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机构地区:[1]中国医科大学附属第四医院消化内科,辽宁沈阳110032 [2]中国医科大学附属第四医院肿瘤放射治疗科 [3]吉林大学附属第一医院小儿外科
出 处:《中国医科大学学报》2007年第1期27-29,共3页Journal of China Medical University
基 金:吉林省计委科技攻关基金资助项目(1997-65)
摘 要:目的:探讨双嘧达莫(DP)预处理对大鼠原位肝移植缺血再灌注损伤(IRI)的保护作用及机制。方法:建立大鼠原位肝移植动物模型,应用不同剂量DP(B组:0.1mg·kg-1、C组:0.2mg·kg-1、D组:0.4mg·kg-1)进行预处理,并与盐水预处理组(A组)进行对照,分别检测移植前、移植后6h血清肝酶谱及移植前、移植后1h及6h肝组织一氧化氮(NO)、髓过氧化物酶(MPO)水平。结果:C、D组与A组比较能明显降低移植后血清肝脏酶学水平、增加组织内NO水平、降低MPO水平(P<0.01),C组作用更为明显。结论:DP预处理能够对大鼠原位肝移植的IRI产生保护作用。Objective: To evaluate the protective effect of dipyridamole (DP) preconditioning on isehemia/reperfusion injury in rat orthotopie liver transplantation and to explore the mechanism. Methods: The rat model of orthotopic liver transplantation was established. The rots were treated with normal saline (group A),0.1 mg·kg^-1 DP (group B),0.2 mg·kg^-1 DP (group C),and 0.4 mg·kg^-1 DP (group D),respectively. The levels of alanine aminotransferase and aspartate aminotransferase in serum were measured before and 6 hours after transplantation,and the levels of nitric oxide and myeloperoxidase in liver tissue were detected before and 1 and 6 hours after transplantation. Results:Compared with group A,the level of nitric oxide significantly increased and the levels of alanine aminotrasferase,asparatate aminotransferase,and myleoperoxidase significantly decreased in groups C and D (all P 〈 0.01). Compared with group D,the changes in the levels of the substances mentioned above were more significant in group C. Condusion:DP preconditioning could protect the liver against ischemia/reperfusion injury in rat orthotopic liver transplantation.
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