期刊文献+

Omi/HtrA2抑制剂对肾脏缺血再灌注损伤诱导的肾小管上皮细胞凋亡的影响 被引量:1

Effect of Omi/HtrA2 inhibitor on tubular cell apoptosis induced by renal ischemia/reperfusion injury in rats
暂未订购
导出
摘要 目的研究Omi/HtrA2抑制剂(UCF-101)对大鼠肾脏缺血/再灌注(I/R)损伤诱导的肾小管上皮细胞凋亡的影响。方法雄性Wistar大鼠随机分为5组:假手术组(DMSO)、模型1组(I/R+R前DMSO)、模型2组(I/R+R后DMSO)、治疗1组(I/R+R前UCF-101)和治疗2组(I/R+R后UCF-101)。双侧肾动脉夹闭45min再灌注24h制作动物模型;比色法测定血清肌酐和尿素氮浓度;Western blot法检测肾组织中天冬氨酸特异性半胱氨酸蛋白酶(caspase)-3、caspase-9的蛋白质表达;原位末端标记TUNEL法检测肾小管上皮细胞凋亡。结果肾脏缺血45min再灌注24h后,大鼠肾功能明显减退(P<0.05);肾组织中caspase-3、caspase-9蛋白质表达显著增加(P<0.05),大量肾小管上皮细胞凋亡(P<0.05)。再灌注前给予UCF-101能显著改善肾功能(P<0.05),并显著下调caspase-3、caspase-9蛋白质表达(P<0.05),减轻肾小管上皮细胞凋亡(P<0.05),而再灌注后给药不能改善肾功能及caspase-3、caspase-9蛋白质的表达(P>0.05)。结论再灌注前给予UCF-101能抑制肾脏I/R损伤诱导的肾小管上皮细胞凋亡,对肾脏I/R损伤具有保护作用。 Objective To investigate the effect of UCF-101, an Omi/HtrA2 inhibitor, on tubular cell apoptosis induced by renal ischemia/reperfusion injury in rats. Methods Male Wistar rats were randomly divided into the follow ing five groups: sham group (DMSO alone), model group 1 (I/R plus DMSO before reperfusion), model group 2 (I/R plus DMSO after reperfusion), treatment group 1 (I/R plus UCF101 before reperfusion) and treatment group 2 (I/R plus UCFIO1 after reperfusion). Renal FRI models were established by clamping both renal arteries for 45 rain and reperfusion for 24 h. The level of serum creatinine (Set) and blood urea nitrogen (BUN) were measured by colorimetry, protein expressions of renal cysteinyl aspartate--specific protease (caspase)-3 and caspase-9 were detected by western blotting. Tubular cell apoptosis was confirmed by terminal deoxynucleotidyl transferase (TDT)-mediated dUTP-biotin nick end labeling (TUNEL) assay. Results Renal I/R injury induced significant increases in Scr and BUN (P〈O.05), tubular cell apoptosis (P〈0.05) and protein expressions of easpase-3 and caspase-9 (P〈0.05). Use of UCF-101 10 rain before repeffusion was found to markedly improve renal function (P〈O.05), decrease tubular cell apoptosis (P〈0.05) and the expressions of caspase-3 and caspase- 9 (P〈0.05), while UCF-101 administered at 1 h after reperfusion did not show any effects on renal function (P〉0.05), tubular cell apoptosis (P〉0.05) and the expressions ofcaspase-3 and caspase-9 (P〉0.05). Conclusion UCF-101 appeared to suppress tubular cell apoptosis induced by renal I/R injury and protect renal function.
出处 《中国药物与临床》 CAS 2009年第6期465-468,共4页 Chinese Remedies & Clinics
基金 山西省自然科学基金(2008011078-1) 山西医科大学第二医院博士启动基金(20070402)
关键词 再灌注损伤 细胞凋亡 大鼠 Reperfusioninjury Kidney Apoptosis Rats
  • 相关文献

