促红细胞生成素对大鼠体外循环后肾脏保护作用的研究

胡健, 殷仕宝, 叶阿奇, 钱云, 李德闽

胡健, 殷仕宝, 叶阿奇, 钱云, 李德闽. 促红细胞生成素对大鼠体外循环后肾脏保护作用的研究[J]. 实用临床医药杂志, 2013, (9): 9-12. DOI: 10.7619/jcmp.201309003
引用本文: 胡健, 殷仕宝, 叶阿奇, 钱云, 李德闽. 促红细胞生成素对大鼠体外循环后肾脏保护作用的研究[J]. 实用临床医药杂志, 2013, (9): 9-12. DOI: 10.7619/jcmp.201309003
HU Jian, YIN Shibao, YE Aqi, QIAN Yun, LI Demin. Protective effect of erythropoietin on renal injury following cardiopulmonary bypass in rats[J]. Journal of Clinical Medicine in Practice, 2013, (9): 9-12. DOI: 10.7619/jcmp.201309003
Citation: HU Jian, YIN Shibao, YE Aqi, QIAN Yun, LI Demin. Protective effect of erythropoietin on renal injury following cardiopulmonary bypass in rats[J]. Journal of Clinical Medicine in Practice, 2013, (9): 9-12. DOI: 10.7619/jcmp.201309003

促红细胞生成素对大鼠体外循环后肾脏保护作用的研究

详细信息
  • 中图分类号: R692

Protective effect of erythropoietin on renal injury following cardiopulmonary bypass in rats

  • 摘要: 目的 研究促红细胞生成素(EPO)对于大鼠体外循环(CPB)术后肾脏损伤的保护作用并探讨其相关机制.方法 将30只雄性SD大鼠随机均分为Sham组、CPB组及EPO组,每组10只.Sham组建立CPB模型管道,不进行CPB;其他2组建立CPB,以最大流量≥100 mL/(kg·min)转流维持1h,其中EPO组于转流前在预充液中加入EPO 3000U/kg.分别于肝素化后转流前(T0)、转流结束后(T1)和转流结束后0.5 (T2)、1(T3)、2(T4)、24 h(T5)检测血清肌酐(SCr)、尿素氮(BUN)水平;T5时取肾脏组织,检测组织肿瘤坏死因子(TNF-α)、白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)等炎症因子水平;同时测定肾脏组织丙二醛(MDA)、过氧化氢酶(CAT)、超氧化物歧化酶(SOD)等氧化应激指标水平,并行HE染色观察组织形态学改变.结果 T0时3组SCr、BUN水平无显著差异;与CPB组相比,EPO组T1至T5各时间点SCr、BUN水平明显下降(P<0.05),肾组织中TNF-a、IL-1β、IL-6等炎症因子水平均明显低于CPB组(P <0.05);CPB组MDA高于Sham组,CAT、SOD活性则较Sham组低;EPO组CAT、SOD活性高于Sham组;组织病理学检查显示,EPO组的肾小管上皮细胞肿胀、胞浆内空泡形成、间质出血等病理变化较CPB组明显减轻(P<0.05).结论 EPO可能通过抑制炎症因子的表达,降低氧化应激损伤,达到减轻CPB后肾脏损伤的目的.
  • Thakar C V, Arrigain S, Worley S. A clinical score to predict acute renal failure after cardiac surgery [J]. Journal of the American Society of Nephrology, 2005(1):162.
    Provenchere S, Plantefeve G, Hufnagel G. Renal dysfunction after cardiac urgery with normothermic cardiopulmonary bypass:incidence, risk factors, and effect on clinical outcome [J]. Anesthesia and Analgesia, 2003(5):1258.
    Villa P, Bigini P, Mennini T. Erythropoietin selectively attenuates cytokine production and inflammation in cerebral ischemia by targeting neuronal apoptosis [J]. Journal of Experimental Medicine, 2003(6):971.
    Patel N S, Sharples E J, Cuzzocrea S. Pretreatment with EPO reduces the injury and dysfunction caused by ischemia/reperfusion in the mouse kidney in vivo [J]. Kidney International, 2004(3):983.
    黄海嵘, 王常田, 申翼. 体外循环后大鼠肝损伤的研究 [J]. 医学研究生学报, 2009(1):32.doi: 10.3969/j.issn.1008-8199.2009.01.009.
    Zhu J, Yin R, Shao H. N-acetylcysteine to ameliorate acute renal injury in a rat cardiopulmonary bypass model [J]. Journal of Thoracic and Cardiovascular Surgery, 2007(3):696.
    王常田, 申翼, 钱雅君. 心肺转流对大鼠血浆和肺内基质金属蛋白酶-9的影响 [J]. 医学研究生学报, 2011(3):242.doi: 10.3969/j.issn.1008-8199.2011.03.004.
    Wang Z, Zhang J, Liu H. Melatonin, a potent regulator of hemeoxygenase-1, reduces cardiopulmonary bypass-induced renal damage in rats [J]. Journal of Pineal Research, 2009(3):248.
    Ates E, Yalcin A U, Yilmaz S. Protective effect of erythropoietin on renal ischemia and reperfusion injury [J]. Anz Journal of Surgery, 2005, (12):1100.
    Paparella D, Yau T M, Young E. Cardiopulmonary bypass induced inflammation:pathophysiology and treatment.An update [J]. European Journal of Cardio-Thoracic Surgery, 2002(2):232.
    Westaby S, Saatvedt K, White S. Is there a relationship between cognitive dysfunction and systemic inflammatory response after cardiopulmonary bypass [J]. Annals of Thoracic Surgery, 2001(2):667.
    Jaeschke H. Molecular mechanisms of hepatic ischemia-reperfusion injury and preconditioning [J]. American Journal of Physiology-Gastrointestinal and Liver Physiology, 2003(1):15.
计量
  • 文章访问数:  262
  • HTML全文浏览量:  24
  • PDF下载量:  9
  • 被引次数: 0
出版历程
  • 发布日期:  2013-10-17

目录

    /

    返回文章
    返回
    x 关闭 永久关闭