Long-Term Consumption of Sucralose Induces Hepatic Insulin Resistance through an Extracellular Signal-Regulated Kinase 1/2-Dependent Pathway

• Published in: Nutrients Vol. 15; no. 12; p. 2814
• Main Authors: Tsai, Meng-Jie, Li, Chung-Hao, Wu, Hung-Tsung, Kuo, Hsin-Yu, Wang, Chung-Teng, Pai, Hsiu-Ling, Chang, Chih-Jen, Ou, Horng-Yih
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 20.06.2023; MDPI
• Subjects: Animals; Artificial sweeteners; blood glucose; Cardiovascular disease; Cell culture; Cell cycle; Cell growth; Dextrose; Diabetes; Diabetes therapy; Diet; Diet, High-Fat - adverse effects; endoplasmic reticulum stress; Enzymes; Glucose; Glucose Intolerance - etiology; glycemic control; high fat diet; Homeostasis; Insulin; Insulin Resistance; insulin secretion; Kinases; Laboratory animals; liver; Liver - metabolism; Lymphocytes; Metabolism; Mice; mitogen-activated protein kinase; Mitogen-Activated Protein Kinase 3; Obesity; Oxidative stress; Proteins; R&D; Research & development; Sucralose; Sweetening Agents - pharmacology; taste receptors; Taiwan; St Louis Missouri; United States > US; Taste 1 receptor member 3; artificial sweetener; insulin resistance; high-fat diet; sucralose
• ISSN: 2072-6643; 2072-6643
• DOI: 10.3390/nu15122814

Sugar substitutes have been recommended to be used for weight and glycemic control. However, numerous studies indicate that consumption of artificial sweeteners exerts adverse effects on glycemic homeostasis. Although sucralose is among the most extensively utilized sweeteners in food products, the effects and detailed mechanisms of sucralose on insulin sensitivity remain ambiguous. In this study, we found that bolus administration of sucralose by oral gavage enhanced insulin secretion to decrease plasma glucose levels in mice. In addition, mice were randomly allocated into three groups, chow diet, high-fat diet (HFD), and HFD supplemented with sucralose (HFSUC), to investigate the effects of long-term consumption of sucralose on glucose homeostasis. In contrast to the effects of sucralose with bolus administration, the supplement of sucralose augmented HFD-induced insulin resistance and glucose intolerance, determined by glucose and insulin tolerance tests. In addition, we found that administration of extracellular signal-regulated kinase (ERK)-1/2 inhibitor reversed the effects of sucralose on glucose intolerance and insulin resistance in mice. Moreover, blockade of taste receptor type 1 member 3 (T1R3) by lactisole or pretreatment of endoplasmic reticulum stress inhibitors diminished sucralose-induced insulin resistance in HepG2 cells. Taken together, sucralose augmented HFD-induced insulin resistance in mice, and interrupted insulin signals through a T1R3-ERK1/2-dependent pathway in the liver.