Evidence map›Paper›PMID 20534825›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2010

Role of chondroitin sulfate proteoglycans in axonal conduction in Mammalian spinal cord.

Arsen S Hunanyan, Guillermo García-Alías, Valentina Alessi, Joel M Levine, James W Fawcett, Lorne M Mendell, Victor L Arvanian

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

40 citing papers in PubMed, 75 citations in OpenAlex.

  1. NG2 Glia and Cellular Crosstalk in Health and Disease: Focus on Spinal Cord Injury.Pathophysiology : the official journal of the International Society for Pathophysiology · 2026
    Review
  2. Cell surface differences within the genusJournal of bacteriology · 2025
    Review
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  17. Serotonergic transmission after spinal cord injury.Journal of neural transmission (Vienna, Austria : 1996) · 2015
    Review
  18. Article
  19. 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

7 authors at 4 institutions in 2 countries.

Arsen S HunanyanNorthport Veterans Affairs Medical Center, Northport, New York 11768, USA.
Guillermo García-Alías
Valentina Alessi
Joel M Levine
James W Fawcett
Lorne M Mendell
Victor L Arvanian
State University of New York · USUniversity of Cambridge · GBNorthport VA Medical Center · USStony Brook University · US

Funding

MECHANISMS OF PLASTICITY IN NEURONAL CONNECTIONSR01NS016996 · NINDS · STATE UNIVERSITY NEW YORK STONY BROOK · PI MENDELL, LORNE M · 1985 to 2011
$3.9M
BIOMECHANICS OF THE MIDDLE EARR01NS021998 · NINDS · OHIO STATE UNIVERSITY · PI HETHERINGTON, THOMAS E · 1988 to 1988
–
NINDS NIH HHS 5 RO1 NS16996NINDS NIH HHS R01 NS016996NINDS NIH HHS R01 NS 21998
6 · The paper itself

Abstract

Chronic unilateral hemisection (HX) of the adult rat spinal cord diminishes conduction through intact fibers in the ventrolateral funiculus (VLF) contralateral to HX. This is associated with a partial loss of myelination from fibers in the VLF (Arvanian et al., 2009). Here, we again measured conduction through the VLF using electrical stimulation while recording the resulting volley and synaptic potentials in target motoneurons. We found that intraspinal injection of chondroitinase-ABC, known to digest chondroitin sulfate proteoglycans (CSPGs), prevented the decline of axonal conduction through intact VLF fibers across from chronic T10 HX. Chondroitinase treatment was also associated with behavior suggestive of an improvement of locomotor function after chronic HX. To further study the role of CSPGs in axonal conduction, we injected three purified CSPGs, NG2 and neurocan, which increase in the vicinity of a spinal injury, and aggrecan, which decreases, into the lateral column of the uninjured cord at T10 in separate experiments. Intraspinal injection of NG2 acutely depressed axonal conduction through the injected region in a dose-dependent manner. Similar injections of saline, aggrecan, or neurocan had no significant effect. Immunofluorescence staining experiments revealed the presence of endogenous and exogenous NG2 at some nodes of Ranvier. These results identify a novel acute action of CSPGs on axonal conduction in the spinal cord and suggest that antagonism of proteoglycans reverses or prevents the decline of axonal conduction, in addition to stimulating axonal growth.

Indexed as

Action PotentialsAggrecansAnimalsAntigensAxonsChondroitin ABC LyaseChondroitin Sulfate Proteoglycan 4Chondroitin Sulfate ProteoglycansDisease Models, AnimalElectric StimulationFemaleFluorescent Antibody TechniqueFunctional LateralityInjections, SpinalMotor ActivityMotor NeuronsAggrecansAntigensChondroitin ABC LyaseChondroitin Sulfate Proteoglycan 4Chondroitin Sulfate ProteoglycansNcan protein, ratNeurocanProteoglycans

Identifiers

PMID20534825
PMCPMC3531897
OpenAlexW2066340179

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.