Evidence map›Paper›PMID 22159095›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2011

Chondroitinase ABC combined with neurotrophin NT-3 secretion and NR2D expression promotes axonal plasticity and functional recovery in rats with lateral hemisection of the spinal cord.

Guillermo García-Alías, Hayk A Petrosyan, Lisa Schnell, Philip J Horner, William J Bowers, Lorne M Mendell, James W Fawcett, Victor L Arvanian

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
5.9field-weighted citation impact, top 2% 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

43 citing papers in PubMed, 101 citations in OpenAlex.

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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

8 authors at 7 institutions in 4 countries.

Guillermo García-AlíasCentre for Brain Repair, University of Cambridge, Cambridge CB2 0PY, United Kingdom.
Hayk A Petrosyan
Lisa Schnell
Philip J Horner
William J Bowers
Lorne M Mendell
James W Fawcett
Victor L Arvanian
Cambridge School · PTCenter for Neuro-Oncology · USNorthport VA Medical Center · USState University of New York · USStony Brook University · USUniversity of Rochester Medical Center · USUniversity of Zurich · CH

Funding

MECHANISMS OF PLASTICITY IN NEURONAL CONNECTIONSR01NS016996 · NINDS · STATE UNIVERSITY NEW YORK STONY BROOK · PI MENDELL, LORNE M · 1985 to 2011
$3.9M
NINDS NIH HHS 5R01 NS 16996NINDS NIH HHS R01 NS016996
6 · The paper itself

Abstract

Elevating spinal levels of neurotrophin NT-3 (NT3) while increasing expression of the NR2D subunit of the NMDA receptor using a HSV viral construct promotes formation of novel multisynaptic projections from lateral white matter (LWM) axons to motoneurons in neonates. However, this treatment is ineffective after postnatal day 10. Because chondroitinase ABC (ChABC) treatment restores plasticity in the adult CNS, we have added ChABC to this treatment and applied the combination to adult rats receiving a left lateral hemisection (Hx) at T8. All hemisected animals initially dragged the ipsilateral hindpaw and displayed abnormal gait. Rats treated with ChABC or NT3/HSV-NR2D recovered partial hindlimb locomotor function, but animals receiving combined therapy displayed the most improved body stability and interlimb coordination [Basso-Beattie-Bresnahan (BBB) locomotor scale and gait analysis]. Electrical stimulation of the left LWM at T6 did not evoke any synaptic response in ipsilateral L5 motoneurons of control hemisected animals, indicating interruption of the white matter. Only animals with the full combination treatment recovered consistent multisynaptic responses in these motoneurons indicating formation of a detour pathway around the Hx. These physiological findings were supported by the observation of increased branching of both cut and intact LWM axons into the gray matter near the injury. ChABC-treated animals displayed more sprouting than control animals and those receiving NT3/HSV-NR2D; animals receiving the combination of all three treatments showed the most sprouting. Our results indicate that therapies aimed at increasing plasticity, promoting axon growth and modulating synaptic function have synergistic effects and promote better functional recovery than if applied individually.

Indexed as

Analysis of VarianceAnimalsAxonsbeta-GalactosidaseBiotinCells, CulturedChondroitin ABC LyaseChondroitin Sulfate ProteoglycansDextransDisease Models, AnimalExcitatory Postsynaptic PotentialsFemaleFibroblastsGene Expression RegulationGreen Fluorescent ProteinsHyperalgesiabeta-GalactosidaseBiotinbiotinylated dextran amineChondroitin ABC LyaseChondroitin Sulfate ProteoglycansDextransGreen Fluorescent ProteinsNeurotrophin 3NR2D NMDA receptorReceptors, N-Methyl-D-Aspartate

Identifiers

PMID22159095
PMCPMC3758578
OpenAlexW2032972266

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.