Evidence map›Paper›PMID 38629828›Full record

ArticleeLife2024

Plastic vasomotion entrainment.

Daichi Sasaki, Ken Imai, Yoko Ikoma, Ko Matsui

Open access · goldAbstract read
In one paragraph

Article in eLife, 2024. 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
1.1field-weighted citation impact, top 27% 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

6 citing papers in PubMed, 4 citations in OpenAlex.

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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

4 authors at 1 institution in 2 countries.

Daichi SasakiSuper-network Brain Physiology, Graduate School of Life Sciences, Tohoku University, Sendai, Japan.
Ken ImaiSuper-network Brain Physiology, Graduate School of Life Sciences, Tohoku University, Sendai, Japan.
Yoko IkomaSuper-network Brain Physiology, Graduate School of Life Sciences, Tohoku University, Sendai, Japan.
Ko MatsuiSuper-network Brain Physiology, Graduate School of Life Sciences, Tohoku University, Sendai, Japan.ORCID https://orcid.org/0000-0003-1068-9705
Tohoku University · JP

Funding

Japan Society for the Promotion of Science 18H05110Japan Society for the Promotion of Science 19H03338Japan Society for the Promotion of Science 20H05046Japan Society for the Promotion of Science 20H05896Japan Society for the Promotion of Science 22H02713Japan Society for the Promotion of Science 22K15218Japan Society for the Promotion of Science 22KJ0262Japan Society for the Promotion of Science 23H04659
6 · The paper itself

Abstract

The presence of global synchronization of vasomotion induced by oscillating visual stimuli was identified in the mouse brain. Endogenous autofluorescence was used and the vessel 'shadow' was quantified to evaluate the magnitude of the frequency-locked vasomotion. This method allows vasomotion to be easily quantified in non-transgenic wild-type mice using either the wide-field macro-zoom microscopy or the deep-brain fiber photometry methods. Vertical stripes horizontally oscillating at a low temporal frequency (0.25 Hz) were presented to the awake mouse, and oscillatory vasomotion locked to the temporal frequency of the visual stimulation was induced not only in the primary visual cortex but across a wide surface area of the cortex and the cerebellum. The visually induced vasomotion adapted to a wide range of stimulation parameters. Repeated trials of the visual stimulus presentations resulted in the plastic entrainment of vasomotion. Horizontally oscillating visual stimulus is known to induce horizontal optokinetic response (HOKR). The amplitude of the eye movement is known to increase with repeated training sessions, and the flocculus region of the cerebellum is known to be essential for this learning to occur. Here, we show a strong correlation between the average HOKR performance gain and the vasomotion entrainment magnitude in the cerebellar flocculus. Therefore, the plasticity of vasomotion and neuronal circuits appeared to occur in parallel. Efficient energy delivery by the entrained vasomotion may contribute to meeting the energy demand for increased coordinated neuronal activity and the subsequent neuronal circuit reorganization.

Indexed as

BrainCerebellumAnimalsLearningMiceNeuronsNystagmus, OptokineticPhotic Stimulationbrainhorizontal optokinetic responsehyperemiamotor learningmouseneurosciencevasomotionvisual stimulation

Identifiers

PMID38629828
PMCPMC11023696
OpenAlexW4391604470

What OpenQuestion holds

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LicenceCC BY
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.