期刊文献+

二氧化铈纳米颗粒对大鼠心肌缺血再灌注损伤的保护作用 被引量:4

Protective effects of CeO2 nanoparticles on the myocardial ischemia-reperfusion injury in rats
原文传递
导出
摘要 目的观察二氧化铈(CeO2)纳米颗粒对大鼠心肌缺血再灌注损伤的保护作用。方法将SD大鼠50只随机分为假手术组、模型组、1~10nm粒径组、10~25nm粒径组、50nm粒径组,每组10只,制作缺血再灌注模型。采用黄嘌呤氧化酶法和比色法分别测定超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GSH—Px)活性,硫代巴比妥酸法测定丙二醛(MDA)含量,同时观察心肌组织病理学和细胞凋亡。结果与假手术组比较,模型组SOD、GSH—Px活性明显下降,MDA含量明显升高(P〈0.05);与模型组比较,3种不同粒径组SOD、GSH—Px活性明显升高,MDA含量明显降低(P〈0.05)。3种不同粒径组心肌细胞凋亡指数[1—10nm组:(21.00±3.90)%;10~25nm组:(16.38±3.59)%;50nm组:(24.20±5.88)%]与模型组[(32.92±7.46)%]比较明显降低(P〈0.05)。结论二氧化铈纳米颗粒能减轻大鼠缺血再灌注心肌的氧化应激,具有较好的心肌保护作用。 Objective To investigate the protective effects of cerium oxide (CeO2 ) nanoparticles on myocardial ischemia-repeffusion injury in rats. Methods Fifty male Sprague-Dawley rats were randomly divided into five groups: sham group, experimental group and three preconditioning groups with different particle diameter [ 1-10 nm group, 10-25 nm group and 50 nm group ( n = 10 in each group) 1- The myocardial ischemia-repeffusion model was established successfully. The activities of superoxide dismutase (SOD) and glutathione (GSH) -Px, and the content of malondialdehyde (MDA) in myocardial tissue were determined. The morphology of myocardium was observed under a light microscope, and the apoptosis of myocardial cells was detected by using TdT-mediated dUTP nick end labeling (TUNEL) method. Results As compared with the Sham group, the activities of SOD and GSH-Px in experimental group were signifi- cantly decreased ( P 〈 0. 05 ) , while the content of MDA was increased ( P 〈 0. 05 ). The activities of SOD and GSH-Px were increased and the content of MDA was decreased in the three different particle diameter groups as compared with the experimental group ( P 〈 0. 05 ). The apoptosis of myocardial cells was significantly decreased in the three different particle diameter groups I (21.00 ± 3.90 )% for 1-10 nm group; ( 16. 38 ± 3.59 ) % for 10-25 nm group ; and ( 24. 20 ± 5.88 ) % for 50 nm group] as compared the experi- mental group [ (32. 92 ± 7.46) % ] ( P 〈 0. 05). Conclusion The CeO2 nanopartieles can protect the myocardium from isehemia-repeffusion injury by attenuating oxidative stress.
出处 《中华实验外科杂志》 CAS CSCD 北大核心 2014年第5期1060-1062,共3页 Chinese Journal of Experimental Surgery
基金 国家自然科学基金资助项目(81241003) 河南省科技创新杰出人才计划资助项目(104200510007) 郑州市科技创新人才培育计划资助项目(10LJRC175)
关键词 二氧化铈纳米颗粒 心肌缺血 再灌注损伤 心肌保护 CeO2 nanoparticles Myocardial ischemia Repeffusion injury Cardioprotection
  • 相关文献

参考文献11

  • 1Babu S, Velez A, Wozniak K, et al. Etecttron paramagnetic study on radical scavenging properties of ceria nanoparticles [ J ]. Chem Phys Lett, 2007,442 ( 4 -6 ) :405 -408.
  • 2Gao F,Lu Q, Komameni S. Fast synthesis of cerium oxide nanoparti- cles and nanorods [ J ]. J Nanosci Nanotechnol, 2006,6 ( 12 ) : 3812- 3819.
  • 3Schubert D, Dargusch R, Raitano J, et al. Cerium and yttrium oxide nanoparticles are neuroprotective [ J ]. Biochem Biophys Res Com- mun ,2006,342 ( 1 ) :86-91.
  • 4Das M, Patil S, Bhza'gava N, et al. Auto-catalytic eeria nanoparticles offer neuroprotection to adult rat spinal cord neurons [ J ]. Biomateri- als,2007 ,28(10) : 1918-1925.
  • 5Colon J,Hsieh N, Ferguson A, et al. Cerium oxide nanopartieles pro- tect gastrointestinal epithelium from radiation-induced damage by re- duction of reaction oxygen species and upregulation of superoxide dis- mutase 2[J]. Nanomedicine,2010,6(5) :698-705.
  • 6Liem DA, Honda HM,Zhang J, et aI. Past anti present course of ear- dioprotection against ischemia-repeffusion injury [ J ]. J Appl Physiol (1985) ,2007,103 (6) :2129-2136.
  • 7闫兴军,卢根林,邓勇.硫化氢在肠缺血-再灌注损伤大鼠肠黏膜屏障功能障碍中的作用[J].中华实验外科杂志,2010,27(1):71-74. 被引量:20
  • 8汪卫星,胡四平,孟志鹏,刘鹤,刘洋.缺血预处理对大鼠心肌细胞凋亡的影响及其机制[J].中华实验外科杂志,2010,27(2):237-238. 被引量:8
  • 9Yellon DM,Hausenloy DJ. Myocardial reperfusion injury[ Jj. N Engl J Med,2007,357(11) :1121-1135.
  • 10崔世涛,葛奎,徐兵,谢挺,牛轶雯,董炜,乔亮,姜育智.抗细胞间黏附分子-1抗体对心肌缺血再灌注损伤的保护作用[J].中华实验外科杂志,2008,25(1):86-88. 被引量:9

