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High Fat Diet and High Sucrose Intake Divergently Induce Dysregulation of Glucose Homeostasis through Distinct Gut Microbiota-Derived Bile Acid Metabolism in Mice

肠道菌群 葡萄糖稳态 生物 胆汁酸 碳水化合物代谢 新陈代谢 内分泌学 内科学 双歧杆菌 平衡 乳酸菌 生物化学 细菌 糖尿病 胰岛素抵抗 医学 遗传学
作者
Xiaofang He,Xinxin Gao,Ying Hong,Jing Zhong,Yue Li,Weize Zhu,Junli Ma,Weidong Huang,Yifan Li,Yan Li,Hao Wang,Zexian Liu,Yiyang Bao,Li Wang,Ningning Zheng,Lili Sheng,Houkai Li
出处
期刊:Journal of Agricultural and Food Chemistry [American Chemical Society]
卷期号:72 (1): 230-244 被引量:2
标识
DOI:10.1021/acs.jafc.3c02909
摘要

A high calorie diet such as excessive fat and sucrose intake is always accompanied by impaired glucose homeostasis such as T2DM (type 2 diabetes mellitus). However, it remains unclear how fat and sucrose individually affect host glucose metabolism. In this study, mice were fed with high fat diet (HFD) or 30% sucrose in drinking water (HSD) for 24 weeks, and glucose metabolism, gut microbiota composition, as well as bile acid (BA) profile were investigated. In addition, the functional changes of HFD or HSD-induced gut microbiota were further verified by fecal microbiota transplantation (FMT) and ex vivo culture of gut bacteria with BAs. Our results showed that both HFD and HSD caused dysregulated lipid metabolism, while HFD feeding had a more severe effect on impaired glucose homeostasis, accompanied by reduced hyocholic acid (HCA) levels in all studied tissues. Meanwhile, HFD had a more dramatic influence on composition and function of gut microbiota based on α diversity indices, β diversity analysis, as well as the abundance of secondary BA producers than HSD. In addition, the phenotypes of impaired glucose homeostasis and less formation of HCA caused by HFD can be transferred to recipient mice by FMT. Ex vivo culture with gut bacteria and BAs revealed HFD-altered gut bacteria produced less HCA than HSD, which might closely associate with reduced relative abundance of C7 epimerase-coding bacteria g_norank/unclassified_f_Eggerthellaceae and bile salt hydrolase-producing bacteria Lactobacillus and Bifidobacterium in HFD group. Our findings revealed that the divergent effects of different high-calorie diets on glucose metabolism may be due to the gut microbiota-mediated generation and metabolism of BAs, highlighting the importance of dietary management in T2DM.
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