New insights into the biological activities of Chrysanthemum morifolium: Natural flavonoids alleviate diabetes by targeting α-glucosidase and the PTP-1B signaling pathway

Eur J Med Chem. 2019 Sep 15:178:108-115. doi: 10.1016/j.ejmech.2019.05.083. Epub 2019 May 30.

Abstract

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.

Keywords: Chrysanthemum morifolium; Diabetes; Flavonoid; PTP-1B signaling; α-Glucosidase.

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Cholesterol / blood
  • Chrysanthemum / chemistry*
  • Cricetulus
  • Diabetes Mellitus, Experimental / chemically induced
  • Diabetes Mellitus, Experimental / drug therapy*
  • Flavonoids / isolation & purification
  • Flavonoids / therapeutic use*
  • Glucose / metabolism
  • Glycoside Hydrolase Inhibitors / isolation & purification
  • Glycoside Hydrolase Inhibitors / therapeutic use*
  • Hypoglycemic Agents / isolation & purification
  • Hypoglycemic Agents / therapeutic use*
  • Male
  • Mice
  • Protein Tyrosine Phosphatase, Non-Receptor Type 1 / metabolism
  • Rats
  • Signal Transduction / drug effects*
  • Streptozocin
  • Triglycerides / blood

Substances

  • Flavonoids
  • Glycoside Hydrolase Inhibitors
  • Hypoglycemic Agents
  • Triglycerides
  • Streptozocin
  • Cholesterol
  • Protein Tyrosine Phosphatase, Non-Receptor Type 1
  • Glucose