Semaglutide alleviates gut microbiota dysbiosis induced by a high-fat diet

阿克曼西亚 赛马鲁肽 失调 肠道菌群 内科学 生物 饮食性肥胖 体重增加 脂肪组织 肥胖 胰岛素抵抗 拟杆菌 免疫学 内分泌学 医学 体重 糖尿病 细菌 2型糖尿病 利拉鲁肽 遗传学
作者
Xinhao Duan,Lei Zhang,Yi Liao,Zijing Lin,Changxin Guo,Sen Luo,Fu Wang,Zhen Zou,Zhijun Zeng,Chengzhi Chen,Jingfu Qiu
出处
期刊:European Journal of Pharmacology [Elsevier BV]
卷期号:969: 176440-176440 被引量:9
标识
DOI:10.1016/j.ejphar.2024.176440
摘要

This study investigated the effects of semaglutide (Sema) on the gut microbiota of obese mice induced with high-fat diet (HFD). Male C57BL/6 J mice aged 6 weeks were enrolled and randomly distributed to four groups, which were provided with a normal control diet (NCD,NCD + Sema) and a 60% proportion of a high-fat diet (HFD,HFD + Sema), respectively. HFD was given for 10 weeks to develop an obesity model and the intervention was lasted for 18 days. The results showed semaglutide significantly reduced body weight gain, areas under the curve (AUC) of glucose tolerance test and insulin resistance test, as well as adipose tissue weight in mice. Semaglutide effectively reduced lipid deposition and lipid droplet formation in the liver of obese mice, and regulated the expression of genes related to abnormal blood glucose regulation. Additionally, semaglutide influenced the composition of gut microbiota, mitigating the microbial dysbiosis induced by a high-fat diet by impacting the diversity of the gut microbiota. After the high-fat diet intervention, certain strains such as Akkermansia, Faecalibaculum, and Allobaculum were significantly decreased, while Lachnospiraceae and Bacteroides were significantly increased. However, the application of semaglutide restored the lost flora and suppressed excessive bacterial abundance. Moreover, semaglutide increased the content of tight junction proteins and repaired the damage to intestinal barrier function caused by the high-fat diet intervention. Furthermore, correlation analysis revealed inverse relationship among Akkermansia levels and weight gain, blood glucose levels, and various obesity indicators. Correlation analysis also showed that Akkermansia level was negatively correlated with weight gain, blood glucose levels and a range of obesity indicators. This phenomenon may explain the anti-obesity effect of semaglutide, which is linked to alterations in gut microbiota, specifically an increase in the abundance of Akkermansia. In summary, our findings indicate that semaglutide has the potential to alleviate gut microbiota dysbiosis, and the gut microbiota may contribute to the obesity-related effects of this drug.
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