Huang Xiao-Hong, Gong Ming, Li Tao, Jiang Wen-Ling, Liu Jing, Yang Zhan-Qiu
Department of Pharmacy, Guangdong Provincial People's Hospital, Guangzhou 510080, China.
Nan Fang Yi Ke Da Xue Xue Bao. 2009 Nov;29(11):2219-21.
To establish a rat model of mycoplasma pneumonia (MP) for investigating the pathogenesis of MP and its therapy with drugs.
Thirty Wistar rats were randomly divided into 6 groups (n=5), including a control group, a MP model group, a erythromycin lactobionate group and 3 erythromycin microspheres groups (high, middle, and low dose groups). With the exception of those in the control group, all the rats received intranasal MP administration followed by corresponding treatments administered via tail vein injection. At different time points after inoculation of the pathogen, the lungs of the rats were taken for histopathological scoring.
In the MP model group, the lung pathology was characterized by patchy interstitial pneumonitis with predominantly lymphocyte infiltration and mucosal edema. The bronchiolar walls became thickened and the lumens narrowed. In erythromycin lactobionate and erythromycin microspheres treatment (high and middle dose) groups, clear cell boundaries were observed in the lungs where no obvious pathological changes were found. RT-PCR amplification showed positive results of MP RNA in the model group, erythromycin lactobionate group and erythromycin microsphere groups.
The approach described is practicable to establish rat models of MP. Erythromycin microspheres can effectively relieve the lung inflammations and has therapeutic effect on MP.
建立支原体肺炎(MP)大鼠模型,以研究MP的发病机制及其药物治疗。
将30只Wistar大鼠随机分为6组(n = 5),包括对照组、MP模型组、乳糖酸红霉素组和3个红霉素微球组(高、中、低剂量组)。除对照组外,所有大鼠均经鼻内给予MP,随后通过尾静脉注射给予相应治疗。在接种病原体后的不同时间点,取大鼠肺组织进行组织病理学评分。
MP模型组肺病理表现为斑片状间质性肺炎,以淋巴细胞浸润为主,伴有黏膜水肿。细支气管壁增厚,管腔狭窄。在乳糖酸红霉素和红霉素微球治疗(高、中剂量)组中,肺组织细胞边界清晰,未见明显病理改变。RT-PCR扩增显示模型组、乳糖酸红霉素组和红霉素微球组MP RNA呈阳性结果。
所描述的方法可用于建立MP大鼠模型。红霉素微球可有效减轻肺部炎症,对MP有治疗作用。