Evidence map›Paper›PMID 21289170›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2011

Mechanism of spontaneous activity in afferent neurons of the zebrafish lateral-line organ.

Josef G Trapani, Teresa Nicolson

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

52 citing papers in PubMed, 83 citations in OpenAlex.

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  10. Probing the role of the CFrontiers in molecular neuroscience · 2023
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  17. Unraveling the Molecular Players at the Cholinergic Efferent Synapse of the Zebrafish Lateral Line.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  18. Variability and Randomness of the Instantaneous Firing Rate.Frontiers in computational neuroscience · 2021
    Article
  19. Review
  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

2 authors at 1 institution in 1 country.

Josef G TrapaniHoward Hughes Medical Institute, Oregon Health and Science University, Portland, Oregon 97239, USA. trapanij@ohsu.edu
Teresa Nicolson
Howard Hughes Medical Institute · US

Funding

Genetic and molecular dissection of hair-cell functionR01DC006880 · NIDCD · OREGON HEALTH & SCIENCE UNIVERSITY · PI NICOLSON, TERESA A · 2004 to 2009
$2.2M
Howard Hughes Medical InstituteNIDCD NIH HHS R01 DC006880
6 · The paper itself

Abstract

Many auditory, vestibular, and lateral-line afferent neurons display spontaneous action potentials. This spontaneous spiking is thought to result from hair-cell glutamate release in the absence of stimuli. Spontaneous release at hair-cell resting potentials presumably results from Ca(V)1.3 L-type calcium channel activity. Here, using intact zebrafish larvae, we recorded robust spontaneous spiking from lateral-line afferent neurons in the absence of external stimuli. Consistent with the above assumptions, spiking was absent in mutants that lacked either Vesicular glutamate transporter 3 (Vglut3) or Ca(V)1.3. We then tested the hypothesis that spontaneous spiking resulted from sustained Ca(V)1.3 activity due to depolarizing currents that are active at rest. Mechanotransduction currents (I(MET)) provide a depolarizing influence to the resting potential. However, following block of I(MET), spontaneous spiking persisted and was characterized by longer interspike intervals and increased periods of inactivity. These results suggest that an additional depolarizing influence maintains the resting potential within the activation range of Ca(V)1.3. To test whether the hyperpolarization-activated cation current, I(h) participates in setting the resting potential, we applied I(h) antagonists. Both ZD7288 and DK-AH 269 reduced spontaneous activity. Finally, concomitant block of I(MET) and I(h) essentially abolished spontaneous activity, ostensibly by hyperpolarization outside of the activation range for Ca(V)1.3. Together, our data support a mechanism for spontaneous spiking that results from Ca(2+)-dependent neurotransmitter release at hair-cell resting potentials that are maintained within the activation range of Ca(V)1.3 channels through active I(MET) and I(h).

Indexed as

Action PotentialsAnimalsBenzazepinesCalcium Channels, L-TypeCyclic Nucleotide-Gated Cation ChannelsElectric StimulationElectrophysiologyHair Cells, AuditoryHyperpolarization-Activated Cyclic Nucleotide-Gated ChannelsLateral Line SystemMechanotransduction, CellularMembrane PotentialsNeurons, AfferentPhysical StimulationPotassium ChannelsPyrimidinesBenzazepinesCalcium Channels, L-TypeCyclic Nucleotide-Gated Cation ChannelsDK-AH 268Hyperpolarization-Activated Cyclic Nucleotide-Gated ChannelsICI D2788Potassium ChannelsPyrimidinesVesicular Glutamate Transport Proteins

Identifiers

PMID21289170
PMCPMC3065326
OpenAlexW2056415769

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.