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李郁,陈垦,徐在成,曾春雨.MG53在下肢远程缺血预适应保护肺缺血再灌注损伤中的作用[J].陆军军医大学学报(原第三军医大学学报),2015,37(05):409-413.
Li Yu,Chen Ken,Xu Zaicheng,Zeng Chunyu.Protective role of mitsugumin 53 in lung ischemic/reperfusion injury after limb remote ischemic preconditioning in rats[J].J Amry Med Univ (J Third Mil Med Univ),2015,37(05):409-413.
李郁,陈垦,徐在成,曾春雨.MG53在下肢远程缺血预适应保护肺缺血再灌注损伤中的作用[J].陆军军医大学学报(原第三军医大学学报),2015,37(05):409-413. DOI:
Li Yu,Chen Ken,Xu Zaicheng,Zeng Chunyu.Protective role of mitsugumin 53 in lung ischemic/reperfusion injury after limb remote ischemic preconditioning in rats[J].J Amry Med Univ (J Third Mil Med Univ),2015,37(05):409-413. DOI:
目的 研究MG53在下肢远程缺血预适应保护肺组织缺血再灌注损伤中的作用。 方法 肺缺血再灌注损伤模型通过开胸阻断左侧肺门进行缺血1 h后再灌注1 h建立。下肢远程缺血预适应模型是在进行肺缺血再灌注损伤前0.5 h阻断左侧股动脉血流5 min,然后再灌注5 min,重复3个循环来实现的。将60只10~12周龄SD大鼠[雌雄各半,体质量(235±15)g]采用完全随机分组方法分为3组(n=20):假手术组(sham组)、肺缺血再灌注损伤组(IR组)、下肢远程缺血预适应+肺缺血再灌注损伤组(RIP组)。将24只8~12周龄MG53敲除小鼠[雌雄各半,体质量(27.5±2.5)g]采用完全随机分组方法分为2组(n=12),即肺缺血再灌注损伤组(IR组)、下肢远程缺血预适应+肺缺血再灌注损伤组(RIP组)。在缺血及再灌注时间结束后,观察动脉氧分压、计算肺组织湿干比(W/D),通过Western blot检测3组之间肺组织上MG53蛋白表达量的改变,并记录其生存情况。 结果 对SD大鼠,在进行肺缺血再灌注损伤后其血氧分压降低到(46.60±5.94)mmHg,而下肢远程缺血预适应能显著改善肺组织的缺血再灌注损伤,使其血氧分压恢复至(73.40±5.94)mmHg(P0.05),同时对反映肺组织水肿程度的W/D值、生存情况都有显著的改善,通过Western blot方法检测到RIP组肺组织上MG53蛋白的表达量(2.03±0.53)较IR组(0.79±0.17)显著增加(P0.05)。在MG53敲除小鼠上,下肢远程缺血预适应组的血氧分压(48.20±12.15)mmHg较肺缺血再灌注损伤组(45.60±10.53)mmHg并未得到改善,同时也不能改善肺组织的水肿情况。 结论 MG53参与了下肢远程缺血预适应对肺组织缺血再灌注损伤的保护作用。
Objective To determine the role of mitsugumin 53 (MG53) in the protective effect of remote ischemic preconditioning (RIP) for lung ischemia/reperfusion (I/R) injury. Methods Lung ischemic/reperfusion injury model was established in SD rats by l
eft thoracotomy
clamped left hilum for 1 h
and then released for reperfusion for 1 h. For RIP
the left femoral artery was clamped for 5 min followed by being released for 5 min (this cycle was repeated for 3 times). This RIP procedure was done in 30 min before lung ischemic/reperfusion injury. SD rats (n=60) in both sexes (10 to 12 weeks old
weighting 235±15 g) were randomly divided into 3 groups
that is
sham group
IR group
and lung IR pretreated with RIP group. Male and female MG53 knockout mice (n=24) (8 to 12 weeks old
weighting 27.5±2.5 g) were divided into 2 groups
IR and RIP groups. After I/R period
the arterial blood samples were collected for arterial blood gas analysis
the lung tissues were obtained for measurement of wet/dry (W/D) ratio
and Western blot analysis was used for the protein expression of MG53. The survival rate were recorded and compared among the groups. Results In SD rats
lung I/R injury lowered PaO
2
to 46.60±5.94 mmHg
which was improved by pretreated with RIP
by increasing the value to 73.40±5.94 mmHg (P<0.05). At the same time
the W/D ratio and survival condition were also improved in RIP group than IR group. The expression of MG53 in the lung tissue was markedly increased in the former than the latter group (2.03±0.53 vs 0.79±0.17
P<0.05). However
all the protective effects
including the effect on PaO
2
were lost in the MG53 knockout mice. Conclusion MG53 participates in the protective effect of RIP against the lung ischemic/reperfusion injury.
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