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制备小鼠病毒性心肌炎模型最适柯萨奇病毒B_3浓度的实验研究 被引量:7

Study on optimal virus concentration to establish the murine viral myocarditis model of Coxsackievirus B_3
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摘要 目的寻找制备病毒性心肌炎模型的最适病毒浓度,为筛选治疗病毒性心肌炎药物提供实验模型。方法采用柯萨奇病毒B(3CVB3)Nancy株,经腹腔注射,感染BALB/C小鼠。按注射病毒浓度的不同将75只小鼠分为4组:A组20只,注射高浓度CVB(3104TCID50);B组20只,注射中等浓度CVB(3102TCID50);C组20只,注射低浓度CVB(3100TCID50);D组15只,作为正常对照组。接种后第7d随机从各组取5只小鼠,眼眶取血后处死,称重,并留取心脏标本,将剩余小鼠喂养至第21d,然后将存活小鼠全部处死。观察4组小鼠的发病特征、死亡率、心脏组织病理学变化、心脏重量/身体重量(HW/BW)比值以及血清肌酸激酶同工酶(CK-Mb)水平。结果A组小鼠症状明显较其他3组严重,死亡率达100.0%,高于其他3组,B组死亡率显著高于C组;第7d,A组HW/BW比值、心肌病理评分以及CK-Mb水平均明显高于其他3组,B组HW/BW比值、心肌病理评分以及CK-Mb水平均显著高于C组。结论小鼠的死亡率、心肌病理评分以及CK-Mb水平与接种病毒浓度密切相关,本实验制备病毒性心肌炎小鼠模型最适病毒浓度为102TCID50。 Objective To investigate the dosage of Coxsackievirus B3 for establishing murine myocarditis model. Methods BALB/C mice were intraperitoneally inoculated with different dilution of CVB3. Seventy five mice were divided into 4 groups: high dosage group (10^3TCID50), middle dosage group (10^3TCID50), lower dosage group (10^3TCID50), and control group. The mortality rate, myocardial histopathology changes, heart to body weight (HW/BW) ratio and serum myocardial enzyme were examined. Results The mortality rate in high dosage group was significantly higher than that of other groups (100.0%, 55.0%, 10.0% and 0, respectively).The myocardial lesions, HW/BW ratio and serum myocardial enzyme at d7 in the high dosage group were significantly higher than those of other groups. The middle dosage group showed a significantly increased myocardial lesions, HW/BW ratio and serum myocardial enzyme compared with the lower dosage group. Conclusion The 10^3TCID50 inoculation concentration is suggested to establish the murine myocarditis model.
出处 《浙江医学》 CAS 2007年第11期1166-1168,共3页 Zhejiang Medical Journal
关键词 柯萨奇病毒B组 接种浓度 心肌炎模型 病毒浓度 Coxsackievirus B Inoculation concentration Myocarditis model Virus concentration
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  • 1Zaidi S H, Hui C C, Cheah A Y, et al. Targeted overexpression of elafin protects mice against cardiac dysfunction and mortality following viral myocarditis [J]. J Clin Invest, 1999, 103 (8): 1211- 1219.
  • 2Lewis D A, Dhala A. Syncope in the pediatric patient. The cardiologist's perspective[J]. Pediatr Clin North Am, 1999, 46 (2): 205-219.
  • 3刘晶星,陆德源,沈鼎鸿,陈曙霞,郑新娟,常佩伦,姚季生,姚申.病毒性心肌炎致病机理的实验研究——组织病理和心电图观察[J].上海第二医科大学学报,1990,10(1):16-22. 被引量:18
  • 4Badorff C, Lee G H, I,amphear B J, et al. Enteroviral protease 2A cleaves dystrophin:evidenee of cytoskeletal disruption in an acquired cardiomyopathy[J]. Nat Med, 1999, 5 (3): 320-326.
  • 5Petersen J F W, Cherney M M, Liebig H D, et al. The structure of the 2A proteinase from a common cold virus:a proteinase responsible for the shut-off of host-cell protein syntesis[J]. EMBO, 1999, 18(20): 5463-5475.
  • 6Martin R, Bennett. Apoptosis in the cardiovascular system[J]. Heart, 2002, 87(5): 480-487.
  • 7Horwitz M S, La-Cava A, Fine C, et al. Pancreatic expression of interferon-gamma protects mice from lethal coxsackievirus B3 infection and subsequent myocarditis [J]. Nat Med, 2000, 6 (6): 693-697.
  • 8Matsumori A. Cytokines in myocarditis and dilated cardiomyopathy [J]. Eur Heart J, 2002, 4(1): 142-145.
  • 9Wada H, Saito K, Kanda T, et al. Tumor necrosis factor-alpha (TNF-alpha) plays a protective role in acute viral myocarditis in mice-A study using mice lacking TNF-alpha[J]. Circulation, 2001, 103(5): 743-749.

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