Sivelestat, a specific neutrophil elastase inhibitor, prevented phorbol myristate acetate-induced acute lung injury in conscious rabbits

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• 作者：Hagio ; T. ; Matsumoto ; S. ; Nakao ; S. ; Matsuoka ; S. ; Kawabata ; K.
• 关键词：Elastase ; Acute lung injury ; Sivelestat ; Phorbol myristate acetate
• 刊名：Pulmonary Pharmacology & Therapeutics
• 出版年：2005
• 出版时间：August, 2005
• 年：2005
• 卷：18
• 期：4
• 页码：285-290
• 全文大小：262 K

文摘

The in vivo contribution of neutrophil elastase (NE) in phorbol myristate acetate (PMA)-induced acute lung injury has so far been unclear. This study examined the role of NE in PMA-induced acute lung injury in conscious rabbits, using a specific NE inhibitor, sivelestat sodium hydrate (Sivelestat). A single bolus injection of PMA (40μg/kg) caused acute lung injury as indicated by an increase in protein concentration and hemorrhage in bronchoalveolar lavage fluid (BALF) 4h after PMA injection. These changes were associated with mild decrease in arterial oxygen pressure and peripheral white blood cell and platelet. When continuously infused starting 1h before and ending 4h post-PMA injection, Sivelestat at 3–30mg/kg/h that are able to inhibit rabbit NE activity by 60–90 % , dose-dependently attenuated both PMA-induced hemorrhagic pneumonitis and the increase in protein concentration in BALF without affecting myeloperoxidase activity in the lung. Histopathological study indicated that sivelestat (30mg/kg/h) markedly attenuated lung histopathological changes, alveolar hemorrhage and white blood cells migration with evidence of inhibition of NE activity in BALF. These results suggest that NE plays a significant role in PMA-induced acute lung injury and further supports the importance of this enzyme in acute lung injury.