摘要
目的:观察内毒素致兔急性肺损伤(ALI)时血清血管紧张素转换酶(ACE)活性和肺组织内皮素-1(ET-1)含量变化及美洛昔康对急性肺损伤干预作用的机制。方法:将24只日本大耳白兔随机分为对照组、致伤组、美洛昔康干预组。用内毒素(700μg/kg)一次性静脉注射方法复制兔ALI模型,应用美洛昔康(2.5 mg/kg)进行干预。分别检测血清ACE活性和肺组织ET-1含量。结果:致伤后0.5 h,血清ACE活性明显升高,1 h时血清ACE活性达到峰值。美洛昔康组血清ACE活性也出现升高,但明显低于致伤组。致伤组肺组织ET-1高于对照组(P<0.01),美洛昔康干预组肺组织ET-1明显低于致伤组(P<0.01)。结论:美洛昔康可以抑制血清ACE活性和降低肺组织中ET-1的含量,对内毒素所致ALI具有一定的拮抗作用。
Objective :To investigate the changes of serum angiotensin converting enzyme (ACE)activity and pulmonary endothelin-1 (ET-1) content in rabbits with acute lung injury (ALI) induced by endotoxin and the effects of meloxicam, so as to explore the protective mechanism of meloxicam. Methods:Twenty four Japanese flap-eared white rabbits were randomly assigned to three groups : control group, endotoxin -treated group and meloxicam -treated group. ALI models of rabbits were replicated with intravascular endotoxin injection (700 μg/kg weight), meloxicam (2.5 mg/kg weight) was intravascularly injected in treatment group. We measured serum ACE activity and pulmonary ET-1 content in every group. Results:In endotoxin-treated group, serum ACE activity increased at 0.5h,and reached a peak at lh. In meloxicam-treated group, ACE activity in serum also increased,while serum ACE activity was significantly lower than that in endotoxin-treated group. In endotoxin - treated group, the levels of ET-1 in lung tissue were significantly higher than those in control group(P 〈0.01 ). In meloxicam-treated group, the levels of ET-1 in lung tissue were significantly lower than those in endotoxin -treated group(P 〈 0.01 ). Conclusion: Meloxicam can inhibit serum ACE activity and down-regulate the levels of ET in lung tissue, which pesseses some protective effects on ALI induced by endotoxin in rabbits.
出处
《军医进修学院学报》
CAS
北大核心
2007年第3期225-227,共3页
Academic Journal of Pla Postgraduate Medical School
基金
军队医药卫生科研基金(01MA114)