Evidence map›Paper›PMID 24909382›Full record

ArticleJournal of molecular neuroscience : MN2014

Molecular neuroimaging of post-injury plasticity.

Yan Jouroukhin, Bareng A S Nonyane, Assaf A Gilad, Galit Pelled

Open access · greenAbstract read
In one paragraph

Article in Journal of molecular neuroscience : MN, 2014. 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
0.6field-weighted citation impact, top 27% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Cortical Reorganization after Limb Loss: Bridging the Gap between Basic Science and Clinical Recovery.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Review
  2. Article
  3. Article
  4. Article
  5. New approaches for the neuroimaging of gene expression.Frontiers in integrative neuroscience · 2015
    Article
  6. Article
  7. 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

4 authors at 3 institutions in 1 country.

Yan JouroukhinF.M. Kirby Research Center for Functional Brain Imaging, Kennedy Krieger Institute, Baltimore, MD, 21205, USA.
Bareng A S Nonyane
Assaf A Gilad
Galit Pelled
Johns Hopkins University · USJohns Hopkins Medicine · USKennedy Krieger Institute · US

Funding

The Role of the Transcallosal Pathway in Neuroplasticity Following Nerve InjuryR01NS072171 · NINDS · MICHIGAN STATE UNIVERSITY · PI PELLED, GALIT · 2010 to 2019
$3.5M
Adaptive control of epileptic seizures using a genetically encoded sensorR01NS079288 · NINDS · HUGO W. MOSER RES INST KENNEDY KRIEGER · PI GILAD, ASSAF A, PELLED, GALIT · 2012 to 2015
$1.4M
NINDS NIH HHS R01 NS072171NINDS NIH HHS R01NS072171NINDS NIH HHS R01 NS079288NINDS NIH HHS R01NS079288
6 · The paper itself

Abstract

Nerve injury induces long-term changes in neuronal activity in the primary somatosensory cortex (S1), which has often been implicated as the origin of sensory dysfunction. However, the cellular mechanisms underlying this phenomenon remain unclear. C-fos is an immediate early gene, which has been shown to play an instrumental role in plasticity. By developing a new platform to image real-time changes in gene expression in vivo, we investigated whether injury modulates the levels of c-fos in layer V of S1, since previous studies have suggested that these neurons are particularly susceptible to injury. The yellow fluorescent protein, ZsYellow1, under the regulation of the c-fos promoter, was expressed throughout the rat brain. A fiber-based confocal microscope that enabled deep brain imaging was utilized, and local field potentials were collected simultaneously. In the weeks following limb denervation in adult rats (n=10), sensory stimulation of the intact limb induced significant increases in c-fos gene expression in cells located in S1, both contralateral (affected, 27.6±3 cells) and ipsilateral (8.6±3 cells) to the injury, compared to controls (n=10, 13.4±3 and 1.0±1, respectively, p value<0.05). Thus, we demonstrated that injury activates cellular mechanisms that are involved in reshaping neuronal connections, and this may translate to neurorehabilitative potential.

Indexed as

Neuronal PlasticityAction PotentialsAnimalsCell Line, TumorExtremitiesHumansNeuronsPeripheral Nerve InjuriesProto-Oncogene Proteins c-fosRatsRats, Sprague-DawleySomatosensory CortexProto-Oncogene Proteins c-fos

Identifiers

PMID24909382
PMCPMC4257867
OpenAlexW2003445579

What OpenQuestion holds

Textmetadata
LicenceTDM
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.