A comparative study of the antidiabetic effects exerted by live and dead multi-strain probiotics in the type 2 diabetes model of mice

被引:57
|
作者
Li, Xiangfei [1 ,2 ]
Xu, Qi [1 ,2 ]
Jiang, Tian [3 ]
Fang, Shuguang [3 ]
Wang, Gang [1 ,2 ]
Zhao, Jianxin [1 ,2 ]
Zhang, Hao [1 ,2 ]
Chen, Wei [1 ,2 ,4 ]
机构
[1] Jiangnan Univ, State Key Lab Food Sci & Technol, Sch Food Sci Technol, Wuxi 214122, Peoples R China
[2] Jiangnan Univ, Int Joint Res Lab Probiot, Wuxi 214122, Peoples R China
[3] Jiangsu Wecare Biotechnol Co Ltd, Wujiang 215200, Peoples R China
[4] Beijing Technol & Business Univ, Beijing Innovat Ctr Food Nutr & Human Hlth, Beijing 100048, Peoples R China
基金
中国国家自然科学基金;
关键词
HIGH-FAT DIET; LACTOBACILLUS-PLANTARUM NCU116; GUT MICROBIOTA; METABOLIC SYNDROME; GLUCOSE-TOLERANCE; CASEI; MODULATION; SECRETION; FERMENTUM; REUTERI;
D O I
10.1039/c6fo01147k
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Type 2 diabetes is a metabolic syndrome characterized by insulin resistance and relative insulin deficiency. In this study, the anti-diabetic effects of live and dead multi-strain probiotics were explored and compared in a high-fat and streptozotocin-induced model of type 2 diabetes in mice. Either live or dead probiotics were daily administered orally to the mice over 10 weeks. Both live and dead multi-strain probiotics reduced HbA1C and leptin levels, improved glucose tolerance, and protected against the impairment of the pancreas, while the live probiotic showed a greater ability to reduce fasting and postprandial blood glucose levels. In addition, the live multi-strain probiotic exerted the beneficial effect of ameliorating insulin resistance. This effect was associated with the gut microbiota, butyrate production, and the inflammatory response, and was more effective for the live probiotic than the dead probiotic. These findings showed that the viable probiotic more effectively relieved hypoglycemic symptoms in the host by ameliorating insulin resistance. Furthermore, a pathway related to insulin resistance, i. e., the gut microbiotabutyrate- inflammatory axis, provided a promising rationale for further research into preventing or treating type 2 diabetes.
引用
收藏
页码:4851 / 4860
页数:10
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