期刊文献+

阿霉素对围麻醉期心肌肌钙蛋白Ⅰ和心肌超微结构影响的实验研究 被引量:2

The effect of serum cardiac troponin Ⅰ level and myocardial ultrastructure on peri-anesthesia rats after Adriamycin chemotherapy
下载PDF
导出
摘要 目的研究阿霉素(ADM)化疗对大鼠围麻醉期心肌肌钙蛋白I(cTnI)水平、肌酸激酶(CK)和肌酸激酶同功酶(CKMB)活性的变化和心肌超微结构的影响,探讨围麻醉期心肌损伤的程度与特点。方法32只Wistar大鼠随机分成A、B、C、D组,每组8只。A、B组腹腔注射(ip)ADM2.50mg.kg-1,隔日1次,共6次(11d);C、D组ip相同容积的生理盐水。所有Wistar大鼠于最后一次注药后3d实施麻醉:A、C组选择吸入异氟烷麻醉;B、D组选择ip戊巴比妥钠麻醉。分别于麻醉前、麻醉后20min采血1ml,离心分离血清检测cTnI、CK和CKMB,并取出心脏制作病理和透射电镜标本。结果①4组Wistar大鼠麻醉前cTnI水平的差异无统计学意义,而麻醉后均有不同程度升高(P<0.01),A和B组、B和D组比较,差异均有统计学意义(P<0.01);B组麻醉前、后比较,差异有统计学意义(P<0.05);②4组Wistar大鼠麻醉前或后CK、CKMB值的差异均无统计学意义,麻醉前、后配对比较差异也无统计学意义(P均>0.05);③心肌病理改变:A、B组见心肌细胞变性、坏死;而C、D组结果正常,4组心肌组织病理评分差异有统计学意义(P<0.01)。结论cTnI是动态监测围麻醉期心肌损伤敏感的指标;是判断麻醉是否加重ADM化疗患者心肌损伤的重要标志。与戊巴比妥钠相比,吸入麻醉药异氟烷没有进一步加重ADM引起的心肌损伤,具有一定的心肌保护作用。 Objective To investigate the degree and characteristic of myocardial injury on peri-anesthesia wistar rats induced by Adriamycin (ADM) chemotherapy, through analysing the changes of serum cardiac troponin Ⅰ (cTnI) level, creatine kinase (CK) ,isoenzyme of creatine kinase (CKMB) activites and myocardial ultrastructure. Methods Thirty-two wistar rats were randomized into four groups : A, B, C and D. Rats in group A and B were treated with ADM by intraperitoneal injection ( ip), and rats in group C and D were treated with sodium chloride solution. All rats were treated with anesthesia on the third day after completing the last injection. Anesthesia treatment for the rats in group A and C were opened isoflurane inhalation, while for the rats in group B and D were sodium chloride pentobarbital solution by ip. Blood samples from all animal were taken at pre-anesthesia and 20min post-anaesthesia respectively. The hisptopathological changes of myocardium were observed with light microscope and transmission electron microscope. Results ①The differences of serum cTnl level among the four groups were not statistically significant at pre-anesthesia,but were statistically significant between group A and B ,group B and D at post-anesthesia (P 〈 0.01 ) . The cTnI levels in all of the four groups were higher at post-anesthesia than that at pre-anesthesia, with the statistical signifi- cance in Group B ( P 〈 0. 05 ). ②The levels of serum CK and CKMB between pre-anesthesia and post-anesthesia were not statistically significant in four groups (P 〉 0.05 ). ③ With light and electron transmission microscope, pathological changes of myocardi- um were significant between chemotherapy groups and control groups, as the severe cell degeneration and necrosis were observed in chemotherapy group. The histopathological score of myocardium was significantly different among the four groups. Conclusions Serum cTnI level is a sensitive marker of cardiac injury at peri-anesthesia,and it is more sensitive and specific than CK and CKMB levels. Serum cTnI level also is an important marker to evaluate aggravation of cardiac injury induced by anesthesia on ADM chemotherapy. Inhalation isoflurane have no significant effect on aggravating cardiac injury induced by ADM chemotherapy com- paried with sodium chloride pentobarbital,but provides certain degree of myocardial-protection effect.
出处 《中国癌症防治杂志》 CAS 2009年第3期203-207,共5页 CHINESE JOURNAL OF ONCOLOGY PREVENTION AND TREATMENT
基金 广西科技厅青年基金项目(桂科青NO0135003)
关键词 大鼠 阿霉素 心肌肌钙蛋白Ⅰ 肌酸激酶 肌酸激酶同功酶 心肌超微结构 心肌损伤 Rats Adriamycin Cardiac troponin Ⅰ Creatine kinase Isoenzyme of creafine kinase Myocardial ultrastructure Myoardial injury
  • 相关文献

