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作 者:臧秀娟[1] 宫丽[2] 洪海娟[1] 姜燕[1] 郑峰[1] 刘梅[1] 于青[2]
机构地区:[1]上海市松江区中心医院(上海交通大学附属第一人民医院松江分院)肾内科,201600 [2]上海交通大学附属第一人民医院肾内科
出 处:《中华肾脏病杂志》2012年第10期804-807,共4页Chinese Journal of Nephrology
基 金:基金项目:上海市卫生局局级科研课题(20114331);上海市松江区卫生局医学领先合作项目(2011)
摘 要:目的探讨中性粒细胞明胶酶相关脂质运载蛋白(NGAL)对大鼠缺血再灌注损伤。肾脏肾小管上皮细胞凋亡的保护作用及机制。方法建立大鼠肾脏缺血再灌注模型,雄性SD大鼠随机分为对照组、缺血再灌注模型组、NGAL组;HE染色观察3组大鼠肾组织病理变化;TUNEL法检测肾小管上皮细胞凋亡;实时定量PCR、Western印迹法检测凋亡蛋白fas、bcl-2的表达变化。结果与缺血再灌注模型组比较,NGAL组肾小管上皮细胞凋亡数量显著减少[(8.6+3.4)/HP比(20.8±3.7)/HP,P〈0.05];NGAL组肾组织fasmRNA(2.34+0.51比6.84±2.34,P〈0.05)、fas蛋白(0.65±0.05比0.95±0.08,P〈0.05)表达显著下调,bcl-2蛋白(0.33±0.05比0.24±0.03,P〈0.05)表达显著上调,但bcl-2mRNA表达无明显改变。结论NGAL对大鼠缺血再灌注损伤肾小管上皮细胞有保护作用,其作用可能与减少细胞凋亡、改变凋亡蛋白的表达有关。Objective To investigate the effects of neutrophil gelatinase associated !ipocalin(NGAL) on renal tubular epithelial cells apoptosis and apoptosis-regulated protein fas, bcl-2 in rat renal ischemia reperfusion injury (IRI). Methods Renal IRI models of rats were established. Rats were randomly divided into 3 groups, including control group, IRI model group and NGAL group. The pathological change of kidney tissue was investigated by hemotoxylin-eosin staining. Renal tubular epithelial cells apoptosis was detected by TUNEL method. Expression of fas and bcl-2 was measured by real-time PCR and Western blotting. Results Compared with IRI model group, NGAL group showed a decreased number of renal tubular epithelial cells apoptosis [(8.6±3.4)/HP vs (20.8±3.7)/HP, P〈0.05], down-regulated fas mRNA (2.34±0.51 vs 6.84±2.34, P〈 0.05), fas protein (0.65±0.05 vs 0.95±0.08, P〈0.05) and up-regulated bcl-2 protein (0.33± 0.05 vs 0.24±0.03, P〈0.05), but the bcl-2 mRNA had no significant change. Conclusion NGAL can protect renal tubular epithelial cells in renal IRI, which may be associated withdecreasing cell apoptosis and adjusting protein expression by apoptosis-regulated cytokines.
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