Evidence map›Paper›PMID 25565973›Full record

ArticleFrontiers in neural circuits2014

Rapid development of Purkinje cell excitability, functional cerebellar circuit, and afferent sensory input to cerebellum in zebrafish.

Jui-Yi Hsieh, Brittany Ulrich, Fadi A Issa, Jijun Wan, Diane M Papazian

Abstract 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 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed.

  1. Article
  2. Critical period plasticity enables credit assignment.bioRxiv : the preprint server for biology · 2026
    Article
  3. Review
  4. Article
  5. Development, circuitry, and function of the zebrafish cerebellum.Cellular and molecular life sciences : CMLS · 2023
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Functionally distinct Purkinje cell types show temporal precision in encoding locomotion.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  12. Article
  13. Integration of Swimming-Related Synaptic Excitation and Inhibition by olig2The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  14. Modeling Neurodegenerative Spinocerebellar Ataxia Type 13 in Zebrafish Using a Purkinje Neuron Specific Tunable Coexpression System.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  15. Article
  16. Article
  17. Development of vestibular behaviors in zebrafish.Current opinion in neurobiology · 2018
    Review
  18. Review
  19. Article
  20. Review
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.

Jui-Yi HsiehDepartment of Physiology, David Geffen School of Medicine at University of California Los Angeles Los Angeles, CA, USA ; Interdepartmental Ph.D. Program in Molecular, Cellular, and Integrative Physiology, David Geffen School of Medicine at University of California Los Angeles Los Angeles, CA, USA.
Brittany UlrichDepartment of Physiology, David Geffen School of Medicine at University of California Los Angeles Los Angeles, CA, USA ; Interdepartmental Ph.D. Program in Molecular, Cellular, and Integrative Physiology, David Geffen School of Medicine at University of California Los Angeles Los Angeles, CA, USA.
Fadi A IssaDepartment of Physiology, David Geffen School of Medicine at University of California Los Angeles Los Angeles, CA, USA.
Jijun WanDepartment of Neurology, David Geffen School of Medicine at University of California Los Angeles Los Angeles, CA, USA.
Diane M PapazianDepartment of Physiology, David Geffen School of Medicine at University of California Los Angeles Los Angeles, CA, USA ; Interdepartmental Ph.D. Program in Molecular, Cellular, and Integrative Physiology, David Geffen School of Medicine at University of California Los Angeles Los Angeles, CA, USA ; Molecular Biology Institute, David Geffen School of Medicine at University of California Los Angeles Los Angeles, CA, USA.

Funding

Kv3.3 K+ Channels and Neuronal Excitability in Spinocerebellar Ataxia Type 13R01NS058500 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI PAPAZIAN, DIANE M · 2008 to 2011
$1.3M
NINDS NIH HHS R01 NS058500NINDS NIH HHS R01NS058500
6 · The paper itself

Abstract

The zebrafish has significant advantages for studying the morphological development of the brain. However, little is known about the functional development of the zebrafish brain. We used patch clamp electrophysiology in live animals to investigate the emergence of excitability in cerebellar Purkinje cells, functional maturation of the cerebellar circuit, and establishment of sensory input to the cerebellum. Purkinje cells are born at 3 days post-fertilization (dpf). By 4 dpf, Purkinje cells spontaneously fired action potentials in an irregular pattern. By 5 dpf, the frequency and regularity of tonic firing had increased significantly and most cells fired complex spikes in response to climbing fiber activation. Our data suggest that, as in mammals, Purkinje cells are initially innervated by multiple climbing fibers that are winnowed to a single input. To probe the development of functional sensory input to the cerebellum, we investigated the response of Purkinje cells to a visual stimulus consisting of a rapid change in light intensity. At 4 dpf, sudden darkness increased the rate of tonic firing, suggesting that afferent pathways carrying visual information are already active by this stage. By 5 dpf, visual stimuli also activated climbing fibers, increasing the frequency of complex spiking. Our results indicate that the electrical properties of zebrafish and mammalian Purkinje cells are highly conserved and suggest that the same ion channels, Nav1.6 and Kv3.3, underlie spontaneous pacemaking activity. Interestingly, functional development of the cerebellum is temporally correlated with the emergence of complex, visually-guided behaviors such as prey capture. Because of the rapid formation of an electrically-active cerebellum, optical transparency, and ease of genetic manipulation, the zebrafish has great potential for functionally mapping cerebellar afferent and efferent pathways and for investigating cerebellar control of motor behavior.

Indexed as

Action PotentialsAfferent PathwaysAnimalsAnimals, Genetically ModifiedCerebellumNAV1.6 Voltage-Gated Sodium ChannelOlivary NucleusPatch-Clamp TechniquesPhotic StimulationPurkinje CellsShaw Potassium ChannelsVisual PerceptionZebrafishZebrafish Proteinskcnc3a protein, zebrafishNAV1.6 Voltage-Gated Sodium ChannelShaw Potassium ChannelsZebrafish Proteinscerebellumclimbing fiberparallel fiberpatch clampPurkinje cellvisual inputzebrafish

Identifiers

PMID25565973
PMCPMC4271617

What OpenQuestion holds

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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.