Evidence map›Paper›PMID 22764237›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2012

Generating synchrony from the asynchronous: compensation for cochlear traveling wave delays by the dendrites of individual brainstem neurons.

Matthew J McGinley, M Charles Liberman, Ramazan Bal, Donata Oertel

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

42 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Asymmetry in the Perception of Electrical Chirps Presented to Cochlear Implant Listeners.Journal of the Association for Research in Otolaryngology : JARO · 2024
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Mammalian octopus cells are direction selective to frequency sweeps by excitatory synaptic sequence detection.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Information Processing by Onset Neurons in the Cat Auditory Brainstem.Journal of the Association for Research in Otolaryngology : JARO · 2020
    Article
  17. Periodicity Pitch Perception.Frontiers in neuroscience · 2020
    Article
  18. Article
  19. Article
  20. 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

4 authors at 2 institutions in 1 country.

Matthew J McGinleyDepartment of Neuroscience, School of Medicine and Public Health, University of Wisconsin, Madison, Madison, Wisconsin 53706, USA. matthew.mcginley@yale.edu
M Charles Liberman
Ramazan Bal
Donata Oertel
University of Wisconsin–Madison · USMassachusetts Eye and Ear Infirmary · US

Funding

Imaging Core PlanP30DC005209 · NIDCD · MASSACHUSETTS EYE AND EAR INFIRMARY · PI ADAMS, JOE C · 2002 to 2016
$12.0M
IN VITRO STUDIES OF THE COCHLEAR NUCLEUSR01DC000176 · NIDCD · UNIVERSITY OF WISCONSIN-MADISON · PI SUGDEN, DONATA OERTEL · 1989 to 2014
$5.5M
PATCH CLAMP ANALYSIS OF OLFACTORY NEURONSF32DC000176 · NIDCD · BOSTON UNIVERSITY MEDICAL CAMPUS · PI DELAY, RONA J · 1995 to 1997
–
NIDCD NIH HHS DC00176NIDCD NIH HHS F32 DC000176NIDCD NIH HHS P30 DC005209NIDCD NIH HHS R01 DC000176
6 · The paper itself

Abstract

Broadband transient sounds, such as clicks and consonants, activate a traveling wave in the cochlea. This wave evokes firing in auditory nerve fibers that are tuned to high frequencies several milliseconds earlier than in fibers tuned to low frequencies. Despite this substantial traveling wave delay, octopus cells in the brainstem receive broadband input and respond to clicks with submillisecond temporal precision. The dendrites of octopus cells lie perpendicular to the tonotopically organized array of auditory nerve fibers, placing the earliest arriving inputs most distally and the latest arriving closest to the soma. Here, we test the hypothesis that the topographic arrangement of synaptic inputs on dendrites of octopus cells allows octopus cells to compensate the traveling wave delay. We show that in mice the full cochlear traveling wave delay is 1.6 ms. Because the dendrites of each octopus cell spread across approximately one-third of the tonotopic axis, a click evokes a soma-directed sweep of synaptic input lasting 0.5 ms in individual octopus cells. Morphologically and biophysically realistic, computational models of octopus cells show that soma-directed sweeps with durations matching in vivo measurements result in the largest and sharpest somatic EPSPs. A low input resistance and activation of a low-voltage-activated potassium conductance that are characteristic of octopus cells are important determinants of sweep sensitivity. We conclude that octopus cells have dendritic morphologies and biophysics tailored to accomplish the precise encoding of broadband transient sounds.

Indexed as

Models, NeurologicalAcoustic StimulationAnimalsAuditory PathwaysBrain WavesCochleaCochlear NerveCochlear NucleusDendritesExcitatory Postsynaptic PotentialsFemaleHumansMaleMiceMice, Inbred CBAMice, Inbred ICR

Identifiers

PMID22764237
PMCPMC3417346
OpenAlexW2061538174

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.