive effect. The numbers of activated motoneurons of all size categories were higher in the step-trained group than in the other two groups, reflecting a strong effect of loading on motoneuron recruitment. In general, these results indicate that the spinal networks for locomotion are similar with and without brain input. SIGNIFICANCE: We identified neurons within the spinal cord networks that are activated during assisted stepping in paraplegic rats. We stimulated the spinal cord and administered a drug to help the rats step. One group was trained to step and another was not trained. We observed a lower percentage of activated neurons in specific spinal cord regions in trained rats than in nontrained rats after a 1-hr stepping bout, suggesting that step training reduces activation of some types of spinal neurons. This observation indicates that training makes the spinal networks more efficient and suggests a "learning" phenomenon in the spinal cord without any brain input.

Indexed as

AnimalsCholinergic NeuronsElectric Stimulation TherapyEpidural SpaceFemaleInterneuronsMotor ActivityRatsRats, Sprague-DawleySerotonin Receptor AgonistsSpinal CordSpinal Cord InjuriesSerotonin Receptor Agonistscentral canal cluster cellsc-fospartition neuronsRRID: AB_2079751RRID: AB_2106765serotonergic agonists

Identifiers

PMID25789848
PMCPMC4478222

What OpenQuestion holds

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Registered trials

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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.