Evidence map›Paper›PMID 36457269›Full record

ArticleJournal of cellular and molecular medicine2022

Upregulation of IL-8, osteonectin, and myonectin mRNAs by intermittent hypoxia via OCT1- and NRF2-mediated mechanisms in skeletal muscle cells.

Shin Takasawa, Ryogo Shobatake, Asako Itaya-Hironaka, Mai Makino, Tomoko Uchiyama, Sumiyo Sakuramoto-Tsuchida, Yoshinori Takeda, Hiroyo Ota, Akiyo Yamauchi

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 11% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. The Impact of Intermittent Hypoxia on Metabolism and Cognition.International journal of molecular sciences · 2022
    Review
  10. Review
  11. Review
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

9 authors at 2 institutions in 1 country.

Shin TakasawaDepartment of Biochemistry, Nara Medical University, Nara, Japan.ORCID 0000-0002-4066-0199
Ryogo ShobatakeDepartment of Biochemistry, Nara Medical University, Nara, Japan.
Asako Itaya-HironakaDepartment of Biochemistry, Nara Medical University, Nara, Japan.
Mai MakinoDepartment of Biochemistry, Nara Medical University, Nara, Japan.
Tomoko UchiyamaDepartment of Biochemistry, Nara Medical University, Nara, Japan.
Sumiyo Sakuramoto-TsuchidaDepartment of Biochemistry, Nara Medical University, Nara, Japan.
Yoshinori TakedaDepartment of Biochemistry, Nara Medical University, Nara, Japan.
Hiroyo OtaDepartment of Biochemistry, Nara Medical University, Nara, Japan.
Akiyo YamauchiDepartment of Biochemistry, Nara Medical University, Nara, Japan.
Nara Medical University Hospital · JPNara City Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sleep apnoea syndrome is characterized by recurrent episodes of oxygen desaturation and reoxygenation (intermittent hypoxia [IH]) and is a risk factor for insulin resistance/Type 2 diabetes. The induction of insulin resistance in skeletal muscle is a key phenomenon to develop diabetes. However, the mechanisms linking IH stress and insulin resistance remain elusive. We exposed human RD and mouse C2C12 muscle cells to normoxia or IH and measured their mRNA levels by real-time RT-PCR. We found that IH significantly increased the mRNA and protein levels of muscle-derived insulin resistance-factors (myokines) such as IL-8, osteonectin (ON), and myonectin (MN) in muscle cells. We further analysed the IH-induced expression mechanisms of IL-8, ON, and MN genes in muscle cells. Deletion analyses of the human myokine promoter(s) revealed that the regions -152 to -151 in IL-8, -105 to -99 in ON, and - 3741 to -3738 in MN promoters were responsible for the activation by IH in RD cells. The promoters contain consensus transcription factor binding sequences for OCT1 in IL-8 and MN promoters, and for NRF2 in ON promoter, respectively. The introduction of siRNA for OCT1 abolished the IH-induced expression(s) of IL-8 and MN and siRNA for NRF2 abolished the IH-induced expression of ON.

Indexed as

Diabetes Mellitus, Type 2Insulin ResistanceAnimalsCollagenCytokinesHumansHypoxiaInterleukin-8MiceMuscle Fibers, SkeletalMuscle ProteinsNF-E2-Related Factor 2Octamer Transcription Factor-1OsteonectinRNA, MessengerRNA, Small InterferingC1QTNF5 protein, humanCollagenCytokinesErfe protein, mouseInterleukin-8Muscle ProteinsNF-E2-Related Factor 2Octamer Transcription Factor-1OsteonectinPOU2F1 protein, humanPou2f1 protein, mouseRNA, MessengerRNA, Small Interferingintermittent hypoxia, myokine(s)NRF2OCT1sleep apnoea syndrome

Identifiers

PMID36457269
PMCPMC9753449
OpenAlexW4310603654

What OpenQuestion holds

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LicenceCC BY
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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.