Evidence map›Paper›PMID 39971146›Full record

ArticleRespiratory physiology & neurobiology2025

Bulk and regional diaphragm blood flow during chemical hyperpnea in pulmonary hypertensive rats.

Kiana M Schulze, Andrew G Horn, Ramona E Weber, K Sue Hageman, Britton C Scheuermann, Carl J Ade, Bradley J Behnke, David C Poole, Timothy I Musch

Abstract read
In one paragraph

Article in Respiratory physiology & neurobiology, 2025. 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

9 authors.

Kiana M SchulzeDepartment of Kinesiology, Kansas State University, Manhattan, KS, United States. Electronic address: kiana7@ksu.edu.
Andrew G HornDepartment of Kinesiology, Kansas State University, Manhattan, KS, United States.
Ramona E WeberDepartment of Kinesiology, Kansas State University, Manhattan, KS, United States.
K Sue HagemanDepartment of Anatomy and Physiology, Kansas State University, Manhattan, KS, United States.
Britton C ScheuermannDepartment of Kinesiology, Kansas State University, Manhattan, KS, United States.
Carl J AdeDepartment of Kinesiology, Kansas State University, Manhattan, KS, United States.
Bradley J BehnkeDepartment of Kinesiology, Kansas State University, Manhattan, KS, United States.
David C PooleDepartment of Kinesiology, Kansas State University, Manhattan, KS, United States; Department of Anatomy and Physiology, Kansas State University, Manhattan, KS, United States.
Timothy I MuschDepartment of Kinesiology, Kansas State University, Manhattan, KS, United States; Department of Anatomy and Physiology, Kansas State University, Manhattan, KS, United States.

Funding

DO HEART FAILURE AND AGING POTENTIATE DIAPHRAGM VASCULAR DYSFUNCTION?R15AG078060 · NIA · KANSAS STATE UNIVERSITY · PI BEHNKE, BRAD J, POOLE, DAVID C · 2021 to 2021
$456k
Role for Nrf2 and exercise in mitigating pulmonary hypertension-induced vascular dysfunctionF31HL170643 · NHLBI · KANSAS STATE UNIVERSITY · PI SCHULZE, KIANA MARIE · 2023 to 2024
$73k
ROLE OF ANGIOTENSIN-(1-7) AND DIAPHRAGM VASCULAR FUNCTION IN HEART FAILURE AND PROLONGED MECHANICAL VENTILATIONF31HL167618 · NHLBI · KANSAS STATE UNIVERSITY · PI HORN, ANDREW · 2023 to 2024
$72k
NHLBI NIH HHS F31 HL167618NHLBI NIH HHS F31 HL170643NIA NIH HHS R15 AG078060
6 · The paper itself

Abstract

Pulmonary hypertension (PH) is a disease characterized by increased pulmonary arterial pressures, impaired gas exchange, dyspnea, and diaphragmatic dysfunction. Specifically, in PH, the diaphragm displays impaired contractility, vascular dysfunction, and blood flow redistribution toward less mechanically advantageous regions such as the ventral costal and crural diaphragm at rest and during submaximal exercise. While diaphragm blood flow is not a limitation to maximal exercise in health, whether it limits diaphragm function in PH is unknown. We hypothesized that, during chemically induced hyperpnea: 1) diaphragm blood flow will be lower in rats with PH compared with healthy controls due to vasodilatory impairments in the diaphragm vasculature, and 2) in PH, blood flow will be redistributed toward less mechanically advantageous regions of the diaphragm. Female Sprague-Dawley rats were randomized into healthy (n = 12) or monocrotaline-induced PH (n = 12) groups. Fluorescent microspheres were used to determine bulk and regional diaphragm blood flow at rest and during hypoxic-hypercapnic gas inhalation (10 % O

Indexed as

DiaphragmHypercapniaHypertension, PulmonaryRegional Blood FlowAnimalsDisease Models, AnimalFemaleMonocrotalineRatsRats, Sprague-DawleyMonocrotalineHypercapniaHypoxiaMonocrotalineOxygen transportPerfusionRespiratory muscleVascular function

Identifiers

PMID39971146
PMCPMC12068979

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.