摘要
目的:探讨P选择素及其单克隆抗体在肝、肾缺血再灌注时其表达对细胞凋亡的影响。方法:建立大鼠肝及肾缺血再灌注损伤模型,分别采用免疫组化链菌素抗生物素蛋白生物素酶标法和原位DNA片断末端标记法检测有或无P选择素单抗治疗组肝、肾组织中P选择素表达及凋亡细胞。结果:大鼠肝、肾缺血再灌注时P选择素在肝、肾内广泛表达,肝、肾组织出现显著病理改变并发生细胞凋亡;P选择素单抗作用组肝、肾组织中P选择素未表达,无明显病理变化且细胞凋亡减少。结论:在肝、肾缺血再灌注时,P选择素介导了肝、肾内中性粒细胞积聚和细胞凋亡,并加重肝、肾损伤;抑制P选择素可减少肝、肾内中性粒细胞积聚和细胞凋亡,减轻肝。
Objective:To evaluate the potential role of Pselectin in apoptosis during liver and renal ischemiareperfusion injury.Methods:Pselectin expression and cell apoptosis were detected in rat liver or renal ischemiareperfusion model by immunohistochemistry and terminal deoxynucleotidy transferase mediated dUTPbiotin nickend labeling(TUNEL).Results:Pselectin expression,pathological lesions and cell apoptosis were found in liver and renal tissues following liver and renal ischemiareperfusion injury,and these changes became less conspicuous in animals treated with antiPselectin monoclonal antibody.Conclusions: Pselectin might mediate neutrophil infiltration and cell apoptosis and contribute to liver and renal ischemiareperfusion injury.Inhibition of Pselectin may decrease neutrophil infiltration and cell apoptosis,thus mitigating ischemiareperfusion injury of liver and renal.
出处
《中国危重病急救医学》
CAS
CSCD
1999年第4期213-215,共3页
Chinese Critical Care Medicine
基金
卫生部科研基金
上海市自然科学基金
关键词
缺血
再灌注损伤
细胞凋亡
P选择素
ischemiareperfusion injury\ \ apoptosis\ \ Pselectin\ \ Pselectin monoclonal antibody