Evidence map›Paper›PMID 26719087›Full record

ArticleJournal of neurophysiology2016

Target-specific regulation of presynaptic release properties at auditory nerve terminals in the avian cochlear nucleus.

J Ahn, K M MacLeod

Abstract read
In one paragraph

Article in Journal of neurophysiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Single Neuron Contributions to the Auditory Brainstem EEG.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  2. Article
  3. Article
  4. Excitatory-Inhibitory Synaptic Coupling in Avian Nucleus Magnocellularis.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    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

2 authors.

J AhnDepartment of Biology, University of Maryland, College Park, Maryland;
K M MacLeodDepartment of Biology, University of Maryland, College Park, Maryland; Neuroscience and Cognitive Science Program, University of Maryland, College Park, Maryland; and Center for the Comparative and Evolutionary Biology of Hearing, University of Maryland, College Park, Maryland macleod@umd.edu.

Funding

Neural Mechanisms of sound intensity codingR01DC010000 · NIDCD · UNIV OF MARYLAND, COLLEGE PARK · PI MACLEOD, KATRINA M · 2010 to 2020
$3.3M
NIDCD NIH HHS DC-10000NIDCD NIH HHS R01 DC010000
6 · The paper itself

Abstract

Short-term synaptic plasticity (STP) acts as a time- and firing rate-dependent filter that mediates the transmission of information across synapses. In the auditory brain stem, the divergent pathways that encode acoustic timing and intensity information express differential STP. To investigate what factors determine the plasticity expressed at different terminals, we tested whether presynaptic release probability differed in the auditory nerve projections to the two divisions of the avian cochlear nucleus, nucleus angularis (NA) and nucleus magnocellularis (NM). Estimates of release probability were made with an open-channel blocker ofN-methyl-d-aspartate (NMDA) receptors. Activity-dependent blockade of NMDA receptor-mediated excitatory postsynaptic currents (EPSCs) with application of 20 μM (+)-MK801 maleate was more rapid in NM than in NA, indicating that release probability was significantly higher at terminals in NM. Paired-pulse ratio (PPR) was tightly correlated with the blockade rate at terminals in NA, suggesting that PPR was a reasonable proxy for relative release probability at these synapses. To test whether release probability was similar across convergent inputs onto NA neurons, PPRs of different nerve inputs onto the same postsynaptic NA target neuron were measured. The PPRs, as well as the plasticity during short trains, were tightly correlated across multiple inputs, further suggesting that release probability is coordinated at auditory nerve terminals in a target-specific manner. This highly specific regulation of STP in the auditory brain stem provides evidence that the synaptic dynamics are tuned to differentially transmit the auditory information in nerve activity into parallel ascending pathways.

Indexed as

ExocytosisAnimalsChick EmbryoCochlear NerveCochlear NucleusDizocilpine MaleateExcitatory Amino Acid AntagonistsExcitatory Postsynaptic PotentialsPresynaptic TerminalsReceptors, N-Methyl-D-AspartateDizocilpine MaleateExcitatory Amino Acid AntagonistsReceptors, N-Methyl-D-Aspartateangularisdepressionmagnocellularisrelease probabilityshort-term plasticity

Identifiers

PMID26719087
PMCPMC4808089

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.