Evidence map›Paper›PMID 35853986›Full record

ArticleScientific reports2022

Low frequency visual stimulation enhances slow wave activity without disrupting the sleep pattern in mice.

Stephen Thankachan, Chun Yang, Ksenia V Kastanenka, Brian J Bacskai, Dmitry Gerashchenko

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. 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 47% 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, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Cortex-specific inversion of visual responses during sleep.bioRxiv : the preprint server for biology · 2026
    Article
  4. 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

5 authors at 3 institutions in 1 country.

Stephen ThankachanVeterans Affairs Boston Healthcare System, Harvard Medical School, West Roxbury, MA, 02132, USA.
Chun YangVeterans Affairs Boston Healthcare System, Harvard Medical School, West Roxbury, MA, 02132, USA.
Ksenia V KastanenkaDepartment of Neurology, MassGeneral Institute of Neurodegenerative Diseases, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA, 02129, USA.
Brian J BacskaiDepartment of Neurology, MassGeneral Institute of Neurodegenerative Diseases, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA, 02129, USA.
Dmitry GerashchenkoVeterans Affairs Boston Healthcare System, Harvard Medical School, West Roxbury, MA, 02132, USA. dmitry_gerashchenko@hms.harvard.edu.
Massachusetts General Hospital · USVA Boston Healthcare System · USHarvard University · US

Funding

Slow-wave activity as a modifier of the progression of neurodegeneration in Alzheimer's diseaseRF1AG061774 · NIA · HARVARD MEDICAL SCHOOL · PI BACSKAI, BRIAN J, GERASHCHENKO, DMITRY · 2019 to 2021
$3.7M
Elucidating circuit disruptions in Alzheimer's diseaseR01AG066171 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI KASTANENKA, KSENIA V. · 2020 to 2024
$2.9M
Novel molecular genetic tool for large-scale labeling and modulating activity of neurons associated with particular physiological processes and behaviorsR21NS106406 · NINDS · HARVARD MEDICAL SCHOOL · PI GERASHCHENKO, DMITRY · 2018 to 2019
$375k
NIA NIH HHS AG061774NIA NIH HHS R01 AG066171NIA NIH HHS RF1 AG061774NINDS NIH HHS NS106406NINDS NIH HHS R21 NS106406
6 · The paper itself

Abstract

Non-invasive stimulation technologies are emerging as potential treatment options for a range of neurodegenerative disorders. Experimental evidence suggests that stimuli-evoked changes in slow brain rhythms may mitigate or even prevent neuropathological and behavioral impairments. Slow wave activity is prevalent during sleep and can be triggered non-invasively by sensory stimulation targeting the visual system or directly via activation of neurons locally using optogenetics. Here, we developed new tools for delivering visual stimulation using light-emitting diodes in freely moving mice while awake and during sleep. We compared these tools to traditional optogenetic approaches used for local stimulation of neurons in the cerebral cortex. We then used these tools to compare the effects of low-frequency visual versus optogenetic stimulations on the slow wave activity and sleep pattern in mice. Visual stimulation effectively enhanced slow wave activity without disrupting the sleep pattern. Optogenetic stimulation of cortical GABAergic neurons increased NREM sleep. These results suggest that visual stimulation can be effective at boosting slow wave activity without having adverse effects on sleep and thus holds great potential as a non-invasive stimulation treatment strategy.

Indexed as

Sleep, Slow-WaveAnimalsElectroencephalographyMiceOptogeneticsPhotic StimulationSleepWakefulness

Identifiers

PMID35853986
PMCPMC9296645
OpenAlexW4285797180

What OpenQuestion holds

Textmetadata
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.