检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:陈盛霞[1] 陈家旭[1] 徐会娟[1] 马和祥[1] 帅连云[1] 仇锦波[1] 唐学恒[2]
机构地区:[1]江苏大学医学检验系,镇江212001 [2]苏州大学基础医学系
出 处:《中国人兽共患病杂志》2002年第1期79-81,共3页Chinese Journal of Zoonoses
基 金:江苏省教育厅自然科学基金项目 (NO :0 0KJB310 0 0 9)
摘 要:目的 比较用SpragueDawley(SD)大鼠和Wistar大鼠建立卡氏肺孢子虫肺炎 (PCP)模型的差异。 方法 选用SD大鼠和Wistar大鼠 ,随机分为实验组和对照组 ,免疫抑制诱导建立动物模型 ;收集肺组织和支气管肺泡灌洗液 (BALF) ,分别制成肺印片和BALF涂片 ,作Giemsa染色 ,镜检卡氏肺孢子虫滋养体和包囊。结果 共收集实验组SD大鼠和Wistar大鼠的肺组织及BALF标本各 2 8份 ,经Giemsa染色后 ,在肺印片中查见Pneumocystiscarinii(Pc)虫体的阳性率分别为 89.2 9%和10 0 % ,两者之间无显著性差异 (P >0 .0 5 ) ;BALF阳性率分别为 6 0 .71%和 78.5 7% ,两者之间亦无显著性差异 (P >0 .0 5 )。而同种大鼠的肺印片与BALF涂片 ,其阳性率之间有显著性差异 (P <0 .0 5 ) ,且肺印片的检出率均显著高于BALF涂片。同种大鼠不同肺叶的肺印片 ,其阳性率之间无显著性差异 (P >0 .0 5 )。Aim To compare Sprague Dawley(SD) rats with Wistar rats in rat model of Pneumocystis carinii pneumonia.Methods SD and Wistar rats were divided into experimental group and control group randomly,and were induced by immunosuppression.Lung tissues and bronchoalveolar lavage fluid (BALF) were collected.Smears were made from lung tissues and BALF sediments,were stained by Giemsa,and were examined for identifying the cysts and trophozoits of P.carinii.Results 28 samples were collected in the experimental group in lung tissues and BALF respectively.The positive rates of P.carinii organisms were 89.29% and 100% in lung smears,and were 60.71% and 78.57% in BALF slides,respectively.The difference between the SD and Wistar rats was no significant (P>0.05).The positive rates in lung smears were higher than that of BALF slides and the difference between the two methods was significant (P<0.05).The positive rates in lung smears from different lobes were no significant (P>0.05).Conclusions SD and Wistar rats had no significant difference in animal model of P.carinii.
关 键 词:大鼠 卡氏肺孢子虫 卡氏肺孢子虫肺炎 模型 GIEMSA染色
分 类 号:R382.3[医药卫生—医学寄生虫学]
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.74