银杏总黄酮对肾缺血再灌注大鼠p-JNK表达的影响(朱家军等).docVIP

银杏总黄酮对肾缺血再灌注大鼠p-JNK表达的影响(朱家军等).doc

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银杏总黄酮对肾缺血再灌注大鼠p-JNK表达的影响(朱家军等)

银杏总黄酮对肾缺血再灌注大鼠p-JNK表达的影响 朱家军1,夏安周2,王妍妍2,张探2, 李娜2 (1.灌云县人民医院,江苏灌云222200.徐州医学院,江苏徐州221004;) [摘要] 目的: 观察肾缺血再灌注损伤(IRI)后JNK活化的变化,并探讨银杏总黄酮(TFG)对其影响。方法: SD大鼠随机分为假手术组(Sham,n = 12)、缺血再灌注组(IR,n = 30)和银杏总黄酮处理组(TFG,n = 12)。采用夹闭双侧肾动静脉45 min然后松开动脉夹制备肾IRI模型。蛋白免疫印迹检测肾组织中p-JNK的表达,并用细胞凋亡原位末端标记(TUNEL法)检测肾小管上皮细胞凋亡。结果: IR组肾组织中p-JNK的表达在再灌注10 min 开始升高,再灌注30 min 达到高峰,再灌注1h有所降低,再灌注24h再次升高,同时该时段有大量肾小管上皮细胞凋亡;给予TFG处理,再灌注30min p-JNK表达明显减弱,再灌注24h细胞凋亡明显减少。结论:TFG 防治肾IRI机制可能与抑制??组织中JNK磷酸化的程度,减少肾小管上皮细胞凋亡有关。 [关键词] 缺血再灌注;银杏总黄酮;c-Jun 氨基末端激酶;肾 Effect of total flavone of Gingko on phosphorylation of JNK in rats with renal ischemia-reperfusion injury XIAAn-zhou1, ZHUJia-jun2 *, WANGYan-yan1,ZHANGTan1 ,LINa1 (1 Department of pharmacology , Xuzhou Medical college , Xuzhou 221002;2 Department of Anesthesiology, the People’s Hospital of Guanyunxian , Jiangsu, Lianyungang 222004) Abstract:Objective To investigate the change of phosphorylation of JNK in renal ischemia reperfusion injury(IRI)and study the effect of total flavone of Gingko(TFG)on JNK activation. Methods Male Sprague-Dawley rats were randomly divided into sham-operation group(Sham, n =12),ischemia reperfusion groups(IR, n=30) and TFG groups(TFG, n=12). The models?were?established through clamping bilateral renal arteries for 45 min?and then reperfusion. Tubular cell apoptosis was confirmed by terminal deoxynucleotidyl transferase (TDT)-mediated dUTP-biotin nick end labeling (TUNEL) assay;The phosphorylation of JNK were detected by Western blotting analysis. Results In the IR group, the levels of tubular cell apoptosis were significantly increased; activation of JNK was observed in the kidney as early as 10 min after reperfusion,reaching its peak at 30 min and declined at 1 h,but increasd at 24 h after reperfusion. pretreatment with TFG decreased significantly the levels of tubular cell apoptosis; it also decreased the phosphorylation level of JNK compared with that in the IR group. Conclusion The results showed that the mechanism of TFG to pro

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