Recombinant Antithrombin Attenuates Acute Respiratory Distress Syndrome in Experimental Endotoxemia

Sepsis-induced endothelial acute respiratory distress syndrome is related to microvascular endothelial dysfunction caused by endothelial glycocalyx disruption. Recently, recombinant antithrombin (rAT) was reported to protect the endothelial glycocalyx from septic vasculitis; however, the underlying...

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Veröffentlicht in:The American journal of pathology 2021-09, Vol.191 (9), p.1526-1536
Hauptverfasser: Okamoto, Haruka, Muraki, Isamu, Okada, Hideshi, Tomita, Hiroyuki, Suzuki, Kodai, Takada, Chihiro, Wakayama, Yugo, Kuroda, Ayumi, Fukuda, Hirotsugu, Kawasaki, Yuki, Nishio, Ayane, Matsuo, Maho, Tamaoki, Yuto, Inagawa, Risa, Takashima, Shigeo, Taniguchi, Toshiaki, Suzuki, Akio, Suzuki, Keiko, Miyazaki, Nagisa, Kakino, Yoshinori, Yasuda, Ryu, Fukuta, Tetsuya, Kitagawa, Yuichiro, Miyake, Takahito, Doi, Tomoaki, Yoshida, Takahiro, Yoshida, Shozo, Ogura, Shinji
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Sprache:eng
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Zusammenfassung:Sepsis-induced endothelial acute respiratory distress syndrome is related to microvascular endothelial dysfunction caused by endothelial glycocalyx disruption. Recently, recombinant antithrombin (rAT) was reported to protect the endothelial glycocalyx from septic vasculitis; however, the underlying mechanism remains unknown. Here, we investigated the effect of rAT administration on vascular endothelial injury under endotoxemia. Lipopolysaccharide (LPS; 20 mg/kg) was injected intraperitoneally into 10-week-old male C57BL/6 mice, and saline or rAT was administered intraperitoneally at 3 and 24 hours after LPS administration. Subsequently, serum and/or pulmonary tissues were examined for inflammation and cell proliferation and differentiation by histologic, ultrastructural, and microarray analyses. The survival rate was significantly higher in rAT-treated mice than in control mice 48 hours after LPS injection (75% versus 20%; P 
ISSN:0002-9440
1525-2191
DOI:10.1016/j.ajpath.2021.05.015