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缩宫素对大鼠肝脏缺血-再灌注损伤的保护作用及其机制
引用本文:陈杰,李相成,李长贤,许永华,张斌.缩宫素对大鼠肝脏缺血-再灌注损伤的保护作用及其机制[J].江苏医药,2010,36(5).
作者姓名:陈杰  李相成  李长贤  许永华  张斌
作者单位:南京医科大学第一附属医院肝脏移植中心,210029
基金项目:江苏省科教兴卫工程医学重点人才基金
摘    要:目的 探讨缩宫素对大鼠肝脏缺血-再灌注(I-R)损伤的保护作用及可能的机制.方法 将48只雌性SD大鼠随机均分为假手术(S)组、I-R组和缩宫素处理(OT)组.建立大鼠70%I-R模型,缺血时间1 h.OT组分别于术前12 h,15 min及再灌注时经腹腔注射缩官索0.5 mg/kg,S组及I-R组在相同时间注射等量生理盐水.各组大鼠分别于肝脏再灌注后2和6 h处死,取肝脏及血液标本,检测血清谷丙转氨酶(ALT)、谷草转氨酶(AST)、肿瘤坏死因子α(TNF-α)以及肝脏组织超氧化物歧化酶(SOD)、髓过氧化物酶(MPO)的活性及丙二醛(MDA)含量,并分别检测肝组织中核因子κB(NF-κB)的表达和肝脏组织的病理改变.结果 与I-R组相比,OT组的ALT、AST、TNF-α水平及MPO、NF-κB阳性表达明显降低(P<0.05),肝脏病理损伤较轻,但是MDA及SOD变化不明显.结论 缩宫素对大鼠肝脏I-R损伤具有保护作用.其机制可能与抑制炎症因子产生及活化有关.

关 键 词:缩宫素  缺血再灌注损伤  细胞因子

The protective effect and mechanism of oxytocin on hepatic ischemia-reperfusion injury in rats
Abstract:Objective To investigate the protective effect and mechanism of oxytocin against hepatic ischemia-reperfusion(I-R)injury in rats.Methods Forty-eight SD female rats were randomly divided into 3 groups of sham operation(S),I-R and oxytocin treatment(OT)with 16 rats each.The model of 70 % hepatic I-R was established by 1 h ischemia in groups of I-R and OT.Group OT was administered intraperitoneaUy OT 0.5 mg/kg at 12 h and 15 min before ischemia and immediately after reperfusion.Rats were killed at 2,6 h after reperfusion.The serum tumor necrosis factor-α(TNF-α)and transaminases(ALT,AST)were assayed.The superoxide dismutase(SOD),malondialdehyde (MDA)and myeloperoxidase(MPO)in liver tissues were measured.The expression of nuclear factor kappa B(NF-κB)in liver tissue was determined by immunohistochemistry,and histologic changes were observed by HE staining.Results Compared to group I-R,group OT was associated with lower serum ALT and AST,MPO activity,NF-κB expression(P<0.05).The injury of liver tissue in group OT was slighter.However,oxytocin treatment has litter effect on MDA and SOD activities(P>0.05).Conclusion The results suggest that oxytocin has a protective effect on hepatic I-R injury in rats.The mechanism of protection appears to be associated with its inhibiting the expressions of inflammatory eytokines.
Keywords:Oxytocin  Ischemia-reperfusion injury  Cytokines
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