Evidence map›Paper›PMID 25253857›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2014

Postnatal expression of neurotrophic factors accessible to spiral ganglion neurons in the auditory system of adult hearing and deafened rats.

Erin M Bailey, Steven H Green

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

32 citing papers in PubMed, 44 citations in OpenAlex.

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  6. Review
  7. Anti-inflammatory Therapy Protects Spiral Ganglion Neurons After Aminoglycoside Antibiotic-Induced Hair Cell Loss.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2023
    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

2 authors at 1 institution in 1 country.

Erin M BaileyDepartments of Biology and.
Steven H GreenDepartments of Biology and Otolaryngology, University of Iowa, Iowa City, Iowa 52242 steven-green@uiowa.edu.
University of Iowa · US

Funding

Stimuli promoting the survival of spiral ganglion neuronsR01DC002961 · NIDCD · UNIVERSITY OF IOWA · PI GREEN, STEVEN H · 1996 to 2011
$3.6M
Tissue Culture CoreP30DC010362 · NIDCD · UNIVERSITY OF IOWA · PI DAILEY, MICHAEL E, FRITZSCH, BERND · 2010 to 2014
$2.0M
Reinnervation of inner hair cells following excitotoxic traumaR01DC009405 · NIDCD · UNIVERSITY OF IOWA · PI GREEN, STEVEN H · 2011 to 2015
$1.6M
Gene Expression in Rat Cochlea Following Loss of Hair CellsF31DC011680 · NIDCD · UNIVERSITY OF IOWA · PI BAILEY, ERIN · 2011 to 2013
$93k
NIDCD NIH HHS DC009405NIDCD NIH HHS F31 DC011680NIDCD NIH HHS P30 DC010362NIDCD NIH HHS R01 DC002961NIDCD NIH HHS R01 DC009405NIDCD NIH HHS R01 DC02961
6 · The paper itself

Abstract

Spiral ganglion neurons (SGNs) receive input from cochlear hair cells and project from the cochlea to the cochlear nucleus. After destruction of hair cells with aminoglycoside antibiotics or noise, SGNs gradually die. It has been assumed that SGN death is attributable to loss of neurotrophic factors (NTFs) derived from hair cells or supporting cells in the organ of Corti (OC). We used quantitative PCR (qPCR) to assay NTF expression-neurotrophin-3 (NT-3), BDNF, GDNF, neurturin, artemin, and CNTF-in the OC and cochlear nucleus at various ages from postnatal day 0 (P0) to P90 in control hearing and neonatally deafened rats. NT-3, neurturin, and CNTF were most abundant in the postnatal hearing OC; CNTF and neurturin most abundant in the cochlear nucleus. In the OC, NT-3 and CNTF showed a postnatal increase in expression approximately concomitant with hearing onset. In rats deafened by daily kanamycin injections (from P8 to P16), surviving inner hair cells were evident at P16 but absent by P19, with most postsynaptic boutons lost before P16. NT-3 and CNTF, which normally increase postnatally, had significantly reduced expression in the OC of deafened rats, although CNTF was expressed throughout the time that SGNs were dying. In contrast, neurturin expression was constant, unaffected by deafening or by age. CNTF and neurturin expression in the cochlear nucleus was unaffected by deafening or age. Thus, NTFs other than NT-3 are available to SGNs even as they are dying after deafening, apparently conflicting with the hypothesis that SGN death is attributable to lack of NTFs.

Indexed as

AnimalsCochlear NucleusDeafnessGene Expression Regulation, DevelopmentalHair Cells, AuditoryKanamycinNerve Growth FactorsOrgan SpecificityPresynaptic TerminalsRatsRats, Sprague-DawleySpiral GanglionKanamycinNerve Growth Factorscochleadeafnessneuronal survivalneurotrophic factororgan of Cortispiral ganglion

Identifiers

PMID25253857
PMCPMC4172804
OpenAlexW2086305659

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.