Evidence map›Paper›PMID 23554438›Full record

ArticleJournal of neurophysiology2013

Linear summation in the barn owl's brainstem underlies responses to interaural time differences.

Paula T Kuokkanen, Go Ashida, Catherine E Carr, Hermann Wagner, Richard Kempter

Abstract read
In one paragraph

Article in Journal of neurophysiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

  1. Experience-Dependent Plasticity in Nucleus Laminaris of the Barn Owl.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  2. Somatic Integration of Incoherent Dendritic Inputs in the Gerbil Medial Superior Olive.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  3. Neural Maps of Interaural Time Difference in the American Alligator: A Stable Feature in Modern Archosaurs.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  4. Article
  5. Article
  6. Article
  7. Neural Correlates of the Binaural Masking Level Difference in Human Frequency-Following Responses.Journal of the Association for Research in Otolaryngology : JARO · 2017
    Article
  8. The Binaural Interaction Component in Barn Owl (Tyto alba) Presents few Differences to Mammalian Data.Journal of the Association for Research in Otolaryngology : JARO · 2016
    Article
  9. Article
  10. Microsecond-scale timing precision in rodent trigeminal primary afferents.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  11. Article
  12. Article
  13. A model of the medial superior olive explains spatiotemporal features of local field potentials.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    Article
  14. 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

5 authors.

Paula T KuokkanenInstitute for Theoretical Biology, Department of Biology, Humboldt-Universität zu Berlin, Berlin, Germany.
Go Ashida
Catherine E Carr
Hermann Wagner
Richard Kempter

Funding

CELLULAR MECHANISMS UNDERLYING SOUND LOCALIZATIONR01DC000436 · NIDCD · UNIV OF MARYLAND, COLLEGE PARK · PI CARR, CATHERINE EMILY · 1994 to 2017
$6.1M
CORE--IMAGINGP30DC004664 · NIDCD · UNIV OF MARYLAND, COLLEGE PARK · PI MOSS, CYNTHIA F · 2002 to 2012
$3.5M
CELLULAR MECHANISMS UNDERLYING SOUND LOCALIZATIONR29DC000436 · NIDCD · UNIVERSITY OF ROCHESTER · PI CARR, CATHERINE EMILY · 1989 to 1992
–
NIDCD NIH HHS DC-00436NIDCD NIH HHS P30 DC004664NIDCD NIH HHS P30-DC-04664NIDCD NIH HHS R01 DC000436
6 · The paper itself

Abstract

The neurophonic potential is a synchronized frequency-following extracellular field potential that can be recorded in the nucleus laminaris (NL) in the brainstem of the barn owl. Putative generators of the neurophonic are the afferent axons from the nucleus magnocellularis, synapses onto NL neurons, and spikes of NL neurons. The outputs of NL, i.e., action potentials of NL neurons, are only weakly represented in the neurophonic. Instead, the inputs to NL, i.e., afferent axons and their synaptic potentials, are the predominant origin of the neurophonic (Kuokkanen PT, Wagner H, Ashida G, Carr CE, Kempter R. J Neurophysiol 104: 2274-2290, 2010). Thus in NL the monaural inputs from the two brain sides converge and create a binaural neurophonic. If these monaural inputs contribute independently to the extracellular field, the response to binaural stimulation can be predicted from the sum of the responses to ipsi- and contralateral stimulation. We found that a linear summation model explains the dependence of the responses on interaural time difference as measured experimentally with binaural stimulation. The fit between model predictions and data was excellent, even without taking into account the nonlinear responses of NL coincidence detector neurons, although their firing rate and synchrony strongly depend on the interaural time difference. These results are consistent with the view that the afferent axons and their synaptic potentials in NL are the primary origin of the neurophonic.

Indexed as

Acoustic StimulationModels, NeurologicalAnimalsBrain StemNerve NetNeuronsStrigiformesauditory coincidence detectorextracellular field potentialneurophonicphase lockingsound localization

Identifiers

PMID23554438
PMCPMC3727037

What OpenQuestion holds

Textmetadata
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Registered trials

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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.