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1.北京中医药大学中医学院糖尿病研究中心 北京 100029
2.北京开放大学城市管理学院
3.北京中医药大学第三附属医院
4.北京中医药大学信息与教育技术中心
ZHAO Dandan, Ph. D., Associate Researcher, Master’s Supervisor. Diabetes Research Center, School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, No.11, Beisanhuan Donglu Road, Chaoyang District, Beijing 100029. E-mail: bucmzhaodandan@163.com
Received:19 May 2023,
Published Online:12 September 2023,
Published:30 November 2023
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YE Zimengwei, XU Bingrui, ZHAO Yi, et al. Effect of ginsenoside Rb1, berberine, and their combination on intestinal flora in obese mice[J]. Journal of beijing university of traditional chinese medicine, 2023, 46(11): 1541-1553.
YE Zimengwei, XU Bingrui, ZHAO Yi, et al. Effect of ginsenoside Rb1, berberine, and their combination on intestinal flora in obese mice[J]. Journal of beijing university of traditional chinese medicine, 2023, 46(11): 1541-1553. DOI: 10.3969/j.issn.1006-2157.2023.11.009.
目的
2
探讨人参皂苷Rb
1
、小檗碱及其联合应用对高脂饮食诱导肥胖小鼠肠道菌群的影响。
方法
2
42只SPF级雄性C57BL/6J小鼠高脂饲料喂养12周建立肥胖小鼠模型。将符合肥胖标准的32只肥胖小鼠任意分为4组:对照组、人参皂苷Rb
1
组(20 mg/kg)、小檗碱组(50 mg/kg)、人参皂苷Rb
1
+小檗碱组(人参皂苷Rb
1
20 mg/kg +小檗碱50 mg/kg),每组8只。连续灌胃给药8周,给药期间小鼠继续给予高脂饲料喂养。每周记录各组小鼠的体质量,每2周检测小鼠空腹血糖。实验结束后留取粪便,进行16 S rDNA测序,观察各组小鼠肠道菌群变化。
结果
2
与对照组比较,人参皂苷Rb
1
组、小檗碱组和人参皂苷Rb
1
+小檗碱组第4~6周小鼠体质量降低,第4、6、8周小鼠空腹血糖降低(均
P
<
0.05)。人参皂苷Rb
1
组、小檗碱组和人参皂苷Rb
1
+小檗碱组高脂饮食诱导的肠道生态失调均改善,拟杆菌门/厚壁菌门值增加,脱铁杆菌门、小螺菌属、螺杆菌属、多尔菌属、瘤胃球菌属和臭气杆菌属等有害菌群的相对丰度降低。
结论
2
人参皂苷Rb
1
、小檗碱及其联合应用可降低高脂饮食诱导的肥胖小鼠体质量,作用机制可能与其调节肠道菌群的结构有关。
Objective
2
To investigate the effect of ginsenoside Rb
1
berberine
and their combination on the intestinal flora in obese mice induced by a high-fat diet.
Methods
2
Forty-two male SPF grade C57BL/6J mice were fed on a high-fat diet for 12 consecutive weeks to establish an obese mice model. The 32 up to the standard obese mice were randomly divided into four groups: the control group
ginsenoside Rb
1
group (20 mg/kg)
berberine group (50 mg/kg)
and ginsenoside Rb
1
+ berberine group (ginsenoside Rb
1
20 mg/kg+ berberine 50 mg/kg)
with eight mice in each group. The mice in each group received the corresponding drugs by gavage for 8 consecutive weeks
and the mice were fed with high-fat diet during the administration period. The body weight of the mice in each group was recorded every week
and the fasting blood glucose of mice in each group was detected every 2 weeks. After the experiment
fecal samples were collected for 16 S rDNA sequencing to observe the changes in the intestinal flora in each group of mice.
Results
2
Compared with the control group
the body weight from 4 to 6 weeks in the ginsenoside Rb
1
group
the berberine group and the ginsenoside Rb
1
+ berberine group were reduced
and the fasting blood glucose at 4
6 and 8 weeks were reduced (
P
<
0.05). Furthermore
the imbalanced intestinal flora induced by the high-fat diet were improved
manifesting as an increased ratio of Bacteroides/Firmicutes
and the relative abundance of harmful bacteria
such as Deferribacteres
Mucispirillum
Helicobacter
Dorea
Ruminococcus
and
Odoribacter
were reduced.
Conclusion
2
Ginsenoside Rb
1
berberine
and their combination could reduce the body weight of mice with diet-induced obesity
and this effect is likely mediated through the modulation of the intestinal flora composition.
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