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免疫抑制小鼠模型中生物发光诱导的肺部感染的成像

Imaging of bioluminescent induced pulmonary infection in an immunosuppressed mouse model.

作者信息

Hu Xing, Cai Yun, Wang Yuhang, Wang Rui, Wang Jin, Zhang Bo

机构信息

Medical School of Chinese PLA, Beijing, China.

Department of Pharmacy, Centre of Medicine Clinical Research, PLA General Hospital, Beijing, China.

出版信息

J Int Med Res. 2020 Oct;48(10):300060520956473. doi: 10.1177/0300060520956473.

Abstract

OBJECTIVE

To establish a mouse model of bioluminescent -induced lung infection, under different infection states after pretreatment with various dosages of cyclophosphamide (CTX).

METHODS

A strain carrying the operon was used to infect immunocompetent mice (intraperitoneal injection of saline at 4 days and 1 day prior to experimental lung infection) and immunodeficient mice (50 mg/kg CTX at 4 days and 50 mg/kg CTX at 1 day prior to lung infection; or 150 mg/kg CTX at 4 days and 100 mg/kg CTX at 1 day prior to lung infection). Disease progression was monitored in living mice using a bioluminescence imaging system. The bioluminescent images, bacterial loads in lungs, blood cytological changes and histopathology of lungs were analysed.

RESULTS

-induced lung infection models were established in mice pretreated with CTX. Different doses of CTX led to different severities of lung infection. Mice pretreated with 150/100 mg/kg CTX were more suitable for real-time monitoring as they had more typical bioluminescent images of lung infection, more obvious changes in the bioluminescent intensity values, more bacterial colonies in the lungs and more distinct pulmonary pathological changes.

CONCLUSIONS

A stable bioluminescent -induced lung infection model was successfully established in mice pretreated with CTX, which can be semi-quantitatively monitored in real-time.

摘要

目的

建立环磷酰胺(CTX)不同剂量预处理后处于不同感染状态的生物发光诱导肺部感染小鼠模型。

方法

使用携带操纵子的菌株感染免疫健全小鼠(在实验性肺部感染前4天和1天腹腔注射生理盐水)和免疫缺陷小鼠(肺部感染前4天给予50 mg/kg CTX,肺部感染前1天给予50 mg/kg CTX;或肺部感染前4天给予150 mg/kg CTX,肺部感染前1天给予100 mg/kg CTX)。使用生物发光成像系统监测活体小鼠的疾病进展。分析生物发光图像、肺部细菌载量、血液细胞学变化和肺部组织病理学。

结果

在CTX预处理的小鼠中建立了诱导肺部感染模型。不同剂量的CTX导致不同严重程度的肺部感染。用150/100 mg/kg CTX预处理的小鼠更适合实时监测,因为它们具有更典型的肺部感染生物发光图像、生物发光强度值变化更明显、肺部细菌菌落更多以及肺部病理变化更明显。

结论

在CTX预处理的小鼠中成功建立了稳定的生物发光诱导肺部感染模型,可进行实时半定量监测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d75/7556177/74f1f01c84e7/10.1177_0300060520956473-fig1.jpg

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