Hu Shiwei, Chang Yaoguang, Wang Jingfeng, Xue Changhu, Li Zhaojie, Wang Yuming
College of Food Science and Engineering, Ocean University of China.
Biosci Biotechnol Biochem. 2013;77(11):2263-8. doi: 10.1271/bbb.130529. Epub 2013 Nov 7.
This study investigated the effects of a combination of fucosylated chondroitin sulfate (CHS) and rosiglitazone (RSG) on glucose metabolism in the liver of insulin-resistant C57BL/6J mice fed a high-fat high-sucrose diet for 19 weeks. The results showed that the combination (CHS/RSG) synergistically improved body weight gain, liver weight, fasting blood glucose levels, glucose tolerance on an oral glucose tolerance test, serum insulin levels, homeostasis model assessment indexes, and hepatic glycogen content. In liver tissue, CHS/RSG significantly normalized the activities of hexokinase, pyruvate kinase, and glucose-6-phosphatase. In additionally, it increased the mRNA expression of insulin receptors, insulin receptor substrate 2, phosphatidylinositol 3 kinase (PI3K), protein kinase B (PKB), and glycogen synthase, and inhibited glycogen synthase kinase 3β(GSK-3β) mRNA expression in the liver. This suggests that CHS/RSG treatment improves glucose metabolism by modulating metabolic enzymes and strengthening the PI3K/PKB/GSK-3β signal pathway mediated by insulin at the transcriptional level.
本研究调查了岩藻糖基化硫酸软骨素(CHS)与罗格列酮(RSG)联合使用对喂食高脂高糖饮食19周的胰岛素抵抗C57BL/6J小鼠肝脏葡萄糖代谢的影响。结果表明,联合用药(CHS/RSG)协同改善了体重增加、肝脏重量、空腹血糖水平、口服葡萄糖耐量试验中的葡萄糖耐量、血清胰岛素水平、稳态模型评估指标以及肝糖原含量。在肝脏组织中,CHS/RSG显著使己糖激酶、丙酮酸激酶和葡萄糖-6-磷酸酶的活性恢复正常。此外,它增加了肝脏中胰岛素受体、胰岛素受体底物2、磷脂酰肌醇3激酶(PI3K)、蛋白激酶B(PKB)和糖原合酶的mRNA表达,并抑制了糖原合酶激酶3β(GSK-3β)的mRNA表达。这表明CHS/RSG治疗通过调节代谢酶和在转录水平增强胰岛素介导的PI3K/PKB/GSK-3β信号通路来改善葡萄糖代谢。