中华微生物学和免疫学杂志
中華微生物學和免疫學雜誌
중화미생물학화면역학잡지
CHINESE JOURNAL OF MICROBIOLOGY AND IMMUNOLOGY
2010年
8期
717-721
,共5页
于柏峰%谷海瀛%翟英超%赵振东%袁素
于柏峰%穀海瀛%翟英超%趙振東%袁素
우백봉%곡해영%적영초%조진동%원소
动物模型%铜绿假单胞菌%肺部感染%炎症反应
動物模型%銅綠假單胞菌%肺部感染%炎癥反應
동물모형%동록가단포균%폐부감염%염증반응
Animal model%Pseudomonas aeruginosa%Pulmonary infection%Inflammation
目的 为了对铜绿假单胞菌引起的慢性呼吸道感染性疾病的研究,需要真实客观地反映在体内环境综合影响下该菌的致病情况,为此建立了慢性铜绿假单胞菌的肺炎动物模型,并对其引起的相关炎症反应进行分析.方法 用富含铜绿假单胞菌的琼脂糖珠灌注小鼠,建立铜绿假单胞慢性感染的动物模型,通过检测肺泡灌注液(BALF)中白细胞数、中性粒细胞百分比、白细胞介素,血清中核基质蛋白MMP-2浓度及肺组织的病理切片观测其炎症反应情况.结果 感染后动物模型肺部检出铜绿假单胞菌并出现病理改变,肺部感染各项炎症指标在2~3 d达到峰值,大致7 d恢复正常;铜绿假单胞菌肺炎模型小鼠循环系统中检测MMP-2升高,说明该炎症反应在一定程度上可引起肺部纤维化.结论 本实验成功建立了慢性铜绿假单胞菌的肺炎动物模型,可在此基础上对该菌的致病性及耐药性进行进一步研究.
目的 為瞭對銅綠假單胞菌引起的慢性呼吸道感染性疾病的研究,需要真實客觀地反映在體內環境綜閤影響下該菌的緻病情況,為此建立瞭慢性銅綠假單胞菌的肺炎動物模型,併對其引起的相關炎癥反應進行分析.方法 用富含銅綠假單胞菌的瓊脂糖珠灌註小鼠,建立銅綠假單胞慢性感染的動物模型,通過檢測肺泡灌註液(BALF)中白細胞數、中性粒細胞百分比、白細胞介素,血清中覈基質蛋白MMP-2濃度及肺組織的病理切片觀測其炎癥反應情況.結果 感染後動物模型肺部檢齣銅綠假單胞菌併齣現病理改變,肺部感染各項炎癥指標在2~3 d達到峰值,大緻7 d恢複正常;銅綠假單胞菌肺炎模型小鼠循環繫統中檢測MMP-2升高,說明該炎癥反應在一定程度上可引起肺部纖維化.結論 本實驗成功建立瞭慢性銅綠假單胞菌的肺炎動物模型,可在此基礎上對該菌的緻病性及耐藥性進行進一步研究.
목적 위료대동록가단포균인기적만성호흡도감염성질병적연구,수요진실객관지반영재체내배경종합영향하해균적치병정황,위차건립료만성동록가단포균적폐염동물모형,병대기인기적상관염증반응진행분석.방법 용부함동록가단포균적경지당주관주소서,건립동록가단포만성감염적동물모형,통과검측폐포관주액(BALF)중백세포수、중성립세포백분비、백세포개소,혈청중핵기질단백MMP-2농도급폐조직적병리절편관측기염증반응정황.결과 감염후동물모형폐부검출동록가단포균병출현병리개변,폐부감염각항염증지표재2~3 d체도봉치,대치7 d회복정상;동록가단포균폐염모형소서순배계통중검측MMP-2승고,설명해염증반응재일정정도상가인기폐부섬유화.결론 본실험성공건립료만성동록가단포균적폐염동물모형,가재차기출상대해균적치병성급내약성진행진일보연구.
Objective To research the chronic respiratory infectious diseases caused by Pseudomonas aeruginosa need to objectively the reflection of the real environment in the body, so established a mouse model of chronic pulmonary infection with Pseudomonas aeruginosa and analyzed it's inflammatory response. Methods Establishment of chronic bronchial infection mice model that were inoculated with Pseudomonos aeruginosa-laden agarose beads, and analyzed its inflammatory response by detected the cytokines and MMP-2, and a differential cell count and a total leukocytes count were performed as well. Results Pseudomonas aeruginosa had been detected after infection, and there were changes in pathological. Pulmonary inflammation appeared in 1 d and reached near baseline levels by 7 d after inoculation. It was verified that the peak of inflammatory reaction in Pseudomonas aeruginosa infection is in 2-3 d; the mice did have detectable levels of circulating matrix metalloproteinase-2 ( MMP-2 ) after infection with Pseudomonas aeruginosa. MMP-2 concentrations in the blood serum peaked at 3 d after inoculation. It is indicated that Pseudomonas aeruginosa can initiate a certain degree of pulmonary fibrosis on the basis of the pulmonary inflammation. Conclusion In this study, chronic bronchial infection animal model affected by Pseudomonas aeruginosa was established successfully. Base on this animal model, we can do the pathogenicity and drug resistance of Pseudomonas aeruginosa further study.