Evidence map›Paper›PMID 36012579›Full record

ArticleInternational journal of molecular sciences2022

Nebulized Non-Immunogenic Staphylokinase in the Mice Acute Lung Injury Model.

Sergey S Markin, Roman D Lapshin, Olga S Baskina, Svetlana A Korotchenko, Irina V Mukhina, Sergei V Ivanov, Mikhail P Semenov, Valerii V Beregovykh, Andrey M Semenov

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. 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

9 authors at 2 institutions in 1 country.

Sergey S MarkinExperimental Drug Research and Production Zone, Institute of Biomedical Chemistry, 119121 Moscow, Russia.
Roman D LapshinCentral Research Laboratory, Privolzhsky Research Medical University, 603005 Nizhny Novgorod, Russia.
Olga S BaskinaCentral Research Laboratory, Privolzhsky Research Medical University, 603005 Nizhny Novgorod, Russia.
Svetlana A KorotchenkoCentral Research Laboratory, Privolzhsky Research Medical University, 603005 Nizhny Novgorod, Russia.
Irina V MukhinaCentral Research Laboratory, Privolzhsky Research Medical University, 603005 Nizhny Novgorod, Russia.ORCID 0000-0002-8811-0049
Sergei V IvanovLLC "SuperGene", 119270 Moscow, Russia.
Mikhail P SemenovLLC "SuperGene", 119270 Moscow, Russia.
Valerii V BeregovykhExperimental Drug Research and Production Zone, Institute of Biomedical Chemistry, 119121 Moscow, Russia.
Andrey M SemenovLLC "SuperGene", 119270 Moscow, Russia.ORCID 0000-0003-0438-9108
Privolzhsky Research Medical University · RUInstitute of Biomedical Chemistry · RU

Funding

LLC "SuperGene" not applicable
6 · The paper itself

Abstract

Acute lung injury (ALI) as a model of acute respiratory distress syndrome is characterized by inflammation, complex coagulation, and hematologic abnormalities which result in the formation of fibrin-platelet microthrombi in the pulmonary vessels with the rapid development of progressive respiratory dysfunction. We hypothesize that a nebulized fibrinolytic agent, non-immunogenic staphylokinase (nSta), may be useful for ALI therapy. First, the effect of the nebulized nSta (0.2 mg/kg, 1.0 mg/kg, or 2.0 mg/kg) on the coagulogram parameters was studied in healthy rats. ALI was induced in mice by nebulized administration of lipopolysaccharide (LPS) at a dose of 10 mg/kg. nSta (0.2 mg/kg, 0.4 mg/kg or 0.6 mg/kg) was nebulized 30 min, 24 h, and 48 h after LPS administration. The level of pro-inflammatory cytokines was determined in the blood on the 8th day after LPS and nSta administration. The assessment of lung damage was based on their weighing and microscopic analysis. Fibrin/fibrinogen deposition in the lungs was determined by immunohistochemistry. After nSta nebulization in healthy rats, the fibrinogen blood level as well as activated partial thromboplastin time and prothrombin time did not change. In the nebulized ALI model, the mice showed an increase in lung weight due to their edema and rising fibrin deposition. An imbalance of proinflammatory cytokines was also found. Forty percent of mice with ALI without nSta nebulization had died. Nebulized nSta at a dose of 0.2 mg/kg reduced the severity of ALI: a decrease in interstitial edema and inflammatory infiltration was noted. At a dose of 0.4 mg/kg of nebulized nSta, the animals showed no peribronchial edema and the bronchi had an open clear lumen. At a dose of 0.6 mg/kg of nebulized nSta, the manifestations of ALI were completely eliminated. A significant dose-dependent reduction of the fibrin-positive areas in the lungs of mice with ALI was established. Nebulized nSta had a normalizing effect on the proinflammatory cytokines in blood- interleukin (IL)-1α, IL-17A, IL-6, and granulocyte-macrophage colony-stimulating factor (GM-CSF). These data showed the effectiveness of nebulized nSta and the perspectives of its clinical usage in COVID-19 patients with acute respiratory distress syndrome (ARDS).

Indexed as

Acute Lung InjuryCOVID-19Respiratory Distress SyndromeAnimalsDisease Models, AnimalFibrinFibrinogenLipopolysaccharidesLungMetalloendopeptidasesMiceRatsauR protein, Staphylococcus aureusFibrinFibrinogenLipopolysaccharidesMetalloendopeptidasesacute lung injuryfibrimolysisfibrin-fibrinogen depositmice modelnebulized non-immunogenic staphylokinase

Identifiers

PMID36012579
PMCPMC9409086
OpenAlexW4292246806

What Socratic holds

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LicenceCC BY
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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 Socratic graph.