Evidence map›Paper›PMID 24405281›Full record

ArticleAmerican journal of respiratory cell and molecular biology2014

Prevention of ventilator-induced lung edema by inhalation of nanoparticles releasing ruthenium red.

Samuel C Jurek, Mariko Hirano-Kobayashi, Homer Chiang, Daniel S Kohane, Benjamin D Matthews

Open access · greenAbstract read
In one paragraph

Article in American journal of respiratory cell and molecular biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 2 pooled it
2.9field-weighted citation impact, top 9% 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

24 citing papers in PubMed, 2 syntheses or guidelines pooled it, 28 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. TRP Channels as Cellular Targets of Particulate Matter.International journal of molecular sciences · 2021
    Review
  11. Nanomedicine-Based Therapeutics to Combat Acute Lung Injury.International journal of nanomedicine · 2021
    Review
  12. Article
  13. Article
  14. Nanomedicines: A Potential Treatment for Blood Disorder Diseases.Frontiers in bioengineering and biotechnology · 2019
    Review
  15. Stromal-Interacting Molecule 1 (Stim1)/Orai1 Modulates Endothelial Permeability in Ventilator-Induced Lung Injury.Medical science monitor : international medical journal of experimental and clinical research · 2018
    Article
  16. Article
  17. Article
  18. Fluid-induced lung injury-role of TRPV4 channels.Pflugers Archiv : European journal of physiology · 2017
    Article
  19. Review
  20. 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

5 authors at 2 institutions in 1 country.

Samuel C Jurek1 Department of Medicine.
Mariko Hirano-Kobayashi
Homer Chiang
Daniel S Kohane
Benjamin D Matthews
Center for Vascular Biology Research · USBoston Children's Hospital · US

Funding

Prolonged Duration Local AnesthesiaR01GM073626 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI KOHANE, DANIEL S · 2006 to 2018
$4.7M
NIGMS NIH HHS R01 GM073626
6 · The paper itself

Abstract

The acute respiratory distress syndrome (ARDS), a devastating lung disease that has no cure, is exacerbated by life-supportive mechanical ventilation that worsens lung edema and inflammation through the syndrome of ventilator-induced lung injury. Recently, the membrane ion channel transient receptor potential vanilloid 4 (TRPV4) on alveolar macrophages was shown to mediate murine lung vascular permeability induced by high-pressure mechanical ventilation. The objective of this study was to determine whether inhalation of nanoparticles (NPs) containing the TRPV4 inhibitor ruthenium red (RR) prevents ventilator-induced lung edema in mice. Poly-lactic-co-glycolic acid NPs containing RR were evaluated in vitro for their ability to block TRPV4-mediated calcium signaling in alveolar macrophages and capillary endothelial cells. Lungs from adult C57BL6 mice treated with nebulized NPs were then used in ex vivo ventilation perfusion experiments to assess the ability of the NPs to prevent high-pressure mechanical ventilation-induced lung edema. Poly-lactic-co-glycolic acid NPs (300 nm) released RR for 150 hours in vitro, and blocked TRPV4-mediated calcium signaling in cells up to 7 days after phagocytosis. Inhaled NPs deposited in alveoli of spontaneously breathing mice were rapidly phagocytosed by alveolar macrophages, and blocked increased vascular permeability from high-pressure mechanical ventilation for 72 hours in ex vivo ventilation perfusion experiments. These data offer proof of principle that inhalation of NPs containing a TRPV4 inhibitor prevents ventilator damage for several days, and imply that this novel drug delivery strategy could be used to target alveolar macrophages in patients at risk of ventilator-induced lung injury before initiating mechanical ventilation.

Indexed as

Administration, InhalationAnimalsCalciumCalcium SignalingMacrophages, AlveolarMaleMiceMice, Inbred C57BLNanoparticlesPermeabilityPulmonary AlveoliPulmonary EdemaRespirationRespiration, ArtificialRuthenium RedTRPV Cation ChannelsCalciumRuthenium RedTrpv4 protein, mouseTRPV Cation Channels

Identifiers

PMID24405281
PMCPMC4068911
OpenAlexW2154483538

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.