参考文献7

二级参考文献35

  • 1杨军良,陈伯銮,赵树元,高仁果,高丽.不同麻醉方法对心率变异性的影响[J].中华麻醉学杂志,1995,15(1):5-9. 被引量:19
  • 2吕焕章,耿宝琴,朱永廉,雍定国.β-胡萝卜素对阿霉素所致的大鼠心脏毒性的作用(英文)[J].中国药理学报,1996,17(4):317-320. 被引量:11
  • 3王淑琴,黄汤汀,刘巍.阿霉素心脏毒性160例心电图分析[J].癌症,1990,9(6):494-496. 被引量:6
  • 4夏奕明 朱莲珍.血和组织中谷胱甘肽过氧化物酶活力的测定方法[J].卫生研究,1987,16(4):29-29.
  • 5陈顺志 金有余.过氧化脂质TBA显色的三种方法学比较[J].临床检验杂志,1984,2(4):8-8.
  • 6邓惠玲 张均田 见:徐叔云 卞如濂 陈修主编.超氧化物歧化酶测定[A].见:徐叔云,卞如濂,陈修主编.药理实验方法学:第:2版[C].北京:人民卫生出版社,1994.502-504.
  • 7Weinstein DM, Mihm MJ, Bauer JA. Cardiac peroxynitrite formation and left ventricular dysfunction following doxorubicin treatment in mice. J Pharmacol Exp Ther,2000;294(1):396~401
  • 8Misko TP, Moore WM, Kasten TP et al. Selective inhibition of the inducible nitric oxide synthase by aminoguanidine. Eur J Pharmacol, 1993;233(1):119~25
  • 9Ishiyama S, Hiroe M , Nishikawa T et al. Nitric oxide contributes to the progression of myocardial damage in experimental autoimmune myocarditis in rats. Circulation,1997;95(2):489~96
  • 10Bachmaier K, Neu N, Pummerer C et al. iNOS expression and nitrotyrosine formation in the myocardium in respone to inflammation is controlled by the interferon regulatory transcription factor 1. Circulation,1997;96(2)585~91

共引文献54

同被引文献19

  • 1贾艳华,吴荻.乳腺癌动物模型建立与应用的进展[J].中国肿瘤,2009,18(11):900-904. 被引量:6
  • 2阳冠明,孙胜涛,李树全,林伟雄,刘微,叶司原,利基林,林善修.β-胡萝卜素对阿霉素致大鼠心肌组织的超氧化物歧化酶、谷胱甘肽过氧化物酶mRNA表达改变的影响[J].中国药理学通报,2006,22(4):465-470. 被引量:20
  • 3彭玉娜,谭获,王颖超,区碧如,张还珠,黄振倩.阿霉素导致兔血清肌钙蛋白T变化的实验研究[J].国际医药卫生导报,2007,13(16):13-15. 被引量:3
  • 4Horowitz JD,Chirkov YY,Kennedy JA,et al. Modulation of myocar-dial metabolism: an emerging therapeutic principle[j].Curr OpinCardiol,2010,25(4) :329-334.
  • 5Kantor PF,Lucien A,Kozak R,et al.The antianginal drug trimetazi-dine shifts cardiac energy metabolism from fatty acid oxidation toglucose oxidation by inhibiting mitochondrial long-chain 3-ketoacylcoenzyme A thiolase[j].Circ Res,2000,86(5) :580-588.
  • 6Shi J,Abdelwahid E,Wei L. Apoptosis in anthracycline cardiomy-opathy[j].Curr Pediatr Rev,2011,7(4):329-336.
  • 7Iskesen I,Saribulbul 0,Cerrahoglu M,et al.Trimetazidine reducesoxidative stress in cardiac surgery[j].Circ J,2006,70(9): 1169-1173.
  • 8Lagadic-Gossmann D,Le Prigent K,Feuvray D-Effects of trimetazi-dine on pHi regulation in the rat isolated ventricular myocyte[j].BrJ Pharmacol, 1996,117(5):831-838.
  • 9Ruixing Y,Wenwu L,Al-Ghazali R. Trimetazidine inhibits car-diomyocyte apoptosis in a rabbit model of ischemia-reperfusion [ J ].Transl Res,2007,149(3): 152-160.
  • 10Fragasso G,Spoladore R,Cuko A, et al.Modulation of fatty acidsoxidation in heart failure by selective pharmacological inhibition of3-ketoacyl coenzyme-A thiolase[j].Curr Clin Pharmacol, 2007,2(3):190-196.

引证文献2

二级引证文献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