Evidence map›Paper›PMID 42537220›Full record

ArticleJournal of neurophysiology2026

Sympathetic long-term facilitation following acute intermittent hypoxia is similar in the diurnal rest versus active phase in vagal-intact rats.

Alec L E Butenas, Gordon S Mitchell

Abstract read
In one paragraph

Article in Journal of neurophysiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Alec L E ButenasBreathing Research and Therapeutics Center, University of Florida, Gainesville, Florida, United States.ORCID 0000-0002-2452-5018
Gordon S MitchellMcKnight Brain Institute, University of Florida, Gainesville, Florida, United States.ORCID 0000-0002-8489-1861

Funding

Microglial regulation of intermittent hypoxia induced phrenic motor plasticityR01HL149800 · NHLBI · UNIVERSITY OF FLORIDA · PI MITCHELL, GORDON S. · 2020 to 2025
$4.2M
Regulation of Intermittent Hypoxia-Induced Respiratory Motor PlasticityR01HL148030 · NHLBI · UNIVERSITY OF FLORIDA · PI MITCHELL, GORDON S. · 2019 to 2022
$2.4M
Cellular Mechanisms of Acute-Intermittent Hypercapnic-Hypoxia Induced Phrenic Motor PlasticityF32HL176048 · NHLBI · UNIVERSITY OF FLORIDA · PI BUTENAS, ALEC LLOYD EDWARD · 2024 to 2025
$149k
HHS | National Institutes of Health (NIH) F32HL176048HHS | National Institutes of Health (NIH) R01HL148030HHS | National Institutes of Health (NIH) R01HL149800HHS | NIH | Division of Loan Repayment (DLR) L30HL175814NHLBI NIH HHS F32 HL176048NHLBI NIH HHS L30 HL175814NHLBI NIH HHS R01 HL148030NHLBI NIH HHS R01 HL149800
6 · The paper itself

Abstract

Acute intermittent hypoxia (AIH) elicits long-lasting increases in phrenic and sympathetic nerve activity, effects known as phrenic (pLTF) and sympathetic long-term facilitation (sympLTF), respectively. In anesthetized, paralyzed, vagotomized, and ventilated rats, pLTF magnitude following AIH consisting of 15, 1-min isocapnic hypoxic episodes (i.e., 15x1) is greater during the mid-rest versus mid-active phase of the diurnal cycle. However, it is unknown if sympLTF exhibits similar diurnal regulation. In urethane-anesthetized, mechanically ventilated, male Sprague-Dawley rats, we hypothesized that sympLTF elicited by 15x1 AIH ([Formula: see text] 40-55 mmHg) is greater in the mid-rest than in mid-active diurnal phase. We report renal sympathetic nerve activity (RSNA) remained elevated 90 min post-AIH, with similar responses in mid-rest (

Indexed as

Circadian RhythmHypoxiaLong-Term PotentiationPhrenic NerveSympathetic Nervous SystemVagus NerveAnimalsKidneyMaleRatsRats, Sprague-DawleyVagotomyAIHneural plasticitysLTFsympathetic LTF

Identifiers

PMID42537220
PMCPMC13584407

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.