摘要
目的 研究缺血后处理对缺血-再灌注损伤(IRI)大鼠肺组织内IL-1β mRNA表达的影响并分析其可能的肺保护作用机制.方法 建立大鼠在体肺脏缺血-再灌注损伤模型,SD大鼠24只,随机分为假手术对照组(Sham组)、缺血-再灌注组(IR组)和缺血后处理组(IPostC组),每组8只.在体大鼠IR损伤模型制备完成,阻断左肺门终止血供及通气造成左肺缺血,达预定时间后松开阻断带恢复血供及通气,形成再灌注.Sham组将模型制备成功3 h后直接取标本 IR组缺血1 h后再灌注2 h IPostC组缺血1 h后给予重复3次的5 min灌注和5 min缺血的后处理,然后恢复血供及通气行再灌注1.5 h.实验结束后留取左肺组织制作10%的组织匀浆用于测定髓过氧化物酶(MPO)的含量 留取小块肺组织测定肺湿/干质量比(W/D),并在光镜下观察肺组织的病理变化 用RT-PCR法检测IL-1β m RNA的表达量. 结果与Sham组比较,IR组肺组织中IL-1β mRNA的表达量、MPO的活性及W/D值均明显升高(P〈0.05),病理学观察显示炎症反应明显加重 IPostC组肺组织中IL-1β mRNA的表达量、MPO的活性及W/D值与IR组相比均明显下降(P〈0.05),病理学观察显示炎症反应明显减轻 3组间比较,差异均有统计学意义(P〈0.05).结论 缺血后处理能够明显减轻鼠肺缺血-再灌注损伤,其机制可能与抑制缺血-再灌注损伤大鼠肺组织内IL-1β mRNA的表达有关.
Objective To investigate the effects of ischemic post - conditioning on lung IL - 1β mRNA expression during ischemia - reperfusion injury in rats and the possible mechanisms. Methods 24 rats were randomly allocated to three different groups ( n = 8, each group) after preparation of lung ischemia- reperfusion injury model. (1) Sham group : only Sham operation (thoracotomy) and no ischemia for 3 h. (2) Ischemia - reperfusion group ( IR group) : interruption of pulmonary perfusion and ventilation for 1 h followed by reperfusion for 2 h. (3) Ischemic post - conditioning group ( IPostC group): ischemic post -conditioning (5R/51, three times) between the end of ischemia and the beginning of reperfusion followed by reperfusion for 1.5 h. Small pieces of lung tissue ( about 20 mg) were made into homogenate at the end of experiment. The concentration of MPO in the homogenate was determined. The wet to dry weight ratio (W/D) was also measured at the end of reperfusion. The lung tissue was prepared for light microscopic observation after reperfusion. RT - PCR was used to detect the expression of IL - 1β mRNA in lung tissue. Results There was significant statistical difference among three groups( P 〈 0. 05 ). The expression of IL - 1β mRNA, the levels of MPO and W/D significantly increased in IR group compared to Sham group (P 〈 0. 05 ) ;the lung histological examination showed that the inflammation of the lung in IR group was significantly serious than that in Sham group. The expression of IL - 1β mRNA ,the levels of MPO and W/D in the lung in IPostC group were significantly decreased compared to IR group ( P 〈 O. 05 ) ; the lung histological examination showed that the inflammation of the lung in IPostC group was significant compared to IR group. Conclusion Ischemic post - conditioning can significantly reduce lung ischemia - reperfusion injury by inhibiting the expression of IL - 1β mRNA in the lung possibly.
出处
《中国急救医学》
CAS
CSCD
北大核心
2010年第11期1008-1011,1057,共5页
Chinese Journal of Critical Care Medicine
基金
基金项目:贵州省科学技术基金资助项目(黔科合J字[2009]2313号)