Evidence map›Paper›PMID 40806623›Full record

ArticleInternational journal of molecular sciences2025

Intermittent Hypoxia Induces Cognitive Dysfunction and Hippocampal Gene Expression Changes in a Mouse Model of Obstructive Sleep Apnea.

Kenta Miyo, Yuki Uchida, Ryota Nakano, Shotaro Kamijo, Masahiro Hosonuma, Yoshitaka Yamazaki, Hikaru Isobe, Fumihiro Ishikawa, Hiroshi Onimaru, Akira Yoshikawa and 4 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Observational
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

14 authors.

Kenta MiyoDepartment of Physiology, Showa Medical University School of Medicine, Tokyo 142-8555, Japan.
Yuki UchidaDepartment of Physiology, Showa Medical University School of Medicine, Tokyo 142-8555, Japan.ORCID 0000-0001-5075-9347
Ryota NakanoDepartment of Physiology, Showa Medical University Graduate School of Pharmacy, Tokyo 142-8555, Japan.ORCID 0009-0004-4898-6873
Shotaro KamijoDepartment of Physiology, Showa Medical University Graduate School of Pharmacy, Tokyo 142-8555, Japan.
Masahiro HosonumaDivision of Medical Pharmacology, Department of Pharmacology, Showa Medical University School of Medicine, Tokyo 142-8555, Japan.
Yoshitaka YamazakiDivision of Toxicology, Showa University Graduate School of Pharmacy, Tokyo 142-8555, Japan.
Hikaru IsobeDivision of Medical Pharmacology, Department of Pharmacology, Showa Medical University School of Medicine, Tokyo 142-8555, Japan.
Fumihiro IshikawaCenter for Biotechnology, Showa Medical University, Tokyo 142-8555, Japan.ORCID 0000-0003-0056-5098
Hiroshi OnimaruDepartment of Physiology, Showa Medical University School of Medicine, Tokyo 142-8555, Japan.
Akira YoshikawaDivision of Health Science Education, Showa Medical University School of Nursing and Rehabilitation Sciences, Yokohama 226-8555, Japan.ORCID 0000-0002-4424-1629
Shin-Ichi SakakibaraLaboratory for Molecular Neurobiology, Faculty of Human Sciences, Waseda University, Tokorozawa 359-1192, Japan.ORCID 0000-0001-8983-2249
Tatsunori OguchiDivision of Medical Pharmacology, Department of Pharmacology, Showa Medical University School of Medicine, Tokyo 142-8555, Japan.
Takuya YokoeDepartment of Respiratory Medicine, Showa Medical University Fujigaoka Hospital, Yokohama 227-8501, Japan.
Masahiko IzumizakiDepartment of Physiology, Showa Medical University School of Medicine, Tokyo 142-8555, Japan.ORCID 0000-0003-4377-8421

Funding

JSPS 24K14685
6 · The paper itself

Abstract

Obstructive sleep apnea syndrome (OSAS) is characterized by cycles of decreased blood oxygen saturation followed by reoxygenation due to transient apnea. Cognitive dysfunction is a complication of OSAS, but its mechanisms remain unclear. Eight-week-old C57BL/6J mice were exposed to intermittent hypoxia (IH) to model OSAS, and cognitive function and hippocampal gene expression were analyzed. Three groups were maintained for 28 days: an IH group (oxygen alternating between 10 and 21% in 2 min cycles, 8 h/day), sustained hypoxia group (SH) (10% oxygen, 8 h/day), and control group (21% oxygen). Behavioral tests and RNA sequencing (RNA-seq) analysis were performed. While Y-maze test results showed no differences, the IH group demonstrated impaired memory and learning in passive avoidance tests compared to control and SH groups. RNA-seq revealed coordinated suppression of mitochondrial function genes and oxidative stress response pathways, specifically in the IH group. RT-qPCR showed decreased

Indexed as

Cognitive DysfunctionGene Expression RegulationHippocampusHypoxiaSleep Apnea, ObstructiveAnimalsDisease Models, AnimalKelch-Like ECH-Associated Protein 1MaleMiceMice, Inbred C57BLNF-E2-Related Factor 2Oxidative StressKelch-Like ECH-Associated Protein 1NF-E2-Related Factor 2cognitive dysfunctiongene expressionhippocampusIntermittent hypoxiaobstructive sleep apnea syndrome

Identifiers

PMID40806623
PMCPMC12347648

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.