Evidence map›Paper›PMID 27761109›Full record

ArticleFrontiers in systems neuroscience2016

Saccadic and Postsaccadic Disconjugacy in Zebrafish Larvae Suggests Independent Eye Movement Control.

Chien-Cheng Chen, Christopher J Bockisch, Dominik Straumann, Melody Ying-Yu Huang

Abstract read
In one paragraph

Article in Frontiers in systems neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Dog eye movements are slower than human eye movements.Journal of eye movement research · 2020
    Article
  5. ZebrafishThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  6. 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

4 authors.

Chien-Cheng ChenDepartment of Neurology, University Hospital Zurich, University of ZurichZurich, Switzerland; PhD Program in Integrative Molecular Medicine, Life Science Graduate School, University of ZurichZurich, Switzerland.
Christopher J BockischDepartment of Neurology, University Hospital Zurich, University of ZurichZurich, Switzerland; Department of Ophthalmology, University Hospital Zurich, University of ZurichZurich, Switzerland; Department of Otorhinolaryngology, University Hospital Zurich, University of ZurichZurich, Switzerland.
Dominik StraumannDepartment of Neurology, University Hospital Zurich, University of ZurichZurich, Switzerland; Zurich Center for Integrative Human Physiology (ZIHP), University of ZurichZurich, Switzerland; Neuroscience Center Zurich (ZNZ), University of Zurich and ETH ZurichZurich, Switzerland.
Melody Ying-Yu HuangDepartment of Neurology, University Hospital Zurich, University of ZurichZurich, Switzerland; Zurich Center for Integrative Human Physiology (ZIHP), University of ZurichZurich, Switzerland; Neuroscience Center Zurich (ZNZ), University of Zurich and ETH ZurichZurich, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spontaneous eye movements of zebrafish larvae in the dark consist of centrifugal saccades that move the eyes from a central to an eccentric position and postsaccadic centripetal drifts. In a previous study, we showed that the fitted single-exponential time constants of the postsaccadic drifts are longer in the temporal-to-nasal (T->N) direction than in the nasal-to-temporal (N->T) direction. In the present study, we further report that saccadic peak velocities are higher and saccadic amplitudes are larger in the N->T direction than in the T->N direction. We investigated the underlying mechanism of this ocular disconjugacy in the dark with a top-down approach. A mathematic ocular motor model, including an eye plant, a set of burst neurons and a velocity-to-position neural integrator (VPNI), was built to simulate the typical larval eye movements in the dark. The modeling parameters, such as VPNI time constants, neural impulse signals generated by the burst neurons and time constants of the eye plant, were iteratively adjusted to fit the average saccadic eye movement. These simulations suggest that four pools of burst neurons and four pools of VPNIs are needed to explain the disconjugate eye movements in our results. A premotor mechanism controls the synchronous timing of binocular saccades, but the pools of burst and integrator neurons in zebrafish larvae seem to be different (and maybe separate) for both eyes and horizontal directions, which leads to the observed ocular disconjugacies during saccades and postsaccadic drifts in the dark.

Indexed as

brainstemgaze holdinglarvaeocular motorsaccadeszebrafish

Identifiers

PMID27761109
PMCPMC5050213

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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.