Cargando…

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

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Markin, Sergey S., Lapshin, Roman D., Baskina, Olga S., Korotchenko, Svetlana A., Mukhina, Irina V., Ivanov, Sergei V., Semenov, Mikhail P., Beregovykh, Valerii V., Semenov, Andrey M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9409086/
https://www.ncbi.nlm.nih.gov/pubmed/36012579
http://dx.doi.org/10.3390/ijms23169307
_version_ 1784774764431147008
author Markin, Sergey S.
Lapshin, Roman D.
Baskina, Olga S.
Korotchenko, Svetlana A.
Mukhina, Irina V.
Ivanov, Sergei V.
Semenov, Mikhail P.
Beregovykh, Valerii V.
Semenov, Andrey M.
author_facet Markin, Sergey S.
Lapshin, Roman D.
Baskina, Olga S.
Korotchenko, Svetlana A.
Mukhina, Irina V.
Ivanov, Sergei V.
Semenov, Mikhail P.
Beregovykh, Valerii V.
Semenov, Andrey M.
author_sort Markin, Sergey S.
collection PubMed
description 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).
format Online
Article
Text
id pubmed-9409086
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-94090862022-08-26 Nebulized Non-Immunogenic Staphylokinase in the Mice Acute Lung Injury Model Markin, Sergey S. Lapshin, Roman D. Baskina, Olga S. Korotchenko, Svetlana A. Mukhina, Irina V. Ivanov, Sergei V. Semenov, Mikhail P. Beregovykh, Valerii V. Semenov, Andrey M. Int J Mol Sci Article 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). MDPI 2022-08-18 /pmc/articles/PMC9409086/ /pubmed/36012579 http://dx.doi.org/10.3390/ijms23169307 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Markin, Sergey S.
Lapshin, Roman D.
Baskina, Olga S.
Korotchenko, Svetlana A.
Mukhina, Irina V.
Ivanov, Sergei V.
Semenov, Mikhail P.
Beregovykh, Valerii V.
Semenov, Andrey M.
Nebulized Non-Immunogenic Staphylokinase in the Mice Acute Lung Injury Model
title Nebulized Non-Immunogenic Staphylokinase in the Mice Acute Lung Injury Model
title_full Nebulized Non-Immunogenic Staphylokinase in the Mice Acute Lung Injury Model
title_fullStr Nebulized Non-Immunogenic Staphylokinase in the Mice Acute Lung Injury Model
title_full_unstemmed Nebulized Non-Immunogenic Staphylokinase in the Mice Acute Lung Injury Model
title_short Nebulized Non-Immunogenic Staphylokinase in the Mice Acute Lung Injury Model
title_sort nebulized non-immunogenic staphylokinase in the mice acute lung injury model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9409086/
https://www.ncbi.nlm.nih.gov/pubmed/36012579
http://dx.doi.org/10.3390/ijms23169307
work_keys_str_mv AT markinsergeys nebulizednonimmunogenicstaphylokinaseinthemiceacutelunginjurymodel
AT lapshinromand nebulizednonimmunogenicstaphylokinaseinthemiceacutelunginjurymodel
AT baskinaolgas nebulizednonimmunogenicstaphylokinaseinthemiceacutelunginjurymodel
AT korotchenkosvetlanaa nebulizednonimmunogenicstaphylokinaseinthemiceacutelunginjurymodel
AT mukhinairinav nebulizednonimmunogenicstaphylokinaseinthemiceacutelunginjurymodel
AT ivanovsergeiv nebulizednonimmunogenicstaphylokinaseinthemiceacutelunginjurymodel
AT semenovmikhailp nebulizednonimmunogenicstaphylokinaseinthemiceacutelunginjurymodel
AT beregovykhvaleriiv nebulizednonimmunogenicstaphylokinaseinthemiceacutelunginjurymodel
AT semenovandreym nebulizednonimmunogenicstaphylokinaseinthemiceacutelunginjurymodel