Open AccessAnticoagulation increases alveolar hemorrhage in mice infected with influenza A
Author(s) -
Tatsumi Kohei,
Antoniak Silvio,
Subramaniam Saravanan,
Gondouin Bertrand,
Neidich Scott D.,
Beck Melinda A.,
Mickelson Jacqueline,
Monroe Dougald M.,
Bastarache Julie A.,
Mackman Nigel
Publication year - 2016
Publication title -
physiological reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.918
H-Index - 39
ISSN - 2051-817X
DOI - 10.14814/phy2.13071
Subject(s) - bronchoalveolar lavage , medicine , lung , dabigatran , influenza a virus , immunology , pneumonia , virus , warfarin , atrial fibrillation
Influenza A virus infection is a common respiratory tract infection. Alveolar hemorrhage has been reported in patients with influenza pneumonia and in mice infected with influenza A. In this study, we investigated the effect of two anticoagulants on alveolar hemorrhage after influenza A virus ( IAV ) infection of wild‐type mice. Wild‐type mice were anticoagulated with either warfarin or the direct thrombin inhibitor dabigatran etexilate and then infected with a mouse‐adapted influenza virus (A/Puerto Rico/8/34 H1N1). Alveolar hemorrhage was assessed by measuring hemoglobin levels in the bronchoalveolar lavage fluid ( BALF ). We also measured vascular permeability and viral genomes in the lung, as well as white blood cells, inflammatory mediators, and protein in BALF . Survival and body weight were monitored for 14 days after influenza A infection. In infected mice receiving either warfarin or dabigatran etexilate we observed decreased activation of coagulation in the BALF and increased alveolar hemorrhage. Warfarin but not dabigatran etexilate increased vascular permeability and mortality of influenza A‐infected mice. Anticoagulation did not affect levels of influenza A genomes, white blood cells, inflammatory mediators, or protein in the BALF . Our study indicates that systemic anticoagulation increases alveolar hemorrhage in influenza A‐infected mice.