Evidence map›Paper›PMID 40233602›Full record

ArticleAutonomic neuroscience : basic & clinical2025

Novel role for purinergic 2× subtype 4 (P2X4) receptors in the exercise pressor reflex and mechanoreflex: Effect of heart failure.

Alec L E Butenas, Ashley M Baranczuk, Raimi J Carroll, Shannon K Parr, Carl J Ade, K Sue Hageman, Timothy I Musch, Steven W Copp

Abstract read
In one paragraph

Article in Autonomic neuroscience : basic & clinical, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Alec L E ButenasDepartment of Kinesiology, Kansas State University, Manhattan, KS, United States of America.
Ashley M BaranczukDepartment of Kinesiology, Kansas State University, Manhattan, KS, United States of America.
Raimi J CarrollDepartment of Kinesiology, Kansas State University, Manhattan, KS, United States of America.
Shannon K ParrDepartment of Kinesiology, Kansas State University, Manhattan, KS, United States of America.
Carl J AdeDepartment of Kinesiology, Kansas State University, Manhattan, KS, United States of America.
K Sue HagemanDepartment of Anatomy and Physiology, Kansas State University, Manhattan, KS, United States of America.
Timothy I MuschDepartment of Kinesiology, Kansas State University, Manhattan, KS, United States of America; Department of Anatomy and Physiology, Kansas State University, Manhattan, KS, United States of America.
Steven W CoppDepartment of Kinesiology, Kansas State University, Manhattan, KS, United States of America. Electronic address: scopp@ksu.edu.

Funding

Signaling pathways regulating mechanoreflex sensitization in cardiovascular diseaseR01HL161160 · NHLBI · KANSAS STATE UNIVERSITY · PI COPP, STEVEN W · 2022 to 2025
$2.1M
Exercise Pressor Reflex Dysfunction in Heart Failure: Mechanisms and TreatmentR01HL142877 · NHLBI · KANSAS STATE UNIVERSITY · PI COPP, STEVEN W · 2018 to 2021
$1.2M
NHLBI NIH HHS R01 HL142877NHLBI NIH HHS R01 HL161160
6 · The paper itself

Abstract

We investigated the role played by ATP-sensitive purinergic 2 × 4 (P2X4) receptors on the sensory endings of thin fibre muscle afferents in exercise pressor reflex and mechanoreflex activation in healthy/SHAM rats and rats with heart failure with reduced ejection fraction (HF-rEF). We hypothesized that infusion of the P2X4 receptor antagonist 5-BDBD (8 μg) into the hindlimb arterial supply would reduce the mean arterial pressure (MAP) and renal sympathetic nerve activity (RSNA) responses to 30s of electrically-induced hindlimb skeletal muscle contraction (model of exercise pressor reflex activation) and 30s of hindlimb skeletal muscle stretch (model of mechanoreflex activation) in decerebrate, unanesthetized HF-rEF rats but not SHAM rats. Ejection fraction was significantly lower in HF-rEF (46 ± 3 %) compared to SHAM (83 ± 2 %; P < 0.001) rats. In SHAM rats, P2X4 receptor blockade had no effect on the pressor response to hindlimb muscle contraction (n = 8) or the pressor and RSNA response to muscle stretch (n = 4). However, in SHAM rats we found that P2X4 receptor blockade significantly reduced the RSNA response to muscle contraction. In HF-rEF rats, P2X4 receptor blockade reduced the pressor and RSNA response to hindlimb muscle contraction (n = 7) as well as the pressor, but not the RNSA, response to hindlimb muscle stretch (n = 8). Collectively, the data suggest that P2X4 receptors on thin fibre muscle afferent sensory endings play a role in the evoking the exercise pressor reflex in healthy subjects that is limited to RSNA, and that in HF-rEF this expands to a significant role in mechanoreflex and exercise pressor reflex-mediated blood pressure control.

Indexed as

Heart FailurePhysical Conditioning, AnimalReceptors, Purinergic P2X4ReflexAnimalsBlood PressureDisease Models, AnimalHindlimbKidneyMaleMuscle ContractionMuscle, SkeletalPurinergic P2X Receptor AntagonistsRatsRats, Sprague-DawleySympathetic Nervous SystemPurinergic P2X Receptor AntagonistsReceptors, Purinergic P2X4Exercise pressor reflexHeart failure reduced ejection fractionMuscle afferentsP2X4

Identifiers

PMID40233602
PMCPMC12229766

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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.