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Ingestion of a moderate high‐sucrose diet results in glucose intolerance with reduced liver glucokinase activity and impaired glucagon‐like peptide‐1 secretion
Authors:Eriko Sakamoto  Yusuke Seino  Ayako Fukami  Naohiro Mizutani  Shin Tsunekawa  Kota Ishikawa  Hidetada Ogata  Eita Uenishi  Hideki Kamiya  Yoji Hamada  Hiroyuki Sato  Norio Harada  Yukiyasu Toyoda  Ichitomo Miwa  Jiro Nakamura  Nobuya Inagaki  Yutaka Oiso  Nobuaki Ozaki
Affiliation:1. Department of Endocrinology and Diabetes, Field of Internal Medicine, Nagoya University Graduate School of Medicine;2. Department of Metabolic Medicine, Nagoya University School of Medicine;3. Diabetes Center, Aichi Medical University, Nagakute;4. Department of Pathobiochemistry, Faculty of Pharmacy, Meijo University;5. Department of Diabetes and Clinical Nutrition, Graduate School of Medicine, Kyoto University, Kyoto, Japan;6. Research Center of Health, Physical Fitness and Sports, Nagoya University, Nagoya
Abstract:
Aims/Introduction: Excessive intake of sucrose can cause severe health issues, such as diabetes mellitus. In animal studies, consumption of a high‐sucrose diet (SUC) has been shown to cause obesity, insulin resistance and glucose intolerance. However, several in vivo experiments have been carried out using diets with much higher sucrose contents (50–70% of the total calories) than are typically ingested by humans. In the present study, we examined the effects of a moderate SUC on glucose metabolism and the underlying mechanism. Materials and Methods: C57BL/6J mice received a SUC (38.5% sucrose), a high‐starch diet (ST) or a control diet for 5 weeks. We assessed glucose tolerance, incretin secretion and liver glucose metabolism. Results: An oral glucose tolerance test (OGTT) showed that plasma glucose levels in the early phase were significantly higher in SUC‐fed mice than in ST‐fed or control mice, with no change in plasma insulin levels at any stage. SUC‐fed mice showed a significant improvement in insulin sensitivity. Glucagon‐like peptide‐1 (GLP‐1) secretion 15 min after oral glucose administration was significantly lower in SUC‐fed mice than in ST‐fed or control mice. Hepatic glucokinase (GCK) activity was significantly reduced in SUC‐fed mice. During the OGTT, the accumulation of glycogen in the liver was suppressed in SUC‐fed mice in a time‐dependent manner. Conclusions: These results indicate that mice that consume a moderate SUC show glucose intolerance with a reduction in hepatic GCK activity and impairment in GLP‐1 secretion. (J Diabetes Invest, doi: 10.1111/j.2040‐1124.2012.00208.x , 2012)
Keywords:Glucagon‐like peptide‐1  Glucokinase  High‐sucrose diet
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