Evidence map›Paper›PMID 29572431›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2018

A Gain-of-Function Mutation in the α9 Nicotinic Acetylcholine Receptor Alters Medial Olivocochlear Efferent Short-Term Synaptic Plasticity.

Carolina Wedemeyer, Lucas G Vattino, Marcelo J Moglie, Jimena Ballestero, Stéphane F Maison, Mariano N Di Guilmi, Julian Taranda, M Charles Liberman, Paul A Fuchs, Eleonora Katz and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.8field-weighted citation impact, top 19% 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

18 citing papers in PubMed, 24 citations in OpenAlex.

  1. Drug Discovery Targeting Nicotinic Acetylcholine Receptors for Hearing Loss.International journal of molecular sciences · 2026
    Review
  2. Article
  3. Medial Olivocochlear Efferent Modulation of Cochlear Micromechanics Requires P2X4 Receptor in Outer Hair Cells.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  4. Review
  5. Genetic tools for studying cochlear inhibition.Frontiers in cellular neuroscience · 2024
    Review
  6. Engineering olivocochlear inhibition to reduce acoustic trauma.Molecular therapy. Methods & clinical development · 2023
    Article
  7. The role of GABAFrontiers in endocrinology · 2023
    Review
  8. Review
  9. Article
  10. Purinergic Signaling Controls Spontaneous Activity in the Auditory System throughout Early Development.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  11. Article
  12. Functional Postnatal Maturation of the Medial Olivocochlear Efferent-Outer Hair Cell Synapse.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  13. Effects of Efferent Activity on Hair Bundle Mechanics.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  14. Strengthening of the Efferent Olivocochlear System Leads to Synaptic Dysfunction and Tonotopy Disruption of a Central Auditory Nucleus.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  15. Developmental Synaptic Changes at the Transient Olivocochlear-Inner Hair Cell Synapse.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  16. Enhancement of the Medial Olivocochlear System Prevents Hidden Hearing Loss.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  17. Article
  18. 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

11 authors at 3 institutions in 2 countries.

Carolina WedemeyerInstituto de Investigaciones en Ingeniería Genética y Biología Molecular, "Dr. Héctor N. Torres", Consejo Nacional de Investigaciones Científicas y Técnicas, 1428 Ciudad Autónoma de Buenos Aires, Argentina.ORCID 0000-0003-1757-5778
Lucas G VattinoInstituto de Investigaciones en Ingeniería Genética y Biología Molecular, "Dr. Héctor N. Torres", Consejo Nacional de Investigaciones Científicas y Técnicas, 1428 Ciudad Autónoma de Buenos Aires, Argentina.ORCID 0000-0001-6340-844X
Marcelo J MoglieInstituto de Investigaciones en Ingeniería Genética y Biología Molecular, "Dr. Héctor N. Torres", Consejo Nacional de Investigaciones Científicas y Técnicas, 1428 Ciudad Autónoma de Buenos Aires, Argentina.ORCID 0000-0002-8841-2389
Jimena BallesteroInstituto de Investigaciones en Ingeniería Genética y Biología Molecular, "Dr. Héctor N. Torres", Consejo Nacional de Investigaciones Científicas y Técnicas, 1428 Ciudad Autónoma de Buenos Aires, Argentina.
Stéphane F MaisonDepartment of Otolaryngology, Harvard Medical School, Eaton-Peabody Laboratories, Massachusetts Eye and Ear Infirmary, Harvard Program in Speech and Hearing Bioscience and Technology, Boston, Massachusetts 02114.ORCID 0000-0003-2813-6439
Mariano N Di GuilmiInstituto de Investigaciones en Ingeniería Genética y Biología Molecular, "Dr. Héctor N. Torres", Consejo Nacional de Investigaciones Científicas y Técnicas, 1428 Ciudad Autónoma de Buenos Aires, Argentina.ORCID 0000-0002-3918-296X
Julian TarandaInstituto de Investigaciones en Ingeniería Genética y Biología Molecular, "Dr. Héctor N. Torres", Consejo Nacional de Investigaciones Científicas y Técnicas, 1428 Ciudad Autónoma de Buenos Aires, Argentina.
M Charles LibermanDepartment of Otolaryngology, Harvard Medical School, Eaton-Peabody Laboratories, Massachusetts Eye and Ear Infirmary, Harvard Program in Speech and Hearing Bioscience and Technology, Boston, Massachusetts 02114.ORCID 0000-0002-1973-1730
Paul A FuchsDepartment of Otolaryngology-Head and Neck Surgery, the Center for Hearing and Balance and the Center for Sensory Biology, Institute for Basic Biomedical Sciences, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.ORCID 0000-0003-4627-4114
Eleonora KatzInstituto de Investigaciones en Ingeniería Genética y Biología Molecular, "Dr. Héctor N. Torres", Consejo Nacional de Investigaciones Científicas y Técnicas, 1428 Ciudad Autónoma de Buenos Aires, Argentina.ORCID 0000-0002-5114-2899
Ana Belén ElgoyhenInstituto de Investigaciones en Ingeniería Genética y Biología Molecular, "Dr. Héctor N. Torres", Consejo Nacional de Investigaciones Científicas y Técnicas, 1428 Ciudad Autónoma de Buenos Aires, Argentina, abelgoyhen@gmail.com.ORCID 0000-0001-9487-0311
Consejo Nacional de Investigaciones Científicas y Técnicas · ARMassachusetts Eye and Ear Infirmary · USJohns Hopkins University · US

Funding

SINGLE-NEURON MARKING IN THE STUDY OF ABNORMAL COCHLEASR01DC000188 · NIDCD · MASSACHUSETTS EYE AND EAR INFIRMARY · PI Gabriel Corfas, M. Charles Liberman · 1989 to 2026
$15.1M
THE CHOLINERGIC RESPONSE OF COCHLEAR HAIR CELLSR01DC001508 · NIDCD · UNIVERSITY OF COLORADO DENVER · PI Amanda M. Lauer · 1992 to 2026
$13.2M
NIDCD NIH HHS R01 DC000188NIDCD NIH HHS R01 DC001508
6 · The paper itself

Abstract

Gain control of the auditory system operates at multiple levels. Cholinergic medial olivocochlear (MOC) fibers originate in the brainstem and make synaptic contacts at the base of the outer hair cells (OHCs), the final targets of several feedback loops from the periphery and higher-processing centers. Efferent activation inhibits OHC active amplification within the mammalian cochlea, through the activation of a calcium-permeable α9α10 ionotropic cholinergic nicotinic receptor (nAChR), functionally coupled to calcium activated SK2 potassium channels. Correct operation of this feedback requires careful matching of acoustic input with the strength of cochlear inhibition (Galambos, 1956; Wiederhold and Kiang, 1970; Gifford and Guinan, 1987), which is driven by the rate of MOC activity and short-term facilitation at the MOC-OHC synapse (Ballestero et al., 2011; Katz and Elgoyhen, 2014). The present work shows (in mice of either sex) that a mutation in the α9α10 nAChR with increased duration of channel gating (Taranda et al., 2009) greatly elongates hair cell-evoked IPSCs and Ca

Indexed as

Gain of Function MutationNeuronal PlasticityAnimalsCalcium SignalingFeedback, PhysiologicalFemaleHair Cells, AuditoryInhibitory Postsynaptic PotentialsIon Channel GatingMaleMiceNeurons, EfferentReceptors, NicotinicnAChR alpha9Receptors, Nicotiniccochleaefferent inhibitionhair cellssynaptic plasticityα9α10 nAChR

Identifiers

PMID29572431
PMCPMC5907056
OpenAlexW2789944208

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.