Key Laboratory of Industrial Fermentation Microbiology of Ministry of Education, China International Science and Technology Cooperation Base of Food Nutrition/Safety and Medicinal Chemistry, Tianjin University of Science and Technology, Tianjin, 300457, China.
Key Laboratory of Industrial Fermentation Microbiology of Ministry of Education, China International Science and Technology Cooperation Base of Food Nutrition/Safety and Medicinal Chemistry, Tianjin University of Science and Technology, Tianjin, 300457, China; Sorbonne Université, Institut Parisien de Chimie Moléculaire, UMR CNRS 8232, 4 place Jussieu, 75005, Paris, France.
Eur J Med Chem. 2019 Sep 15;178:108-115. doi: 10.1016/j.ejmech.2019.05.083. Epub 2019 May 30.
As dual regulators, the PTP-1B signaling pathway and α-glucosidase slow glucose release and increase the degree of insulin sensitivity, representing a promising therapeutic target for type 2 diabetes. In this study, we systematically examined the in vivo and in vitro anti-diabetic activities of natural flavonoids 1-6 from Chrysanthemum morifolium. Flavonoids 1-6 increased glucose consumption-promoting activity and the phosphorylation of GSK-3β and Akt, and decreased PTP-1B protein level along with slightly inhibitory activity of the PTP-1B enzyme. Moreover, flavonoids 1-2 treatment induced insulin secretion in INS-1 cells. Besides, in vivo study revealed that flavonoids 2 and 5 demonstrated potent anti-hyperglycemic and anti-hyperlipidemic activity, and improved maltose and glucose tolerance. Although flavonoid 2 exhibited lower inhibitory activity against α-glucosidase in vitro, it could deglycosylated in vivo to diosmetin to function as an α-glucosidase inhibitor. Taken together, these results led to the identification of the natural flavonoids 1-6 from C. morifolium as dual regulators of α-glucosidase and the PTP-1B signaling pathway, suggesting their potential application as new oral anti-diabetic drugs or functional food ingredients.
作为双重调节剂,PTP-1B 信号通路和 α-葡萄糖苷酶可减缓葡萄糖释放并提高胰岛素敏感性的程度,是治疗 2 型糖尿病的有希望的治疗靶点。在这项研究中,我们系统地研究了来自菊花的天然黄酮类化合物 1-6 的体内和体外抗糖尿病活性。黄酮类化合物 1-6 增加了葡萄糖消耗促进活性和 GSK-3β和 Akt 的磷酸化,并降低了 PTP-1B 蛋白水平,同时对 PTP-1B 酶具有轻微的抑制作用。此外,黄酮类化合物 1-2 处理可诱导 INS-1 细胞胰岛素分泌。此外,体内研究表明,黄酮类化合物 2 和 5 具有很强的降血糖和降血脂活性,并改善了麦芽糖和葡萄糖耐量。尽管黄酮类化合物 2 在体外对 α-葡萄糖苷酶的抑制活性较低,但它可以在体内糖基化生成地奥司明,从而发挥 α-葡萄糖苷酶抑制剂的作用。总之,这些结果表明,菊花中的天然黄酮类化合物 1-6 是 α-葡萄糖苷酶和 PTP-1B 信号通路的双重调节剂,提示它们可能作为新型口服抗糖尿病药物或功能性食品成分得到应用。