Evidence map›Paper›PMID 26713446›Full record

ArticlePloS one2015

Thoracic 9 Spinal Transection-Induced Model of Muscle Spasticity in the Rat: A Systematic Electrophysiological and Histopathological Characterization.

Jose A Corleto, Mariana Bravo-Hernández, Kota Kamizato, Osamu Kakinohana, Camila Santucci, Michael R Navarro, Oleksandr Platoshyn, Dasa Cizkova, Nadezda Lukacova, Julian Taylor and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  4. Review
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  6. MicroRNA-34a: the bad guy in age-related vascular diseases.Cellular and molecular life sciences : CMLS · 2021
    Review
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  9. The Involvement of CaFrontiers in neural circuits · 2021
    Article
  10. Article
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  14. Neuropathic Pain After Spinal Cord Injury: Challenges and Research Perspectives.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2018
    Review
  15. Review
  16. Review
  17. Article
  18. 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

11 authors at 3 institutions in 4 countries.

Jose A CorletoNeuroregeneration Laboratory, Department of Anesthesiology, University of California - San Diego, La Jolla, California, United States of America.
Mariana Bravo-HernándezNeuroregeneration Laboratory, Department of Anesthesiology, University of California - San Diego, La Jolla, California, United States of America.
Kota KamizatoNeuroregeneration Laboratory, Department of Anesthesiology, University of California - San Diego, La Jolla, California, United States of America.
Osamu KakinohanaNeuroregeneration Laboratory, Department of Anesthesiology, University of California - San Diego, La Jolla, California, United States of America.
Camila SantucciNeuroregeneration Laboratory, Department of Anesthesiology, University of California - San Diego, La Jolla, California, United States of America.
Michael R NavarroNeuroregeneration Laboratory, Department of Anesthesiology, University of California - San Diego, La Jolla, California, United States of America.
Oleksandr PlatoshynNeuroregeneration Laboratory, Department of Anesthesiology, University of California - San Diego, La Jolla, California, United States of America.
Dasa CizkovaInstitute of Neurobiology, Slovak Academy of Sciences, Soltesovej 6, Kosice, Slovakia.
Nadezda LukacovaInstitute of Neurobiology, Slovak Academy of Sciences, Soltesovej 6, Kosice, Slovakia.
Julian TaylorHospital Nacional de Paraplejicos, SESCAM, Toledo, Spain.
Martin MarsalaNeuroregeneration Laboratory, Department of Anesthesiology, University of California - San Diego, La Jolla, California, United States of America.
University of California San Diego · USSlovak Academy of Sciences · SKServicio de Salud de Castilla La Mancha · ES

Funding

Ischemic Spasticity: Modulation by GAD65 Gene DeliveryR01NS051644 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MARSALA, MARTIN · 2006 to 2010
$1.8M
Ischemic Paraplegia: Modulation by Stem Cell ImplantR01NS040386 · NINDS · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI MARSALA, MARTIN · 2002 to 2005
$1.5M
NINDS NIH HHS NS40386NINDS NIH HHS NS51644NINDS NIH HHS R01 NS040386NINDS NIH HHS R01 NS051644
6 · The paper itself

Abstract

The development of spinal hyper-reflexia as part of the spasticity syndrome represents one of the major complications associated with chronic spinal traumatic injury (SCI). The primary mechanism leading to progressive appearance of muscle spasticity is multimodal and may include loss of descending inhibitory tone, alteration of segmental interneuron-mediated inhibition and/or increased reflex activity to sensory input. Here, we characterized a chronic thoracic (Th 9) complete transection model of muscle spasticity in Sprague-Dawley (SD) rats. Isoflurane-anesthetized rats received a Th9 laminectomy and the spinal cord was transected using a scalpel blade. After the transection the presence of muscle spasticity quantified as stretch and cutaneous hyper-reflexia was identified and quantified as time-dependent changes in: i) ankle-rotation-evoked peripheral muscle resistance (PMR) and corresponding electromyography (EMG) activity, ii) Hoffmann reflex, and iii) EMG responses in gastrocnemius muscle after paw tactile stimulation for up to 8 months after injury. To validate the clinical relevance of this model, the treatment potency after systemic treatment with the clinically established anti-spastic agents baclofen (GABAB receptor agonist), tizanidine (α2-adrenergic agonist) and NGX424 (AMPA receptor antagonist) was also tested. During the first 3 months post spinal transection, a progressive increase in ankle rotation-evoked muscle resistance, Hoffmann reflex amplitude and increased EMG responses to peripherally applied tactile stimuli were consistently measured. These changes, indicative of the spasticity syndrome, then remained relatively stable for up to 8 months post injury. Systemic treatment with baclofen, tizanidine and NGX424 led to a significant but transient suppression of spinal hyper-reflexia. These data demonstrate that a chronic Th9 spinal transection model in adult SD rat represents a reliable experimental platform to be used in studying the pathophysiology of chronic spinal injury-induced spasticity. In addition a consistent anti-spastic effect measured after treatment with clinically effective anti-spastic agents indicate that this model can effectively be used in screening new anti-spasticity compounds or procedures aimed at modulating chronic spinal trauma-associated muscle spasticity.

Indexed as

AnimalsDisease Models, AnimalElectromyographyFemaleHindlimbLumbosacral RegionMaleMuscle, SkeletalMuscle SpasticityRats, Sprague-DawleyReflex, AbnormalSpinal CordSpinal Cord InjuriesThoracic VertebraeTouch Perception

Identifiers

PMID26713446
PMCPMC4705098
OpenAlexW2214311459

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.