Evidence map›Paper›PMID 26275924›Full record

ArticleBehavioural brain research2015

A behavioral and histological comparison of fluid percussion injury and controlled cortical impact injury to the rat sensorimotor cortex.

Todd C Peterson, William R Maass, Jordan R Anderson, Gail D Anderson, Michael R Hoane

Abstract readComparative Study
In one paragraph

Article in Behavioural brain research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

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  17. Teriflunomide Modulates Vascular Permeability and Microglial Activation after Experimental Traumatic Brain Injury.Molecular therapy : the journal of the American Society of Gene Therapy · 2018
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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

5 authors.

Todd C PetersonRestorative Neuroscience Laboratory, Department of Psychology, Southern Illinois University, Carbondale, IL 62901, United States. Electronic address: tcpeters@stanford.edu.
William R MaassRestorative Neuroscience Laboratory, Department of Psychology, Southern Illinois University, Carbondale, IL 62901, United States. Electronic address: bmaass@siu.edu.
Jordan R AndersonRestorative Neuroscience Laboratory, Department of Psychology, Southern Illinois University, Carbondale, IL 62901, United States. Electronic address: j.anderson822@siu.edu.
Gail D AndersonDepartment of Pharmacy, University of Washington, Seattle, WA 98195, United States. Electronic address: gaila@u.washington.edu.
Michael R HoaneRestorative Neuroscience Laboratory, Department of Psychology, Southern Illinois University, Carbondale, IL 62901, United States. Electronic address: mhoane@siu.edu.

Funding

Pharmacological Optimization of Poly-Drug Therapy in Traumatic Brain InjuryR01HD061944 · NICHD · UNIVERSITY OF WASHINGTON · PI ANDERSON, GAIL, HOANE, MICHAEL R. · 2009 to 2013
$3.1M
NICHD NIH HHS R01 HD061944NICHD NIH HHS R01HD061944-01
6 · The paper itself

Abstract

Our primary goal was to evaluate the behavioral and histological outcome of fluid percussion injury (FPI) and cortical contusion injury (CCI) to the sensorimotor cortex (SMC). The SMC has been used to evaluate neuroplasticity following CCI, but has not been extensively examined with FPI. In both the CCI and FPI models, a mechanical force of 4mm in diameter was applied over the SMC, allowing for a direct comparison to measure the relative rates of histology and recovery of function in these models. Gross behavioral deficits were found on the sensory task (tactile adhesive removal task) and multiple motor assessments (forelimb asymmetry task, forelimb placing task, and rotorod). These sensorimotor deficits occurred in the absence of cognitive deficits in the water maze. The CCI model creates focal damage with a localized injury wheras the FPI model creates a more diffuse injury causing widespread damage. Both behavioral and histological deficits ensued following both models of injury to the SMC. The neuroplastic changes and ease at which damage to this area can be measured behaviorally make this an excellent location to assess traumatic brain injury (TBI) treatments. No injury model can completely mimic the full spectrum of human TBI and any potential treatments should be validated across both focal and diffuse injury models. Both of these injury models to the SMC produce severe and enduring behavioral deficits, which are ideal for evaluating treatment options.

Indexed as

Disease Models, AnimalAnimalsAstrocytesBrain InjuriesMaleMemoryMotor ActivityMovement DisordersNerve DegenerationNeuropsychological TestsRats, Sprague-DawleyRotarod Performance TestSensation DisordersSensorimotor CortexSeverity of Illness IndexAnimal studiesAssessment toolsBehaviorCortical contusion injuryFluid percussion injurySensorimotor function

Identifiers

PMID26275924
PMCPMC4580137

What OpenQuestion holds

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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.