Department of Thoracic Surgery, Subei People's Hospital of Jiangsu province, Yangzhou 225001, Jiangsu, PR China.
Pulm Pharmacol Ther. 2012 Feb;25(1):99-103. doi: 10.1016/j.pupt.2011.12.006. Epub 2011 Dec 27.
Neutrophil elastases (NE) play an important role in the pathogenesis of acute lung injury (ALI). NE activities are significantly increased in serums and lungs of patients or animals with ALI. Intravenous infusion (IV) of Sivelestat, an NE inhibitor, can reduce ALI. Through inhalation, drugs reach lungs directly and in high concentration. We hypothesized that inhaled Sivelestat would alleviate oleic acid (OA)-induced ALI in rats.
Rats were anesthetized and mechanically ventilated, and then ALI was induced by OA injection. One hour later, the animals were randomized to receive either Sivelestat (3 mg/kg/h) or saline inhalation. The effect of Sivelestat IV (3 mg/kg/h) was also investigated. All animals were ventilated and observed for 6 h.
OA injection increased NE activities in lung tissues and serums. The increase of NE activities in lung tissues and serums markedly reduced by 77%, and 29%, respectively, by the inhalation of Sivelestat; and 53.8%, and 80%, respectively, by Sivelestat IV. Additionally, inhaled Sivelestat resulted in ameliorated lung injury by reducing edema and infiltration of neutrophils in the lung, improved oxygenation and survival.
An over increased NE activity in lungs may play a vital effect in the pathogenesis of OA-induced ALI in rats. Topical application of nebulized Sivelestat, an NE inhibitor, may reduce OA-induced ALI in rats. Sivelestat inhalation can be developed as a novel treatment for ALI.
中性粒细胞弹性蛋白酶(NE)在急性肺损伤(ALI)发病机制中起重要作用。ALI 患者或动物的血清和肺组织中 NE 活性显著增加。NE 抑制剂西维来司他静脉输注(IV)可减轻 ALI。通过吸入,药物可直接到达肺部并达到高浓度。我们假设吸入西维来司他可减轻油酸(OA)诱导的大鼠 ALI。
大鼠麻醉并机械通气,然后用 OA 注射诱导 ALI。1 小时后,动物随机接受西维来司他(3mg/kg/h)或生理盐水吸入。还研究了西维来司他 IV(3mg/kg/h)的效果。所有动物均进行通气并观察 6 小时。
OA 注射增加了肺组织和血清中的 NE 活性。西维来司他吸入使肺组织和血清中的 NE 活性分别显著降低 77%和 29%;西维来司他 IV 使 NE 活性分别降低 53.8%和 80%。此外,吸入西维来司他通过减少肺组织水肿和中性粒细胞浸润,改善氧合和存活率,减轻了肺损伤。
肺内 NE 活性过度增加可能在 OA 诱导的大鼠 ALI 发病机制中起重要作用。NE 抑制剂雾化西维来司他的局部应用可能减轻 OA 诱导的大鼠 ALI。吸入西维来司他可作为一种新型 ALI 治疗方法。