Evidence map›Paper›PMID 36824025›Full record

ArticleJournal of cellular and molecular medicine2023

Intermittent hypoxia treatments cause cellular priming in human microglia.

Martina De Felice, Lorenzo Germelli, Rebecca Piccarducci, Eleonora Da Pozzo, Chiara Giacomelli, Anna Baccaglini-Frank, Claudia Martini

Open access · goldFull text read
In one paragraph

Article in Journal of cellular and molecular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
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  13. Microglia and Sleep Disorders.Advances in neurobiology · 2024
    Review
  14. Intermittent hypoxia treatments cause cellular priming in human microglia.Journal of cellular and molecular medicine · 2023
    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

7 authors at 1 institution in 1 country.

Martina De FeliceDepartment of Pharmacy, University of Pisa, Pisa, Italy.
Lorenzo GermelliDepartment of Pharmacy, University of Pisa, Pisa, Italy.
Rebecca PiccarducciDepartment of Pharmacy, University of Pisa, Pisa, Italy.
Eleonora Da PozzoDepartment of Pharmacy, University of Pisa, Pisa, Italy.ORCID 0000-0003-4762-8949
Chiara GiacomelliDepartment of Pharmacy, University of Pisa, Pisa, Italy.
Anna Baccaglini-FrankDepartment of Mathematics, University of Pisa, Pisa, Italy.
Claudia MartiniDepartment of Pharmacy, University of Pisa, Pisa, Italy.
University of Pisa · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Obstructive sleep apnoea syndrome (OSAS) is a sleep-disordered breathing characterized by nocturnal collapses of the upper airway resulting in cycles of blood oxygen partial pressure oscillations, which lead to tissue and cell damage due to intermittent hypoxia (IH) episodes. Since OSAS-derived IH may lead to cognitive impairment through not fully cleared mechanisms, herein we developed a new in vitro model mimicking IH conditions to shed light on its molecular effects on microglial cells, with particular attention to the inflammatory response. The in vitro model was set-up and validated by measuring the hypoxic state, HIF-1α levels, oxidative stress by ROS production and mitochondrial activity by MTS assay. Then, the mRNA and protein levels of certain inflammatory markers (NF-κB and interleukin 6 (IL-6)) after different IH treatment protocols were investigated. The IH treatments followed by a normoxic period were not able to produce a high inflammatory state in human microglial cells. Nevertheless, microglia appeared to be in a state characterized by increased expression of NF-κB and markers related to a primed phenotype. The microglia exposed to IH cycles and stimulated with exogenous IL-1β resulted in an exaggerated inflammatory response with increased NF-κB and IL-6 expression, suggesting a role for primed microglia in OSAS-driven neuroinflammation.

Indexed as

MicrogliaSleep Apnea, ObstructiveHumansHypoxiaInterleukin-6NF-kappa BInterleukin-6NF-kappa BCD86HIF-1αHLA-DRαIL-6intermittent hypoxiamicroglial primingmild cognitive impairmentneuroinflammationNF-κBobstructive sleep apnoea syndrome

Identifiers

PMID36824025
PMCPMC10002911
OpenAlexW4321748379

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read104
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.