Graduate Diploma and Professional Master in Medical Sciences, Postgraduate Medical Education, School of Medicine, Queen's University, Kingston, ON K7L 3N6, Canada.
Department of Biomedical and Molecular Sciences, Queen's University, Kingston, ON K7L 3N6, Canada.
Nutrients. 2019 Mar 16;11(3):644. doi: 10.3390/nu11030644.
Individuals widely use non-nutritive sweeteners (NNS) in attempts to lower their overall daily caloric intake, lose weight, and sustain a healthy diet. There are insufficient scientific data that support the safety of consuming NNS. However, recent studies have suggested that NNS consumption can induce gut microbiota dysbiosis and promote glucose intolerance in healthy individuals that may result in the development of type 2 diabetes mellitus (T2DM). This sequence of events may result in changes in the gut microbiota composition through microRNA (miRNA)-mediated changes. The mechanism(s) by which miRNAs alter gene expression of different bacterial species provides a link between the consumption of NNS and the development of metabolic changes. Another potential mechanism that connects NNS to metabolic changes is the molecular crosstalk between the insulin receptor (IR) and G protein-coupled receptors (GPCRs). Here, we aim to highlight the role of NNS in obesity and discuss IR-GPCR crosstalk and miRNA-mediated changes, in the manipulation of the gut microbiota composition and T2DM pathogenesis.
人们广泛使用非营养性甜味剂(NNS)来试图降低他们的总日卡路里摄入量、减肥和维持健康饮食。目前还没有足够的科学数据来支持食用 NNS 的安全性。然而,最近的研究表明,NNS 的消耗会导致肠道微生物群落失调,并促进健康个体的葡萄糖不耐受,这可能导致 2 型糖尿病(T2DM)的发生。这一系列事件可能通过 microRNA(miRNA)介导的变化导致肠道微生物群落组成的变化。miRNA 改变不同细菌物种基因表达的机制为 NNS 的消耗与代谢变化的发展之间提供了联系。将 NNS 与代谢变化联系起来的另一个潜在机制是胰岛素受体(IR)和 G 蛋白偶联受体(GPCR)之间的分子串扰。在这里,我们旨在强调 NNS 在肥胖中的作用,并讨论 IR-GPCR 串扰和 miRNA 介导的变化,以操纵肠道微生物群落组成和 T2DM 的发病机制。