Inhibition of Meprins Reduces Pulmonary Edema in LPS-Induced Acute Lung Damage


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Resumo

Pulmonary edema is the major factor of tissue hypoxia in acute lung injury. Disruption of cell—cell contacts and lung interstitium increases permeability of the vascular endothelium and alveolar epithelium, which leads to the development of pulmonary edema. Meprin metalloproteases cleave extracellular matrix proteins, thus aggravating pulmonary edema. Meprin inhibitor actinonin was administered to rats with LPS-induced acute lung injury. Damaged lungs looked spotted and had multiple hemorrhage focuses, protein concentration in lavage fluid was increased, and lung weight coefficient was high. Administration of meprin inhibitor actinonin considerably reduced protein content in the bronchoalvelolar lavage and lung coefficient; only solitary lung hemorrhages were seen after this treatment. Thus, inhibition of meprins potentially alleviates LPS-induced disorders in the lung tissue permeability and reduces pulmonary edema.

Sobre autores

D. Chepurnova

National Medical Research Center for Cardiology, Ministry of Health of the Russian Federation

Email: erihter@mail.ru
Rússia, Moscow

Е. Samoilova

National Medical Research Center for Cardiology, Ministry of Health of the Russian Federation

Autor responsável pela correspondência
Email: erihter@mail.ru
Rússia, Moscow

А. Verin

Vascular Biology Center and Pulmonary Division at Augusta University

Email: erihter@mail.ru
Estados Unidos da América, Augusta, GA

A. Fesenko

National Medical Research Center for Cardiology, Ministry of Health of the Russian Federation

Email: erihter@mail.ru
Rússia, Moscow

А. Anisimov

National Medical Research Center for Cardiology, Ministry of Health of the Russian Federation

Email: erihter@mail.ru
Rússia, Moscow

A. Korotaeva

National Medical Research Center for Cardiology, Ministry of Health of the Russian Federation

Email: erihter@mail.ru
Rússia, Moscow


Declaração de direitos autorais © Springer Science+Business Media, LLC, part of Springer Nature, 2019

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