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1. 首都医科大学附属北京友谊医院药学部
2. 首都医科大学附属北京友谊医院检验科
纸质出版日期:2021,
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马致洁, 吕治, 于小红, 等. 生姜泻心汤对感染难辨梭菌小鼠的治疗作用研究[J]. 中国医院用药评价与分析, 2021,21(11):1281-1285.
MA Zhijie, LYU Zhi, YU Xiaohong, et al. Therapeutic Effects of Shengjiang Xiexin Decoction on Mice Infected with Clostridium Difficile[J]. 2021,21(11):1281-1285.
马致洁, 吕治, 于小红, 等. 生姜泻心汤对感染难辨梭菌小鼠的治疗作用研究[J]. 中国医院用药评价与分析, 2021,21(11):1281-1285. DOI: 10.14009/j.issn.1672-2124.2021.11.001.
MA Zhijie, LYU Zhi, YU Xiaohong, et al. Therapeutic Effects of Shengjiang Xiexin Decoction on Mice Infected with Clostridium Difficile[J]. 2021,21(11):1281-1285. DOI: 10.14009/j.issn.1672-2124.2021.11.001.
目的:探讨生姜泻心汤对感染难辨梭菌小鼠的治疗作用。方法:采用C57BL/6小鼠难辨梭菌感染模型
将小鼠分为正常组、模型组、万古霉素组(50 mg/kg)和万古霉素联合生姜泻心汤低剂量组(万古霉素50 mg/kg+生姜泻心汤16.4 g/kg)
以及生姜泻心汤低剂量组(16.4 g/kg)、高剂量组(32.8 g/kg)
所有小鼠连续给药7 d。通过体重、艰难梭菌毒素A&B水平和肠组织病理苏木精-伊红染色情况等评价生姜泻心汤治疗难辨梭菌感染的疗效。结果:造模前至造模成功时
各组小鼠体重稳步升高;造模成功后至治疗中期
小鼠体重持续降低
其中模型组降低最明显;治疗期
除生姜泻心汤高剂量组小鼠在治疗第5日的体重低于模型组
其他监测时间点
模型组小鼠体重显著低于万古霉素组、万古霉素联合生姜泻心汤低剂量组和生姜泻心汤低剂量组
差异均有统计学意义(P <0.05);观察期
各组小鼠体重仍持续升高。万古霉素组、万古霉素联合生姜泻心汤低剂量组小鼠的难辨梭菌毒素A&B水平得到有效降低
与模型组相比
差异有统计学意义(P <0.01/0.05);停药观察第5日
难辨梭菌毒素A&B水平较观察第2日升高
与模型组的差异均无统计学意义(P> 0.05)。生姜泻心汤低剂量组小鼠治疗3 d后的艰难梭菌毒素A&B水平降至正常水平
与模型组相比
差异有统计学意义(P <0.01/0.05)
且该水平维持至停药观察5 d。肠组织病理苏木精-伊红染色结果显示
治疗后
除生姜泻心汤高剂量组小鼠肠组织局部黏膜下层可见少量淋巴细胞浸润外
其他各组均未见肠组织有明显损伤。结论:生姜泻心汤单独使用的抑菌能力虽不及万古霉素
但仍表现出了一定的治疗作用;与万古霉素单独使用相比
生姜泻心汤低剂量联合万古霉素对毒素水平的抑制能力较稳定。生姜泻心汤的治疗作用稳定
起效较慢
且无复发迹象
体现了中药多成分、多靶点的作用特点和优势
为临床难辨梭菌感染提供了一种新的治疗策略参考。
OBJECTIVE: To probe into the therapeutic effect of Shengjiang Xiexin decoction on mice infected with Clostridium difficile( C. difficile). METHODS: The C57 BL/6 mice infected with C. difficile were divided into the normal group
model group
vancomycin group( 50 mg/kg)
vancomycin combined with Shengjiang Xiexin decoction low-dose group( vancomycin 50 mg/kg + Shengjiang Xiexin decoction 16. 4 g/kg)
and Shengjiang Xiexin decoction low-dose group( 16. 4 g/kg) and high-dose group( 32. 8 g/kg). All mice were dosed continuously for 7 d. The efficacy of Shengjiang Xiexin decoction in the treatment of C. difficile. infection was evaluated based on the mortality
body weight
A&B level of C. difficile
and HE staining of intestinal histology. RESULTS: The body weight of mice in each group increased steadily from before modeling to the time of successful modeling; after successful modeling to the middle of treatment
the body weight of mice continued to decrease
with the most obvious decrease in the model group.During the treatment
the body weight of mice in the model group was significantly lower than that in the vancomycin group
the vancomycin combined with Shengjiang Xiexin decoction low-dose group
and the Shengjiang Xiexin decoction low-dose group at other monitoring time points
with statistically significant difference( P < 0. 05)
except for the body weight of mice in the Shengjiang Xiexin decoction high-dose group was lower than that in the model group on the 5 th day of treatment. During the observation period
the body weight of mice in each group continued to increase.Compared with the model group
the A&B level of C. difficile decreased effectively in the vancomycin group and the vancomycin combined with Shengjiang Xiexin decoction low-dose treatment group( P < 0. 01/0. 05). On the 5 th day of drug withdrawal
the A&B level of C. difficile increased compared with the 2 nd day of observation in the vancomycin group and the vancomycin combined with Shengjiang Xiexin decoction low-dose treatment group
and there was no statistical significance compared with the model group( P > 0. 05). After 3 d of treatment
the A&B level of C. difficile in the Shengjiang Xiexin decoction low-dose group decreased to the normal level
and the difference was statistically significant compared with that in the model group( P < 0. 01/0. 05)
and the level was maintained until the drug withdrawal for 5 d. HE staining results of intestinal tissue pathology showed that after treatment
no obvious intestinal tissue damage was observed in other groups except fro a small amount of lymphocyte infiltration in the local submucosa of the mice in the Shengjiang Xiexin decoction high-dose group. CONCLUSIONS: Although Shengjiang Xiexin decoction alone is not as strong as vancomycin in antibacterial activity
it still shows a certain therapeutic effect; compared with vancomycin alone
the inhibition ability on toxin level in Shengjiang Xiexin decoction high-dose group combined with vancomycin group is relatively stable. Shengjiang Xiexin decoction has the stable therapeutic effect
slow onset and no signs of recurrence
which reflects the characteristics and advantages of multi-component and multi-targeted traditional Chinese medicine
and provides the new treatment strategy reference for clinical C. difficile infection.
生姜泻心汤艰难梭菌感染C57BL/6小鼠
Shengjiang Xiexin decoctionClostridium difficile infectionC57BL/6 mice
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