Evidence map›Paper›PMID 35434745›Full record

ArticleInflammation research : official journal of the European Histamine Research Society ... [et al.]2022

A new mouse unilateral model of diffuse alveolar damage of the lung.

A S Chernov, A A Minakov, V A Kazakov, M V Rodionov, I N Rybalkin, T N Vlasik, D V Yashin, L P Saschenko, A A Kudriaeva, A A Belogurov and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. DerinatFrontiers in pharmacology · 2022
    Article
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

18 authors at 5 institutions in 2 countries.

A S ChernovShemyakin-Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Sciences, Pushchino, Russia.
A A MinakovShemyakin-Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Sciences, Pushchino, Russia.
V A KazakovShemyakin-Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Sciences, Pushchino, Russia.
M V RodionovShemyakin-Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Sciences, Pushchino, Russia.
I N RybalkinFederal State Budgetary Institution National Medical Research Center of Cardiology, Ministry of Health of the Russian Federation, Moscow, Russia.
T N VlasikFederal State Budgetary Institution National Medical Research Center of Cardiology, Ministry of Health of the Russian Federation, Moscow, Russia.
D V YashinInstitute of Gene Biology, Russian Academy of Sciences, Moscow, Russia.
L P SaschenkoInstitute of Gene Biology, Russian Academy of Sciences, Moscow, Russia.
A A KudriaevaShemyakin-Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Sciences, Pushchino, Russia.
A A BelogurovShemyakin-Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Sciences, Pushchino, Russia.
I V SmirnovShemyakin-Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Sciences, Pushchino, Russia.
S Ya Loginova48Th Central Scientific Research Institute, Ministry of Defense of the Russian Federation, Moscow, Russia.
V N Schukina48Th Central Scientific Research Institute, Ministry of Defense of the Russian Federation, Moscow, Russia.
S V Savenko48Th Central Scientific Research Institute, Ministry of Defense of the Russian Federation, Moscow, Russia.
S V Borisevich48Th Central Scientific Research Institute, Ministry of Defense of the Russian Federation, Moscow, Russia.
K A ZykovFederal State Budgetary Institution National Medical Research Center of Cardiology, Ministry of Health of the Russian Federation, Moscow, Russia. kirillaz@inbox.ru.ORCID http://orcid.org/0000-0003-3385-2632
A G GabibovShemyakin-Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Sciences, Pushchino, Russia.
G B TeleginShemyakin-Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Sciences, Pushchino, Russia.
Institute of Bioorganic Chemistry · RU27th Central Research Institute of the Ministry of Defence of the Russian Federation · RUInstitute of Gene Biology · RUNational Medical Research Center of Cardiology · RUMoscow State University of Medicine and Dentistry · RU

Funding

Ministry of Science and Higher Education of the Russian Federation 075-15-2021-1067
6 · The paper itself

Abstract

OBJECTIVE AND

designThe existing biological models of diffuse alveolar damage (DAD) in mice have many shortcomings. To offset these shortcomings, we have proposed a simple, nonsurgical, and reproducible method of unilateral total damage of the left lung in ICR mice. This model is based on the intrabronchial administration of a mixture of bacterial lipopolysaccharide (LPS) from the cell wall of S. enterica and α-galactosylceramide (inducing substances) to the left lung.

methodsUsing computer tomography of the lungs with endobronchial administration of contrast material, we have been able to perform an operative intravital verification of the targeted delivery of the inducer. The model presented is characterized by more serious and homogeneous damage of the affected lung compared to the existing models of focal pneumonia; at the same time, our model is characterized by longer animal survival since the right lung remains intact.

resultsThe model is also characterized by diffuse alveolar damage of the left lung, animal survival of 100%, abrupt increases in plasma levels of TNFa, INFg, and IL-6, and significant myocardial overload in the right heart. It can be used to assess the efficacy of innovative drugs for the treatment of DAD and ARDS as the clinical manifestations that are developed in patients infected with SARS-CoV-2. Morphological patterns of lungs in the noninfectious ("sterile") model of DAD induced by LPS simultaneously with α-galactosylceramide (presented here) and in the infectious model of DAD induced by SARS-CoV-2 have been compared.

conclusionThe DAD model we have proposed can be widely used for studying the efficacy of candidate molecules for the treatment of infectious respiratory diseases, such as viral pneumonias of different etiology, including SARS-CoV-2.

Indexed as

COVID-19Pneumonia, ViralAnimalsDisease Models, AnimalHumansLipopolysaccharidesLungMiceMice, Inbred ICRSARS-CoV-2LipopolysaccharidesAcute respiratory distress syndromeCOVID-19Diffuse alveolar damageLungMouse model

Identifiers

PMID35434745
PMCPMC9013507
OpenAlexW4223958717

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.