1. Academic Validation
  2. Effect of geniposide, a hypoglycemic glucoside, on hepatic regulating enzymes in diabetic mice induced by a high-fat diet and streptozotocin

Effect of geniposide, a hypoglycemic glucoside, on hepatic regulating enzymes in diabetic mice induced by a high-fat diet and streptozotocin

  • Acta Pharmacol Sin. 2009 Feb;30(2):202-8. doi: 10.1038/aps.2008.17.
Shao-Yu Wu 1 Guang-Fa Wang Zhong-Qiu Liu Jin-Jun Rao Lin Lü Wei Xu Shu-Guang Wu Jia-Jie Zhang
Affiliations

Affiliation

  • 1 School of Pharmaceutical Sciences, Southern Medical University, Guangzhou, China.
Abstract

Aim: Hepatic glycogen phosphorylase (GP) and glucose-6-phosphatase (G6Pase) play an important role in the control of blood glucose homeostasis and are proposed to be potential targets for anti-diabetic drugs. Geniposide is an iridoid glucoside extracted from Gardenia jasminoides Ellis fruits and has been reported to have a hypoglycemic effect. However, little is known about the biochemical mechanisms by which geniposide regulates hepatic glucose-metabolizing Enzymes. The present study investigates whether the hypoglycemic effect of geniposide is mediated by GP or G6Pase.

Methods: Type 2 diabetic mice, induced by a high-fat diet and streptozotocin injection, were treated with or without geniposide for 2 weeks. Blood glucose levels were monitored by a glucometer. Insulin concentrations were analyzed by the ELISA method. Total Cholesterol (TC) and triglyceride (TG) levels were measured using Labassay kits. Activities of hepatic GP and G6Pase were measured by glucose-6-phosphate dehydrogenase-coupled reaction. Real-time RT-PCR and Western blotting were used to determine the mRNA and protein levels of both Enzymes.

Results: Geniposide (200 and 400 mg/kg) significantly decreased the blood glucose, Insulin and TG levels in diabetic mice in a dose-dependent manner. This compound also decreased the expression of GP and G6Pase at mRNA and immunoreactive protein levels, as well as Enzyme activity.

Conclusion: Geniposide is an effective hypoglycemic agent in diabetic mice. The hypoglycemic effect of this compound may be mediated, at least in part, by inhibiting the GP and G6Pase activities.

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