Zhang L, Zhang T, Sun J, Huang Y, Liu T, Ye Z, Hu J, Zhang G, Chen H, Ye Z, He Y, Qin J
The Seventh Affiliated Hospital, Sun Yat-Sen University, Shenzhen, 518107, China.
Peking University Shenzhen Hospital, Shenzhen, 518035, China.
J Endocrinol Invest. 2023 Apr;46(4):699-711. doi: 10.1007/s40618-022-01914-3. Epub 2022 Oct 11.
The effects of calorie restriction (CR) on gut microbiota and the mechanism of CR ameliorating hyperglycemia in streptozotocin (STZ)-induced T2DM model rats were explored.
High-fat diet and STZ injection were applied to induce T2DM model rats. Rats were divided into the following three groups: the control-diet ad libitum group, the T2DM model group fed with ad libitum diet, and the T2DM group fed with 30% restriction diet. 16S rRNA sequencing was used to determine the bacterial communities. Lipopolysaccharide (LPS)-binding protein (LBP), interleukin-6 (IL-6), and tumor necrosis factor-α (TNF-α) were measured.
Glucose tolerance and insulin sensitivity were improved by CR, as well as the levels of fasting and random plasma glucose. Besides, CR not only modulated the overall structure of gut microbiota but also had selective enrichment in anti-inflammatory bacteria such as Lachnospiraceae_NK4A136_group, Ruminococcaceae_9, Allobaculum, Alistipes, and Oscillibacter, and decreased pro-inflammatory pathogenic bacteria such as Bacteroides, Lachnoclostridium, and Bifidobacterium. Tax4Fun indicated that CR could regulate related functional pathways such as lipopolysaccharide biosynthesis, and the plasma levels of LBP, IL-6, and TNF-α were markedly reduced by CR, suggesting the mechanism of CR ameliorating hyperglycemia may associate with the modulation of disordered gut microbiota and the reduction of metabolic endotoxemia and inflammation.
CR could ameliorate hyperglycemia, the mechanism of which may associate with the alteration of the overall structure of gut microbiota, restoration of disordered microbiota function, and the downregulation of metabolic endotoxemia and inflammation in diabetic rats.
探讨热量限制(CR)对肠道微生物群的影响以及CR改善链脲佐菌素(STZ)诱导的2型糖尿病(T2DM)模型大鼠高血糖的机制。
采用高脂饮食和注射STZ诱导T2DM模型大鼠。将大鼠分为以下三组:自由摄食对照组、自由摄食的T2DM模型组和30%限制饮食的T2DM组。采用16S rRNA测序确定细菌群落。检测脂多糖(LPS)结合蛋白(LBP)、白细胞介素-6(IL-6)和肿瘤坏死因子-α(TNF-α)。
CR改善了葡萄糖耐量和胰岛素敏感性,以及空腹和随机血糖水平。此外,CR不仅调节了肠道微生物群的整体结构,还选择性富集了抗炎细菌,如毛螺菌科_NK4A136_组、瘤胃球菌科_9、别杆菌属、阿里斯杆菌属和颤杆菌属,并减少了促炎病原菌,如拟杆菌属、毛螺菌属和双歧杆菌属。Tax4Fun表明CR可以调节脂多糖生物合成等相关功能途径,CR显著降低了血浆中LBP、IL-6和TNF-α的水平,提示CR改善高血糖的机制可能与调节紊乱的肠道微生物群、降低代谢性内毒素血症和炎症有关。
CR可以改善高血糖,其机制可能与糖尿病大鼠肠道微生物群整体结构的改变、紊乱的微生物群功能的恢复以及代谢性内毒素血症和炎症的下调有关。