Evidence map›Paper›PMID 37278410›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2023

Intrapulmonary arterial contraction assay reveals region-specific deregulation of vasoreactivity to lung injuries.

Yan Bai, Guang Li, Laiming Yung, Paul B Yu, Xingbin Ai

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

6 citing papers in PubMed, 6 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

5 authors at 3 institutions in 2 countries.

Yan BaiDivision of Neonatology and Newborn Medicine, Department of Pediatrics, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, United States.ORCID 0000-0002-8393-3062
Guang LiDepartment of Critical Care Medicine, Renmin Hospital and Wuhan University, Wuhan, People's Republic of China.
Laiming YungCardiovascular Research Center, Division of Cardiovascular Medicine, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, United States.
Paul B YuCardiovascular Research Center, Division of Cardiovascular Medicine, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, United States.
Xingbin AiDivision of Neonatology and Newborn Medicine, Department of Pediatrics, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, United States.
Harvard University · USBrigham and Women's Hospital · USWuhan University · CN

Funding

Context-specific angiogenic signaling in the pulmonary vasculatureR01HL159443 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI YU, PAUL B · 2021 to 2024
$2.4M
Development of PNEC innervation and neuroplasticity after early life insultR01HL132991 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI AI, XINGBIN · 2017 to 2020
$1.8M
Cholinergic hyperinnernation in early life regulates long-term airway reactivityK08HL135443 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI BAI, YAN · 2017 to 2021
$861k
NHLBI NIH HHS K08 HL135443NHLBI NIH HHS R01 HL132991NHLBI NIH HHS R01 HL159443
6 · The paper itself

Abstract

Intrapulmonary arteries located in the proximal lung differ from those in the distal lung in size, cellular composition, and the surrounding microenvironment. However, whether these structural variations lead to region-specific regulation of vasoreactivity in homeostasis and following injury is unknown. Herein, we employ a two-step method of precision-cut lung slice (PCLS) preparation, which maintains almost intact intrapulmonary arteries, to assess contractile and relaxation responses of proximal preacinar arteries (PaAs) and distal intraacinar arteries (IaAs) in mice. We found that PaAs exhibited robust vasoconstriction in response to contractile agonists and significant nitric oxide (NO)-induced vasodilation. In comparison, IaAs were less contractile and displayed a greater relaxation response to NO. Furthermore, in a mouse model of pulmonary arterial hypertension (PAH) induced by chronic exposure to ovalbumin (OVA) allergen and hypoxia (OVA-HX), IaAs demonstrated a reduced vasocontraction despite vascular wall thickening with the emergence of new αSMA

Indexed as

Lung InjuryAnimalsHypoxiaLungMiceNitric OxideOvalbuminPulmonary ArteryVasoconstrictionVasodilationNitric OxideOvalbuminhypoxiaprecision-cut lung slicepulmonary arterial smooth muscle cellpulmonary arterypulmonary hypertension

Identifiers

PMID37278410
PMCPMC10393320
OpenAlexW4379509277

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.