Evidence map›Paper›PMID 30237409›Full record

ArticleScientific reports2018

Intermittent hypoxia regulates vasoactive molecules and alters insulin-signaling in vascular endothelial cells.

Pragya Sharma, Yu Dong, Virend K Somers, Timothy E Peterson, Yuebo Zhang, Shihan Wang, Guangxi Li, Prachi Singh

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.3field-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

32 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Novel Insights into the Molecular Mechanisms of Atherosclerosis.International journal of molecular sciences · 2023
    Review
  16. Review
  17. Article
  18. Article
  19. Endothelin-1 as a novel target for the prevention of metabolic dysfunction with intermittent hypoxia in male participants.American journal of physiology. Regulatory, integrative and comparative physiology · 2022
    Article
  20. 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

8 authors at 2 institutions in 2 countries.

Pragya SharmaDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, 55905, USA.
Yu DongDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, 55905, USA.
Virend K SomersDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, 55905, USA.
Timothy E PetersonDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, 55905, USA.
Yuebo ZhangDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, 55905, USA.
Shihan WangDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, 55905, USA.
Guangxi LiDepartment of Pulmonary and Critical Care Medicine, Rochester, MN, 55905, USA.
Prachi SinghDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, 55905, USA. singh.prachi@mayo.edu.
Mayo Clinic in Arizona · USGuang’anmen Hospital · CN

Funding

Disease Mechanisms in Sleep ApneaR01HL065176 · NHLBI · MAYO CLINIC ROCHESTER · PI SOMERS, VIREND K · 1999 to 2021
$5.8M
American Heart Association (American Heart Association, Inc.) 17GRNT33660138NHLBI NIH HHS R01 HL065176U.S. Department of Health & Human Services | National Institutes of Health (NIH) HL65176
6 · The paper itself

Abstract

Vascular dysfunction and insulin resistance (IR) are associated with obstructive sleep apnea (OSA), which is characterized by frequent episodes of nocturnal intermittent hypoxia (IH). While it is recognized that the balance between vasoconstrictive (endothelin-1) and vasodilatory molecules (nitric oxide, NO) determine vascular profile, molecular mechanisms contributing to vascular dysfunction and IR in OSA are not completely understood. Caveolin-1 is a membrane protein which regulates endothelial nitric oxide synthase (eNOS) activity which is responsible for NO generation and cellular insulin-signaling. Hence, we examined the effects of IH on caveolin-1, eNOS, and endothelin-1 in human coronary artery endothelial cells in the context of IR. Chronic 3-day IH exposure up-regulated caveolin-1 and endothelin-1 expression while reducing NO. Also, IH altered insulin-mediated activation of AKT but not ERK resulting in increased endothelin-1 transcription. Similarly, caveolin-1 overexpression attenuated basal and insulin-stimulated NO synthesis along with impaired insulin-dependent activation of AKT and eNOS, with no effect on insulin-stimulated ERK1/2 phosphorylation and endothelin-1 transcription. Our data suggest that IH contributes to a vasoconstrictive profile and to pathway-selective vascular IR, whereby insulin potentiates ET-1 expression. Moreover, IH may partly mediate its effects on NO and insulin-signaling via upregulating caveolin-1 expression.

Indexed as

Caveolin 1Cell HypoxiaCells, CulturedEndothelial CellsEndothelin-1HumansInsulinNitric OxideNitric Oxide Synthase Type IIIPhosphorylationProto-Oncogene Proteins c-aktSignal TransductionCaveolin 1Endothelin-1InsulinNitric OxideNitric Oxide Synthase Type IIIProto-Oncogene Proteins c-akt

Identifiers

PMID30237409
PMCPMC6148090
OpenAlexW2890201783

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.