A neutrophil elastase inhibitor, sivelestat, ameliorates lung injury after hemorrhagic shock in rats

Yuichiro Toda, Toru Takahashi, Kyoichiro Maeshima, Hiroko Shimizu, Kazuyoshi Inoue, Hiroshi Morimatsu, Emiko Omori, Mamoru Takeuchi, Reiko Akagi, Kiyoshi Morita

研究成果査読

30 被引用数 (Scopus)

抄録

Hemorrhagic shock followed by resuscitation (HSR) causes neutrophil sequestration in the lung which leads to acute lung injury (ALI). Neutrophil elastase (NE) is thought to play a pivotal role in the pathogenesis of ALI. This study investigated whether sivelestat, a specific NE inhibitor, can attenuate ALI induced by HSR in rats. Male Sprague-Dawley rats were subjected to hemorrhagic shock by withdrawing blood so as to maintain a mean arterial blood pressure of 30±5 mm Hg for 60 min followed by resuscitation with the shed blood. HSR-treated animals received a bolus injection of sivelestat (10 mg/kg) intravenously at the start of resuscitation followed by continuous infusion for 60 min (10 mg/kg/h) during the resuscitation phase, or the vehicle. Lung injury was assessed by pulmonary histology, lung wet-weight to dry-weight (W/D) ratio, myeloperoxidase (MPO) activity, gene expression of tumor necrosis factor (TNF)-α and inducible nitric oxide synthase (iNOS), DNA binding activity of nuclear factor (NF)-κB, and immunohistochemical analysis of intercellular adhesion molecule (ICAM)-1. HSR treatment induced lung injury, as demonstrated by pulmonary edema with infiltration of neutrophils, the increase in lung W/D ratio, MPO activity, gene expression of TNF-α and iNOS, and DNA-binding activity of NF-κB, and enhanced expression of ICAM-1. In contrast, sivelestat treatment significantly ameliorated the HSR-induced lung injury, as judged by the marked improvement in all these indices. These results indicate that sivelestat attenuated HSR-induced lung injury at least in part through an inhibition of the inflammatory signaling pathway, in addition to the direct inhibitory effect on NE.

本文言語English
ページ(範囲)237-243
ページ数7
ジャーナルInternational journal of molecular medicine
19
2
DOI
出版ステータスPublished - 2月 2007

ASJC Scopus subject areas

  • 遺伝学

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