CAJ | 학술논문

目的建立小鼠侵袭性肺曲霉菌病（IPA）的动物模型。方法将90只小鼠随机分为5组，模型组：于接种前4天和接种前1天腹腔注射环磷酰胺200 mg/kg，通过鼻腔吸入浓度为1×1011/L烟曲霉菌孢子悬液40μl。非环磷酰胺对照组：除以0.9%氯化钠注射液（NS）代替环磷酰胺外，其余操作同模型组。环磷酰胺对照组：以NS代替烟曲霉菌滴鼻，其余操作同模型组。空白对照组：用NS代替环磷酰胺行腹腔注射，以NS代替烟曲霉菌孢子，其余操作同模型组。重组人粒细胞集落刺激因子（G-CSF）组：在模型组基础上，接种真菌孢子1天后皮下注射G-CSF 20μg?kg-1?d-1。通过肺组织病理、肺组织真菌培养和血清半乳甘露聚糖测定（GM试验）等确定肺侵袭性曲霉菌病模型是否构建成功。结果肺曲霉菌培养、血清GM试验和病理切片等结果均表明，模型组和G-CSF组均发生了IPA，其余各组均无IPA发生。结论成功建立了小鼠肺曲霉菌模型。
목적건립소서침습성폐곡매균병（IPA）적동물모형。방법장90지소서수궤분위5조，모형조：우접충전4천화접충전1천복강주사배린선알200 mg/kg，통과비강흡입농도위1×1011/L연곡매균포자현액40μl。비배린선알대조조：제이0.9%록화납주사액（NS）대체배린선알외，기여조작동모형조。배린선알대조조：이NS대체연곡매균적비，기여조작동모형조。공백대조조：용NS대체배린선알행복강주사，이NS대체연곡매균포자，기여조작동모형조。중조인립세포집락자격인자（G-CSF）조：재모형조기출상，접충진균포자1천후피하주사G-CSF 20μg?kg-1?d-1。통과폐조직병리、폐조직진균배양화혈청반유감로취당측정（GM시험）등학정폐침습성곡매균병모형시부구건성공。결과폐곡매균배양、혈청GM시험화병리절편등결과균표명，모형조화G-CSF조균발생료IPA，기여각조균무IPA발생。결론성공건립료소서폐곡매균모형。
Objictive To establish a model of invasive pulmonary aspergillosis (IPA) in mouse. Mehtods Total of 90 mouse were divided into 5 groups randomly. Mouse in model group received cyclophosphamide (intraperitoneal 200 mg/kg, 4 th day and 1 st day before inoculation) and aspergillus A. fumigatus conidia suspension (intranasal 40 μl/mice, 1 × 1011/L). Mouse in non-immunosuppressant control group received normal saline instead of cyclophosphamide and other procedures were the same as the model group. Mouse in immunosuppressant control group received normal saline instead of A. fumigatus conidia suspension and other procedures were the same as the model group. Mouse in normal saline control group received normal saline instead of cyclophosphamide and normal saline instead of A. fumigatus conidia suspension. Mouse in G-CSF group were given at dose of 20 μg?kg-1?d-1 from 1st day and other procedures were the same as the model group. Pathologic examination, culture of the lungs of mice and GM-test were conducted to determine whether the IPA model was successfully establish. Results IPA was conifrmed in all mice in the model group and the G-CSF group 5 days after inoculation of A. fumigatus conidia based on pathologic examination and culture of lung tissue and GM-test. No-IPA was found in the non-immunosuppressant control group, the immunosuppressant control group and the normal saline control group. Conclusions The IPA model in mouse was successfully constructrued.