Evidence map›Paper›PMID 24860434›Full record

ArticleFrontiers in neural circuits2014

The relative contributions of MNTB and LNTB neurons to inhibition in the medial superior olive assessed through single and paired recordings.

Michael T Roberts, Stephanie C Seeman, Nace L Golding

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neural circuits, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

31 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
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  5. Review
  6. Article
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  11. Excitatory-Inhibitory Synaptic Coupling in Avian Nucleus Magnocellularis.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  12. Review
  13. Article
  14. Article
  15. Neurotransmitters and Receptors Changes in Medial Nucleus of the Trapezoid Body (MNTB) of Early-Developmental Rats with Single-Side Deafness.Medical science monitor : international medical journal of experimental and clinical research · 2018
    Article
  16. Optogenetic Control of Neural Circuits in the Mongolian Gerbil.Frontiers in cellular neuroscience · 2018
    Article
  17. Review
  18. Article
  19. Amplitude Normalization of Dendritic EPSPs at the Soma of Binaural Coincidence Detector Neurons of the Medial Superior Olive.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    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

3 authors at 1 institution in 1 country.

Michael T RobertsDepartment of Neuroscience, Center for Learning and Memory, The University of Texas at Austin Austin, TX, USA.
Stephanie C SeemanDepartment of Neuroscience, Center for Learning and Memory, The University of Texas at Austin Austin, TX, USA.
Nace L GoldingDepartment of Neuroscience, Center for Learning and Memory, The University of Texas at Austin Austin, TX, USA.
The University of Texas at Austin · US

Funding

Dendritic Integration and Synaptic Plasticity in the MSOR01DC006877 · NIDCD · UNIVERSITY OF TEXAS AUSTIN · PI GOLDING, NACE L · 2004 to 2022
$5.9M
Synergistic in vivo and in vitro approaches in the MSOR21DC011403 · NIDCD · UNIVERSITY OF TEXAS AT AUSTIN · PI GOLDING, NACE L · 2011 to 2012
$421k
NIDCD NIH HHS R01 DC006877NIDCD NIH HHS R21 DC011403
6 · The paper itself

Abstract

The medial superior olive (MSO) senses microsecond differences in the coincidence of binaural signals, a critical cue for detecting sound location along the azimuth. An important component of this circuit is provided by inhibitory neurons of the medial and lateral nuclei of the trapezoid body (MNTB and LNTB, respectively). While MNTB neurons are fairly well described, little is known about the physiology of LNTB neurons. Using whole cell recordings from gerbil brainstem slices, we found that LNTB and MNTB neurons have similar membrane time constants and input resistances and fire brief action potentials, but only LNTB neurons fire repetitively in response to current steps. We observed that LNTB neurons receive graded excitatory and inhibitory synaptic inputs, with at least some of the latter arriving from other LNTB neurons. To address the relative timing of inhibition to the MSO from the LNTB versus the MNTB, we examined inhibitory responses to auditory nerve stimulation using a slice preparation that retains the circuitry from the auditory nerve to the MSO intact. Despite the longer physical path length of excitatory inputs driving contralateral inhibition, inhibition from both pathways arrived with similar latency and jitter. An analysis of paired whole cell recordings between MSO and MNTB neurons revealed a short and reliable delay between the action potential peak in MNTB neurons and the onset of the resulting IPSP (0.55 ± 0.01 ms, n = 4, mean ± SEM). Reconstructions of biocytin-labeled neurons showed that MNTB axons ranged from 580 to 858 μm in length (n = 4). We conclude that while both LNTB and MNTB neurons provide similarly timed inhibition to MSO neurons, the reliability of inhibition from the LNTB at higher frequencies is more constrained relative to that from the MNTB due to differences in intrinsic properties, the strength of excitatory inputs, and the presence of feedforward inhibition.

Indexed as

Action PotentialsAnimalsAuditory PathwaysCochlear NerveGerbillinaeNeural InhibitionNeuronsOlivary NucleusPonsSynapsesauditory brainstemaxoninhibitionsound localizationtiming

Identifiers

PMID24860434
PMCPMC4030206
OpenAlexW2037583784

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.