Evidence map›Paper›PMID 20580130›Full record

ArticleNeurobiology of aging2011

Age-related neuronal loss in the cochlea is not delayed by synaptic modulation.

David Jin, Kevin K Ohlemiller, Debin Lei, Elizabeth Dong, Lorna Role, David K Ryugo, Jianxin Bao

Abstract readComparative Study
In one paragraph

Article in Neurobiology of aging, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.5field-weighted citation impact, top 40% 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

9 citing papers in PubMed, 19 citations in OpenAlex.

  1. Integrating pharmacogenomics into clinical trials of hearing disorders.The Journal of the Acoustical Society of America · 2022
    Article
  2. Effect of neuregulin-1 on the auditory cortex in adult C57BL/6J mice.Iranian journal of basic medical sciences · 2020
    Article
  3. Article
  4. β-Secretase BACE1 Is Required for Normal Cochlear Function.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. 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

7 authors at 3 institutions in 1 country.

David JinDepartment of Otolaryngology, Washington University, St. Louis, MO 63110, USA.
Kevin K Ohlemiller
Debin Lei
Elizabeth Dong
Lorna Role
David K Ryugo
Jianxin Bao
Washington University in St. Louis · USJohns Hopkins University · USState University of New York · US

Funding

Sensory Function CoreP30DC004665 · NIDCD · WASHINGTON UNIVERSITY · PI FADDIS, BRIAN T · 2001 to 2015
$8.0M
DEVELOPMENT OF CLINICIAN/RESEARCHERS IN ACADEMIC ENTT32DC000022 · NIDCD · WASHINGTON UNIVERSITY · PI PICCIRILLO, JAY F. · 1989 to 2022
$5.6M
STUDIES OF THE COCHLEAR NUCLEUS GRANULE CELL DOMAINR01DC004395 · NIDCD · JOHNS HOPKINS UNIVERSITY · PI RYUGO, DAVID K. · 2000 to 2010
$3.3M
DEVELOPMENT OF A DRUG THERAPY TO AMELIORATE PERMANENT HEARING LOSSR33DC010489 · NIDCD · WASHINGTON UNIVERSITY · PI BAO, JIANXIN · 2011 to 2013
$1.7M
Roles of Neurequlin-1 in Age Related Neuronal ChangesR01AG024250 · NIA · WASHINGTON UNIVERSITY · PI BAO, JIANXIN · 2004 to 2009
$1.7M
DEVELOPMENT OF A DRUG THERAPY TO AMELIORATE PERMANENT HEARING LOSSR21DC010489 · NIDCD · WASHINGTON UNIVERSITY · PI BAO, JIANXIN · 2009 to 2010
$416k
NIA NIH HHS R01 AG024250NIA NIH HHS R01AG024250NIDCD NIH HHS DC004395NIDCD NIH HHS P30 DC004665NIDCD NIH HHS P30DC004665NIDCD NIH HHS R01 DC004395NIDCD NIH HHS R21 DC010489NIDCD NIH HHS R21DC010489NIDCD NIH HHS R33 DC010489NIDCD NIH HHS T32 DC000022NIDCD NIH HHS T32DC000022-22
6 · The paper itself

Abstract

Age-related synaptic change is associated with the functional decline of the nervous system. It is unknown whether this synaptic change is the cause or the consequence of neuronal cell loss. We have addressed this question by examining mice genetically engineered to over- or underexpress neuregulin-1 (NRG1), a direct modulator of synaptic transmission. Transgenic mice overexpressing NRG1 in spiral ganglion neurons (SGNs) showed improvements in hearing thresholds, whereas NRG1 -/+ mice show a complementary worsening of thresholds. However, no significant change in age-related loss of SGNs in either NRG1 -/+ mice or mice overexpressing NRG1 was observed, while a negative association between NRG1 expression level and survival of inner hair cells during aging was observed. Subsequent studies provided evidence that modulating NRG1 levels changes synaptic transmission between SGNs and hair cells. One of the most dramatic examples of this was the reversal of lower hearing thresholds by "turning-off" NRG1 overexpression. These data demonstrate for the first time that synaptic modulation is unable to prevent age-related neuronal loss in the cochlea.

Indexed as

Acoustic StimulationAgingAnimalsCell CountCell SurvivalCochleaHearing LossMiceMice, Inbred C57BLMice, TransgenicNeuregulin-1Spiral GanglionSynapsesSynaptic TransmissionNeuregulin-1Nrg1 protein, mouse

Identifiers

PMID20580130
PMCPMC2947614
OpenAlexW2041115771

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.