Evidence map›Paper›PMID 25446357›Full record

ArticleNeuroscience2015

Dynamic characteristics of otolith ocular response during counter rotation about dual yaw axes in mice.

N Shimizu, S Wood, K Kushiro, S Yanai, A Perachio, T Makishima

Open access · greenAbstract read
In one paragraph

Article in Neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 30% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Neurovestibular Compensation following Ototoxic Lesion and Labyrinthectomy.International archives of otorhinolaryngology · 2016
    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

6 authors at 3 institutions in 2 countries.

N ShimizuDepartment of Otolaryngology, University of Texas Medical Branch, 301 University Boulevard, Galveston, TX, USA. Electronic address: naokish@naramed-u.ac.jp.
S WoodDepartment of Otolaryngology, University of Texas Medical Branch, 301 University Boulevard, Galveston, TX, USA; Department of Psychology, Azusa Pacific University, Azusa, CA, USA.
K KushiroGraduate School of Human and Environmental Studies, Kyoto University, Kyoto, Japan.
S YanaiAging Neuroscience Research Team, Tokyo Metropolitan Institute of Gerontology, Tokyo, Japan.
A PerachioDepartment of Otolaryngology, University of Texas Medical Branch, 301 University Boulevard, Galveston, TX, USA.
T MakishimaDepartment of Otolaryngology, University of Texas Medical Branch, 301 University Boulevard, Galveston, TX, USA. Electronic address: tomakish@UTMB.EDU.
The University of Texas Medical Branch at Galveston · USKyoto University · JPTokyo Metropolitan Institute of Gerontology · JP

Funding

Vestibular function analysis in miceK08DC011540 · NIDCD · UNIVERSITY OF TEXAS MED BR GALVESTON · PI MAKISHIMA, TOMOKO · 2012 to 2016
$993k
NIDCD NIH HHS K08 DC011540NIDCD NIH HHS K08DC011540
6 · The paper itself

Abstract

The central vestibular system plays an important role in higher neural functions such as self-motion perception and spatial orientation. Its ability to store head angular velocity is called velocity storage mechanism (VSM), which has been thoroughly investigated across a wide range of species. However, little is known about the mouse VSM, because the mouse lacks typical ocular responses such as optokinetic after nystagmus or a dominant time constant of vestibulo-ocular reflex for which the VSM is critical. Experiments were conducted to examine the otolith-driven eye movements related to the VSM and verify its characteristics in mice. We used a novel approach to generate a similar rotating vector as a traditional off-vertical axis rotation (OVAR) but with a larger resultant gravito-inertial force (>1g) by using counter rotation centrifugation. Similar to results previously described in other animals during OVAR, two components of eye movements were induced, i.e. a sinusoidal modulatory eye movement (modulation component) on which a unidirectional nystagmus (bias component) was superimposed. Each response is considered to derive from different mechanisms; modulations arise predominantly through linear vestibulo-ocular reflex, whereas for the bias, the VSM is responsible. Data indicate that the mouse also has a well-developed vestibular system through otoliths inputs, showing its highly conserved nature across mammalian species. On the other hand, to reach a plateau state of bias, a higher frequency rotation or a larger gravito-inertial force was considered to be necessary than other larger animals. Compared with modulation, the bias had a more variable profile, suggesting an inherent complexity of higher-order neural processes in the brain. Our data provide the basis for further study of the central vestibular system in mice, however, the underlying individual variability should be taken into consideration.

Indexed as

Nystagmus, OptokineticReflex, Vestibulo-OcularRotationAnimalsCentrifugationEye Movement MeasurementsGravitationMice, Inbred C57BLOtolithic MembranePhysical Stimulationeye movementoff-vertical axis rotation (OVAR)otolithvelocity storage mechanismvestibular

Identifiers

PMID25446357
PMCPMC4284950
OpenAlexW1967289258

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.