Evidence map›Paper›PMID 15056699›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2004

Common sensory inputs and differential excitability of segmentally homologous reticulospinal neurons in the hindbrain.

Hisako Nakayama, Yoichi Oda

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.0field-weighted citation impact, top 29% 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

29 citing papers in PubMed, 70 citations in OpenAlex.

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  6. Removing a single neuron in a vertebrate brain forever abolishes an essential behavior.Proceedings of the National Academy of Sciences of the United States of America · 2020
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  12. Functional motifs composed of morphologically homologous neurons repeated in the hindbrain segments.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    Article
  13. Recording field potentials from zebrafish larvae during escape responses.Journal of undergraduate neuroscience education : JUNE : a publication of FUN, Faculty for Undergraduate Neuroscience · 2014
    Article
  14. Effective sensory modality activating an escape triggering neuron switches during early development in zebrafish.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2012
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  15. Review
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  18. Mapping a sensory-motor network onto a structural and functional ground plan in the hindbrain.Proceedings of the National Academy of Sciences of the United States of America · 2011
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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 at 1 institution in 1 country.

Hisako NakayamaDivision of Biophysical Engineering, Graduate School of Engineering Science, Osaka University, Toyonaka, Osaka, Japan.
Yoichi Oda
Osaka University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the hindbrain of zebrafish and goldfish, reticulospinal (RS) neurons are arranged in seven segments, with segmental homologs in adjacent segments. The Mauthner cell (M-cell) in the fourth segment (r4) is known to trigger fast escape behavior. Its serial homologs, MiD2cm in r5 and MiD3cm in r6, are predicted to contribute to this behavior, which can be evoked by head-tap stimuli. However, little is known about their input-output properties. Therefore, we studied afferent projections from the auditory posterior eighth nerve (pVIIIn) and firing properties of MiD2cm and MiD3cm for comparison with the M-cell in adult goldfish. Labeling of RS neurons and the pVIIIn afferents with fluorescent tracers showed that the pVIIIn projected to r4-r6. Tone burst and electrical stimulation of the pVIIIn evoked EPSPs in the M-cell, MiD2cm, and MiD3cm. Stepwise depolarization typically elicited a single spike at the onset in the M-cell but repetitive spiking in MiD2cm and MiD3cm. This atypical property of the M-cell was mediated by dendrotoxin-I (DTX-I)-sensitive voltage-gated potassium channels together with recurrent inhibition, because combined application of DTX-I, strychnine, and bicuculline led to continuous repetitive firing in M-cells. The M-cell but not MiD2cm or MiD3cm expressed Kv1.2, a DTX-I-sensitive potassium channel subunit. Thus, the M-cell and its segmental homologs may sense common auditory information but send different outputs to the spinal circuits to control adaptive escape behavior.

Indexed as

Potassium Channels, Voltage-GatedAcoustic StimulationAfferent PathwaysAnimalsElapid VenomsElectric StimulationEscape ReactionEvoked PotentialsExcitatory Postsynaptic PotentialsFluorescent DyesGABA AntagonistsGlycine AgentsGoldfishKv1.2 Potassium ChannelNeuronsPotassium Channelsdendrotoxin IElapid VenomsFluorescent DyesGABA AntagonistsGlycine AgentsKv1.2 Potassium ChannelPotassium ChannelsPotassium Channels, Voltage-Gated

Identifiers

PMID15056699
PMCPMC6730040
OpenAlexW2053963648

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.