Evidence map›Paper›PMID 27150830›Full record

ArticleJournal of applied physiology (Bethesda, Md. : 1985)2016

Perfusion-related stimuli for compensatory lung growth following pneumonectomy.

D Merrill Dane, Cuneyt Yilmaz, Dipendra Gyawali, Roshni Iyer, Priya Ravikumar, Aaron S Estrera, Connie C W Hsia

Open access · greenAbstract read
In one paragraph

Article in Journal of applied physiology (Bethesda, Md. : 1985), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.5field-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

11 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Blood flow-induced angiocrine signals promote organ growth and regeneration.BioEssays : news and reviews in molecular, cellular and developmental biology · 2025
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Erythropoietin inhalation enhances adult canine alveolar-capillary formation following pneumonectomy.American journal of physiology. Lung cellular and molecular physiology · 2019
    Article
  8. Vascular Niche in Lung Alveolar Development, Homeostasis, and Regeneration.Frontiers in bioengineering and biotechnology · 2019
    Review
  9. Article
  10. Article
  11. Review
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.

D Merrill DaneDepartment of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas; and.
Cuneyt YilmazDepartment of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas; and.
Dipendra GyawaliDepartment of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas; and.
Roshni IyerDepartment of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas; and.
Priya RavikumarDepartment of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas; and.
Aaron S EstreraDepartment of Cardiothoracic Surgery, University of Texas Southwestern Medical Center, Dallas, Texas.
Connie C W HsiaDepartment of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas; and Connie.Hsia@utsouthwestern.edu.
The University of Texas Southwestern Medical Center · US

Funding

Signals for Post-pneumonectomy Compensatory Lung GrowthR01HL040070 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI HSIA, CONNIE C. W. · 1988 to 2014
$5.3M
Nanoparticle Drug Delivery in Post-Pneumonectomy Compensatory Lung GrowthU01HL111146 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI HSIA, CONNIE C. W., NGUYEN, KYTAI TRUONG · 2012 to 2016
$3.2M
NHLBI NIH HHS R01 HL040070NHLBI NIH HHS U01 HL111146
6 · The paper itself

Abstract

Following pneumonectomy (PNX), two separate mechanical forces act on the remaining lung: parenchymal stress caused by lung expansion, and microvascular distension and shear caused by increased perfusion. We previously showed that parenchymal stress and strain explain approximately one-half of overall compensation; the remainder was presumptively attributed to perfusion-related factors. In this study, we directly tested the hypothesis that perturbation of regional pulmonary perfusion modulates post-PNX lung growth. Adult canines underwent banding of the pulmonary artery (PAB) to the left caudal (LCa) lobe, which caused a reduction in basal perfusion to LCa lobe without preventing the subsequent increase in its perfusion following right PNX while simultaneously exaggerating the post-PNX increase in perfusion to the unbanded lobes, thereby creating differential perfusion changes between banded and unbanded lobes. Control animals underwent sham pulmonary artery banding followed by right PNX. Pulmonary function, regional pulmonary perfusion, and high-resolution computed tomography of the chest were analyzed pre-PNX and 3-mo post-PNX. Terminally, the remaining lobes were fixed for detailed morphometric analysis. Results were compared with corresponding lobes in two control (Sham banding and normal unoperated) groups. PAB impaired the indices of post-PNX extravascular alveolar tissue growth by up to 50% in all remaining lobes. PAB enhanced the expected post-PNX increase in alveolar capillary formation, measured by the prevalence of double-capillary profiles, in both unbanded and banded lobes. We conclude that perfusion distribution provides major stimuli for post-PNX compensatory lung growth independent of the stimuli provided by lung expansion and parenchymal stress and strain.

Indexed as

AnimalsCapillariesDogsLungLung Volume MeasurementsMalePerfusionPneumonectomyPulmonary ArteryPulmonary Gas ExchangeRegenerationStress, MechanicalTomography, X-Ray Computedalveolar angiogenesislung resectionlung structure and functionpulmonary artery bandingpulmonary blood flow

Identifiers

PMID27150830
PMCPMC4967253
OpenAlexW2345360422

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.