参考文献12

  • 1Lameire N,van Biesen W,Vanhoider R.Acute renal failure.Lancet,2005,365 (9457):417-430.
  • 2Juang YT,Solomou EE,Rellahan B,et al.Phosphorylation and O-linked glycosylation of Elf-1 leads to its transiocation to the nucleus and binding to the promoter of the TCR zeta-chain.J Immunol,2002,168:2865-2871.
  • 3Suzuki Y,Takahashi-Nk K,Akagi T,et al.Mitochondrial protease Omi/HtrA2 enhances caspase activation through multiple pathways.Cell Death Differ,2004,11 (2):208-216.
  • 4Liu HR,Gao E,Hu A,et al.Role of omi/HtrA2 in apoptotic cell death after myocardial ischemia and reperfusian.Circulation,2005,111:90-96.
  • 5Padanilam BJ.Cell death induced by acute renal injury:a perspective on the contributions of apoptnsis and necrosis.Am J Physiol Renal Physiol,2003,284:608-627.
  • 6Rassig L,Haendeler J,Mallat Z,et al.Congestive heart failure induces endothelial cell apoptosis:protective role of carvedilol.J Am Coll Cardiol,2000,36(7):2081-2089.
  • 7Gray CW,Ward RV,Karran E,et al.Characterization of human HtrA2:a novel serine protease involved in the mammalian cellular stress response.Eur J Biochem,2000,267 (18):5699-5710.
  • 8Hegde R,Srinivasula SM,Zhang Z,et al.Identification of Omi/HtrA2 as a mitochondrial apoptotic serine protease that disrupts inhibitor of apoptosis protein-caspase interaction.J Biol Chem,2002,77:432-438.
  • 9Bhuiyan MS,Fukunaga K.Inhibition of HtrA2/Omi ameliorutes heart dysfunction following ischemia/reperfusion injury in rat heart in vivo.Eur J Pharmacology,2007,557:168-177.
  • 10Althaus J,Sieqelin MD,Dehqhani F,et al.The serine protease Omi/HtrA2 is involved in XIAP cleavage and in neuronal cell death following focal cerebral ischemia/reperfusion.Neurochem Int,2007,50(1):172-180.

二级参考文献15

  • 1王晓樑,王瑾,吕小萍,王澎,刘慧荣.线粒体丝氨酸蛋白酶Omi/HtrA2与细胞凋亡[J].生理科学进展,2006,37(3):285-288. 被引量:7
  • 2徐宗全,陈孝平,李常海,李高鹏,张志发.线粒体促凋亡因子Omi/HtrA2在肝癌组织中表达的研究[J].中国组织化学与细胞化学杂志,2006,15(6):617-622. 被引量:7
  • 3Stevens PE, Tamimi NA, Al-Hasani MK, et al. Non-specialist management of acute renal failure. QJM, 2001, 94(10):533-540.
  • 4Lameire N, van Biesen W, Vanholder R. Acute renal failure. Lancet, 2005, 365(9457): 417-430.
  • 5Meldrum K, Meldrum D, Hile K, et al. A novel model of ischemia in renal tubular cells which closely parallels in vivo injury. J Surg Res, 2001, 99: 288-293.
  • 6Padanilam BJ. Cell death induced by acute renal injury: a perspective on the contributions of apoptosis and necrosis. Am J Physiol Renal Physiol, 2003, 284: 608-617.
  • 7Hannon GJ. RNA interferenee. Nature, 2002, 418(6894):244- 251.
  • 8Hu XY, Chen XC, Ping H, et al. Immunohistochemical analysis of Omi/HtrA2 expresslon in prostate cancer and benign prostatic hypellolasia. APMIS, 2006, 114(12):893-898.
  • 9Hentsehel DM, Park KM, Cilenti L, et al. Acute renal failure in zebrafish: a novel system to study a complex disease. Am J Physiol Renal Physiol, 2005, 288(5): 923-929.
  • 10Kuninaka S, Nomura M, Hirota T, et al. The tumor suppressor WARTS activates the Omi/HtrA2-dependent pathway of cell death. Oncogene, 2005, 24(34): 5287-5298.

同被引文献3

引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部