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两种大鼠哮喘模型建立方法的比较    

Comparison of Two Methods to Establish Rat Models of Asthma

文献类型:期刊文献

中文题名:两种大鼠哮喘模型建立方法的比较

英文题名:Comparison of Two Methods to Establish Rat Models of Asthma

作者:劳文艳[1,2];阮研硕[3];周艳丽[1];陈世杰[1];赵晓红[1,2]

第一作者:劳文艳

机构:[1]北京联合大学功能食品科学技术研究院;[2]北京联合大学生物活性物质与功能食品北京市重点实验室;[3]中国医学科学院医学实验动物研究所

第一机构:北京联合大学生物化学工程学院功能食品科学技术研究院|北京联合大学应用文理学院

年份:2017

卷号:31

期号:3

起止页码:54-58

中文期刊名:北京联合大学学报

外文期刊名:Journal of Beijing Union University

语种:中文

中文关键词:哮喘;炎性反应;卵清蛋白特异性Ig;E

外文关键词:Asthma; Inflammation ; OVA-IgE

摘要:以两种方法建立哮喘大鼠模型,方法一:用新鲜配制的卵清蛋白(OVA)(0.2 mg)致敏,氢氧化铝作为佐剂,连续7天进行1%OVA雾化激发,30 min/次;方法二:用高剂量卵清蛋白(2 mg)致敏,氢氧化铝(Al(OH)_3)与百日咳灭活杆菌共同作为佐剂,先以1.7%OVA气管滴注染毒,随后1%OVA连续雾化激发6 d,30 min/次。通过肺组织形态学观察、无创肺功能测试、肺泡灌洗液(BALF)中炎性细胞分类及计数、组织样本中特异性蛋白IgE以及卵清蛋白特异性IgE(OVA-IgE)含量作为敏感指标判断哮喘模型建立成功与否。结果显示两种哮喘模型大鼠均表现出哮喘大鼠的肺组织病理学改变,肺功能降低,BALF中的细胞总数、淋巴细胞、嗜酸性粒细胞数增加;采用方法二能够引起组织样本中IgE以及OVA-IgE含量增高,而采用造模方法一未观察到此类变化。因此,方法二能够更好地制备过敏性哮喘模型,可作为较好的哮喘大鼠模型建立方法。
Rats allergic asthma models were estabalished in two different ways. The first one was sensitized with ovatbumin (OVA) (0.2 mg) freshly prepared, A1 (OH)3 used as an adjuvant and 1% OVA atomized for seven days, 30 minutes a time; The second one was sensitized by high dose ovalbumin (2 mg), AI(OH)3 used as an adjuvant with Bordetella pertussis, and first exposed by 1.7% OVA instillation, followed by 1% OVA continuous nebulization for 6 days, 30 minutes a time. To determine whether the asthma model is successful or not, the tistopathological changes of lung tissue and noninvasive pulmonary function were detected; bronchoalveolar lavage fluid (BALF) was collected to count the number of inflammatory cells; the homogenate supernatant of lung tissue was collected for detecting the concentrations of immunoglobulin E (IgE) and Ovalbumin immunoglobulin E (OVA-IgE). The results showed that, in the two asthmatic rats, the lung tissue pathological was changed; the lung function were decreased; the total number of ceils and the number of lymphocytes and eosinophils in BALF were increased. The second method could increase the content of IgE and OVA-IgE in lung tissue, but the first one was not observed. So the second method to make asthma model is better, thus it could be choosen in the following studies.

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