二级参考文献18

  • 1李敬远,朱珊珊,曾因明.不同浓度人参皂甙对大鼠离体心脏缺血再灌注损伤的保护作用[J].中华麻醉学杂志,2005,25(8):618-620. 被引量:6
  • 2耿彬,杜军保,唐朝枢北京大学第一医院心血管研究所.敏感硫电极法在测定心血管组织细胞及血浆胱硫醚-γ-裂解酶/硫化氢的应用[J].北京大学学报(医学版),2005,37(5):545-548. 被引量:86
  • 3黄克力,吴若彬,肖学钧,张锡彬,范瑞新.L-精氨酸对心肺移植缺血再灌注损伤的保护作用[J].中华实验外科杂志,2006,23(4):573-575. 被引量:16
  • 4朱红军,于曙东,何靖康,韩蓉,邬郡超,杨美菊,刘德森.前列腺素A1对兔供肺缺血再灌注损伤的保护作用[J].中华实验外科杂志,2007,24(3):277-278. 被引量:2
  • 5Yamamoto K, lto H, lwakura K, et al. Two different coronary blood flow velocity patterns in thrombolysis in myocardial infarction flow grade 2 in acute myocardial infarction : insight into mechanisms of microvascular dysfunction. J Am Coll Cardiol,2002,40 : 1755-1760.
  • 6Walther A, Czabanka M, Gebhard MM, et al. Glycoprotein ⅡB/ⅢA- inhibition and microcirculatory alterations during experimental endotoxemia-an intravital microscopic study in the rat. Microcirculation, 2004,11:79-88.
  • 7Kutala VK, Khan M, Angelos MG, et al. Role of oxygen in postischemic myocardial injury. Antioxid Redox Signal ,2007,9 : 1193-1206.
  • 8Tosa Y, Lee WP, Kollias N, et al. Monoclonal antibody to intercellular adhesion molecule 1 protects skin flaps against ischemia-reperfusion injury: an experimental study in rats. Plast Reconstr Surg, 1998,101 : 1586-1596.
  • 9Lille S, Boyle EM Jr, Schoeller T, et al. Augmentation of cAMP improves muscle-flap survival and tissue inflammation in response to ischemia/reperfusion injury. J Reconstr Microsurg, 1999,15:37-45.
  • 10Fiorucci S.Antonelli E,Distrutti E,et al.Inhibtion of hydrogen suliide generation contributes to gastric injury caused by anti-inflammatory non-steroidal drugs.Gastroenterology,2005,129:1210-1224.

共引文献34

同被引文献22

  • 1王全伟,凡文博,王智昊,吴扬.氧化应激与心血管疾病关系的研究进展[J].中国老年学杂志,2014,34(1):270-273. 被引量:61
  • 2Niu JL,Azfer A,Rogers LM,et al. Cardioprotective effects of cerium oxide nanopartieles in a transgenic murine model of cardiomyopathy [J]. Cardiovase Res,2007,73(3) :549-559.
  • 3Niu JL,Wang KK,Kolattukudy PE. Cerium oxide nanoparticles inhib- its oxidative stress and nuclear faetor-KB activation in H9c2 cardio- myocytes exposed to cigarette smoke extract [ J ]. J Pharmacol Exp T- her,2011,338( 1 ) :53-61.
  • 4Magesh S, Chen Y, Hu LQ. Small Molecule modulators of Keapl-Nrf2 - ARE pathway as potential preventive and therapeutic agents [ J ]. Med Res Rev,2012,32(4) :687-726.
  • 5Ngnyen T, Nioi P, Pickett CB. The Nrf2-antioxidant response element signaling pathway and its activation by oxidative stress [ J ]. J Biol Chem,2009,284(20) :13291-13295.
  • 6Kobayashi M, Yamamoto M. Molecular mechanisms activating the Nrf2-KeapI pathway of antioxidant gene regulation[ J]. Antioxid Red- ox Signal,2005,7(3) :385-394.
  • 7Tkachev VO, Menshehikova EB,Zenkov NK. Mechanism of the Nrf2/ Keapl/ARE signaling system [ J ]. Biochemistry Mosc ,2011,76 ( 4 ) : 407 -422.
  • 8Kong L, Cai X, Zhou X, et al. Nanoceria extend photoreeeptor cell li- fespan in tubby mice by modulation of apoptosis/survival signaling pathway[ J]. Neurobiol Dis ,2011,42(3 ) :514-523.
  • 9Zhou J, Chen Y, Huang GQ, et al. Hydrogen-rich saline reverses oxi- dative stress, cognitive impairment, and mortality in rats submitted to sepsis br' cecal ligation and puncture [ J ]. J Surg Res,2012,178 ( 1 ) : 390-400.
  • 10Zhou L, Wang X, Xue W, et al. Beneficial effects of hydrogen-rich sa- line against spinal cord ischemia-reperfusion injury in rabbits [ J ]. Brain Res,2013 ,1517 :150-160.

引证文献4

二级引证文献18

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