期刊文献+

大鼠结核性胸膜炎模型及其胸膜的病理学与超微病理学观察

Pleural pathological and ultrastructural pathology features in the model of tuberculous pleurisy in rats
下载PDF
导出
摘要 目的证实结核性胸膜炎大鼠模型的建立方法;观察大鼠结核性胸膜炎的胸膜组织形态及超微结构特征,进一步探讨结核性胸膜炎的发病过程及胸液渗出与吸收不平衡的原因。方法健康雌性Wistar大鼠30只,随机分成2组,对照组6只,模型组24只,复制结核性胸膜炎动物模型;分别于建模后2、4、6、8、10、12、14、16、18、22、26及30d处死。观察大鼠胸腔内积液特征及胸膜结构变化,并进行病理学及超微病理学观察。结果模型组24只大鼠成功复制出结核性胸膜炎模型,形成胸腔积液及胸膜结核结节,后期胸膜肥厚粘连。透射电镜观察显示,早期间皮细胞微绒毛减少,细胞膜、细胞质、细胞器损伤,中期间皮细胞逐渐消失,纤维细胞与成纤维细胞增生,后期由增生的胶原纤维替代原有胸膜结构。结论接种卡介苗5周后向大鼠胸膜腔内注入标准人型结核菌株H37RV结核分枝杆菌悬液,可以建立结核性胸膜炎的动物模型。胸膜间皮细胞的损伤及丢失,影响了胸水的回吸收。胸膜类上皮细胞肉芽肿及纤维组织的增生可能导致淋巴管阻塞,减少了胸水的渗出,同时可能破坏了间皮细胞与淋巴孔之间形成的回吸收通路。 【Objective】To develop a rat model of tuberculosis pleurisy and to identify the rat tuberculosis pleurisy histo-structure and ultra-structure of different stages in order to identify the reason of chest fluid unbalanced effusion and absorption.【Methods】30 healthy female Wistar rats randomly divided into two groups,control group 6 rats,model group 24 rats,copy a rat model of tuberculosis pleurisy;sacrificed in different stage.The model group rats were killed in group on days 2,4,6,8,10,12,14,16,18,22,26 and 30.To observe the characters of the chest fluid and the change of the pleura structure,and observe the change of the pathology and ultra-pathology.【Results】To succeed copying the rat model of tuberculosis pleurisy in model group and to form chest fluid,tubercler and pachynsis pleurae.There were decreased of microvillus from mesothelial cell,damaged of cellular membrane,cytoplasm and cell organ,to reach the diminish of mesothelial cell,proliferation of fibrocyte and fibroblast,and proliferation of collagen fibers.【Conclusion】After injected BCG 5 weeks,injected tuberculosis bacilli H37RV suspension could establish a rat model of tuberculosis pleurisy.The damage of pleura mesothelial cell effects the absorb of chest fluid.The pleura epithelioid cell granuloma and the proliferation of fibrous tissue may block the lymph vessels,decrease the effusion of the chest fluid,and may damage the absorb way between the mesothelial cell and the ostium lymphaticum.
出处 《中国现代医学杂志》 CAS CSCD 北大核心 2009年第24期3721-3725,3730,共6页 China Journal of Modern Medicine
关键词 结核 胸膜炎 病理学 超微病理学 tuberculosis pleurisy pathological ultrastructural pathology
  • 相关文献

参考文献2

二级参考文献15

  • 1朱愉 多秀瀛.实验动物的疾病模型[M].天津:天津科技翻译出版公司,1999.549-551.
  • 2Youmans G P 张天民(译).结核病学[M].中华医学湖北分会,1983.219-232.
  • 3卢润生 漆浩珊 等.结核菌实验动物探讨[J].中国防痨通讯,1990,12(3):118-119.
  • 4Antomy VB, Repine JB, Harada RV, et al. Inflammatory responses in experimental tuberculosis pleurisy. Acta Cytologica, 1983, 27:355 -361.
  • 5Serbina N, Flynn J. Early emergence of CD8^+ T cells primed forproduction of type 1 cytokines in the lungs of mycobacterium tuberculosis -infected mice. Infect Immun,1999, 67:3980-3988.
  • 6Tumer J, Corrah T, Sabbally S,et al. A longitudinal study of in vitro IFN-γ production and cytotoxic T cell responses of tuberculosis patients in the Gambia. Tuber Lung Dis ,2000,80 : 161-169.
  • 7Hussain R, Kaleem A, Shahid F, et al. Cytokine profiles using whole-blood assays can discriminate between tuberculosis patients and healthy endemic controls in a BCG-vaccinated population. J Immunol Methods, 2002, 264:95-108.
  • 8Marisol HG, Patricia MS. Transforming growth factor-β1 decreases survival of mycobacterium bovis-activated T cells. Arch Med Res,2003,34:20-25.
  • 9Aoe K, Hiraki A, Murakami T, et al. Diagnostic significance of interferon-gamma in tuberculous pleural effusions. Chest,2003,123 :740 -744.
  • 10Melis M, Pace E, Siena L, et al. Biologically active intercellular adhesion molecule-1 in shed as dimers by a regulated mechanism in the inflamed pleural space. Am J Respir Care Med, 2003, 167:1131-1138.

共引文献24

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