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作 者:封继宏[1] 祁海燕[2] 郑兆晔[1] 刘伟[1] 苏景深[1] 关鹏[1] 杨爽[2] 李云辉[2] 李美凤[1] 孙增涛[1]
机构地区:[1]天津中医药大学第二附属医院,天津300150 [2]天津中医药大学,天津300193
出 处:《辽宁中医药大学学报》2015年第11期68-70,共3页Journal of Liaoning University of Traditional Chinese Medicine
基 金:国家自然科学基金资助项目(81202796)
摘 要:目的:寻求一种在损伤最小的情况下建立慢性阻塞性肺病急性加重期(AECOPD)大鼠模型的新方法。方法:将40只大鼠分为正常对照组、模型组,乙醚麻醉后,在硬式鼻腔镜引导及松下摄录监视系统下,使用自制鼠麻醉喉镜,气管内隔周定期注入弹性蛋白酶,并最后滴入细菌,从而建立AECOPD大鼠模型。结果:模型组大鼠精神萎靡,动则气喘,呼吸深大,气道分泌物增多;肺组织体积增大、出现瘀血,病理结果显示肺泡壁变薄变大,肺泡腔融合增大,部分破裂融合形成肺大泡,肺泡数目明显减少,肺泡周围可见炎细胞浸润,改变与人类COPD改变相符合。模型组大鼠肺功能FEV0.3、FEV0.3/FVC、FVC较正常对照组显著下降。结论:通过运用硬式鼻腔镜、松下摄录监视系统及自制鼠麻醉喉镜,气管内滴入弹性蛋白酶,并结合细菌攻击可以成功建立AECOPD大鼠模型。Objective:To find a new way for the establishment of chronic obstructive pulmonary disease with acute exacerbation(AECOPD) in rats with minimal damage. Methods:40 rats were divided into normal control group and medel group. After anesthetized,drop elastase with the help of rigid nasal mirror and homemade laryngoscope every other week on a regular basis,finally drop bacterial to establish rats models of AECOPD. Results:The model group:listlessness,out of breath after moving,deep breath,increased airway secretions,lung volume increases,congestion. Pathology showed:alveolar wall become thinner and larger,alveolar fusion increases,broken parts form bulla,the number of alveolar reduced,inflammatory cell infiltration were seen around. It is consistent with human COPD.Lung function of FEV0.3,FEV0.3/FVC and FVC was significantly decreased in model group,compared with the control group. Conclusion:Animal model of AECOPD can be successfully established by drop elastase and Bacterial,with the rigid nasal mirror and homemade laryngoscope.
关 键 词:慢性阻塞性肺疾病急性加重 动物模型 硬式鼻腔镜 弹性蛋白酶 细菌
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