Evidence map›Paper›PMID 35861520›Full record

ArticleJournal of applied physiology (Bethesda, Md. : 1985)2022

Dose-dependent phosphorylation of endogenous Tau by intermittent hypoxia in rat brain.

Alexandria B Marciante, John Howard, Mia N Kelly, Juan Santiago Moreno, Latoya L Allen, Elisa J Gonzalez-Rothi, Gordon S Mitchell

Open access · greenAbstract read
In one paragraph

Article in Journal of applied physiology (Bethesda, Md. : 1985), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 11 citations in OpenAlex.

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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.

Alexandria B MarcianteBreathing Research and Therapeutics Center, University of Florida, Gainesville, Florida.ORCID 0000-0001-7957-6034
John HowardDepartment of Neuroscience, University of Florida, Gainesville, Florida.
Mia N KellyBreathing Research and Therapeutics Center, University of Florida, Gainesville, Florida.ORCID 0000-0002-8677-4327
Juan Santiago MorenoBreathing Research and Therapeutics Center, University of Florida, Gainesville, Florida.
Latoya L AllenBreathing Research and Therapeutics Center, University of Florida, Gainesville, Florida.
Elisa J Gonzalez-RothiBreathing Research and Therapeutics Center, University of Florida, Gainesville, Florida.ORCID 0000-0002-9833-5030
Gordon S MitchellBreathing Research and Therapeutics Center, University of Florida, Gainesville, Florida.ORCID 0000-0002-8489-1861
University of Florida · US

Funding

Functional mapping of peripheral and central circuits for airway protection and breathingOT2OD023854 · OD · UNIVERSITY OF FLORIDA · PI BOLSER, DONALD C · 2016 to 2020
$10.8M
Breathing Research and Therapeutics (BREATHE)T32HL134621 · NHLBI · UNIVERSITY OF FLORIDA · PI Gordon S. Mitchell · 2017 to 2026
$3.4M
Regulation of Intermittent Hypoxia-Induced Respiratory Motor PlasticityR01HL148030 · NHLBI · UNIVERSITY OF FLORIDA · PI MITCHELL, GORDON S. · 2019 to 2022
$2.4M
NHLBI NIH HHS R01 HL148030NHLBI NIH HHS T32 HL134621NIH HHS OT2 OD023854
6 · The paper itself

Abstract

Intermittent hypoxia, or intermittent low oxygen interspersed with normal oxygen levels, has differential effects that depend on the "dose" of hypoxic episodes (duration, severity, number per day, and number of days). Whereas "low dose" daily acute intermittent hypoxia (dAIH) elicits neuroprotection and neuroplasticity, "high dose" chronic intermittent hypoxia (CIH) similar to that experienced during sleep apnea elicits neuropathology. Sleep apnea is comorbid in >50% of patients with Alzheimer's disease-a progressive, neurodegenerative disease associated with brain amyloid and chronic Tau dysregulation (pathology). Although patients with sleep apnea present with higher Tau levels, it is unknown if sleep apnea through attendant CIH contributes to onset of Tau pathology. We hypothesized CIH characteristic of moderate sleep apnea would increase dysregulation of phosphorylated Tau (phospho-Tau) species in Sprague-Dawley rat hippocampus and prefrontal cortex. Conversely, we hypothesized that dAIH, a promising neurotherapeutic, has minimal impact on Tau phosphorylation. We report a dose-dependent intermittent hypoxia effect, with region-specific increases in

Indexed as

Alzheimer DiseaseNeurodegenerative DiseasesSleep Apnea SyndromesAnimalsBrainHumansHypoxiaOxygenPhosphorylationRatsRats, Sprague-DawleyOxygenAlzheimer’s diseaseintermittent hypoxiasleep apneaTau phosphorylation

Identifiers

PMID35861520
PMCPMC9448341
OpenAlexW4286493023

What OpenQuestion holds

Textmetadata
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.