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魔芋低聚糖通过改善胰岛素和瘦素抵抗在体外和体内对葡萄糖稳态的影响。

Effect of Konjac Mannan Oligosaccharides on Glucose Homeostasis via the Improvement of Insulin and Leptin Resistance In Vitro and In Vivo.

机构信息

Beijing Advanced Innovation Center for Food Nutrition and Human Health, China Agricultural University, Beijing 100083, China.

Bioresource Utilization Laboratory, College of Engineering, China Agricultural University, Beijing 100083, China.

出版信息

Nutrients. 2019 Jul 24;11(8):1705. doi: 10.3390/nu11081705.

Abstract

Functional oligosaccharides, particularly konjac mannan oligosaccharides (KMOS), can regulate glucose metabolism. However, the molecular mechanisms involved in the hypoglycemic effect of KMOS remain largely unknown. Here, the effect of KMOS supplementation on glucose homeostasis was evaluated in both high-fat diet (HFD)-fed C57BL/6J mice and high-glucosamine-induced HepG2 cells. KMOS supplementation remarkably ameliorated the fasting blood glucose, glucose tolerance, and insulin tolerance of HFD-fed mice. Abnormalities of triglyceride and glycogen metabolism in the liver induced by the HFD were reversed by KMOS supplementation. The insulin signaling pathway was activated by KMOS, with stimulation of GLUT2 membrane translocation and glucose uptake in HepG2 cells via the AMPK pathway. Moreover, KMOS suppressed p-mTOR expression and stimulated the GSK-3β/CREB pathway via the AMPK pathway. KMOS significantly upregulated leptin receptor expression and downregulated PTP1B and SOCS3 levels in the liver and brain, with a decreased serum leptin concentration. Phosphorylation of JAK2 and STAT3 in the liver was activated by KMOS supplementation, while the expressions of Sirt1, Tfam, and Pgc1-α in the brain were elevated. Conclusively, KMOS attenuated HFD-induced glucose metabolism dysfunction through the regulation of insulin resistance and leptin resistance. This finding indicates that KMOS have potential value as an anti-hyperglycemic dietary supplement.

摘要

功能性寡糖,特别是魔芋甘露寡糖(KMOS),可以调节葡萄糖代谢。然而,KMOS 降血糖作用的分子机制在很大程度上尚不清楚。在这里,我们评估了 KMOS 补充对高脂饮食(HFD)喂养的 C57BL/6J 小鼠和高葡萄糖胺诱导的 HepG2 细胞葡萄糖稳态的影响。KMOS 补充显著改善了 HFD 喂养小鼠的空腹血糖、葡萄糖耐量和胰岛素耐量。KMOS 补充逆转了 HFD 引起的肝脏甘油三酯和糖原代谢异常。KMOS 通过 AMPK 通路激活胰岛素信号通路,刺激 HepG2 细胞中 GLUT2 的膜转位和葡萄糖摄取。此外,KMOS 通过 AMPK 通路抑制 p-mTOR 表达并刺激 GSK-3β/CREB 通路。KMOS 显著上调肝脏和脑中瘦素受体的表达,降低血清瘦素浓度,并下调 PTP1B 和 SOCS3 水平。KMOS 补充激活了肝脏中 JAK2 和 STAT3 的磷酸化,同时大脑中 Sirt1、Tfam 和 Pgc1-α 的表达升高。总之,KMOS 通过调节胰岛素抵抗和瘦素抵抗来减轻 HFD 诱导的葡萄糖代谢功能障碍。这一发现表明,KMOS 作为一种抗高血糖膳食补充剂具有潜在的价值。

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