Abstract

There has been a growing interest in hypoglycaemic agents from natural products, especially those derived from plants. In the current survey, hypoglycaemic properties of Persian shallot (Allium hirtifolium Boiss) was evaluated by studying mRNA expression levels of the key enzymes involved in carbohydrate metabolism in liver, Glucokinase (GCK), phosphoenolpyruvate carboxykinase (PEPCK), and glycogen phosphorylase. Thirty two male rats were divided into 4 groups of 8, diabetic groups received 100 and 200 mg/kg Persian shallot extract, diabetic control and normal control received 0.9% saline for 30 days. At the end of the experimental period blood and liver samples were collected. FBS and insulin levels were measured and followed by analysis of the gene expression by Real-Time PCR based methods. Findings indicated that the Persian shallot significantly reduces the FBS level in parallel with slight enhancement of insulin in diabetic rats’ serum. Investigations of gene expression showed that Persian shallot gently increased GCK and glycogen phosphorylase but decreased PEPCK gene activity, in diabetic rats. In conclusion, the data suggest that Persian shallot is an effective hypoglycaemic agent, the observed effect may be via its ability to enhance insulin secretion and GCK gene expression and to decrease hepatic glucose output by reducing PEPCK. Key words: Persian shallot, Glucokinase, glycogen phosphorylase, phosphoenolpyruvate carboxykinase, diabetes.

Highlights

  • Diabetes mellitus is a common metabolic disorder characterized by hyperglycemia due to defects in insulin production and/or function (Abel et al, 2001)

  • Hypoglycaemic properties of Persian shallot (Allium hirtifolium Boiss) was evaluated by studying mRNA expression levels of the key enzymes involved in carbohydrate metabolism in liver, Glucokinase (GCK), phosphoenolpyruvate carboxykinase (PEPCK), and glycogen phosphorylase

  • The data suggest that Persian shallot is an effective hypoglycaemic agent, the observed effect may be via its ability to enhance insulin secretion and GCK gene expression and to decrease hepatic glucose output by reducing PEPCK

Read more

Summary

Introduction

Diabetes mellitus is a common metabolic disorder characterized by hyperglycemia due to defects in insulin production and/or function (Abel et al, 2001). Liver is an insulin-sensitive tissue and plays a major role in maintaining glucose homeostasis via regulating process of the glucose utilization and gluconeogenesis. The liver produces glucose by two pathways, gluconeogenesis (de novo synthesis of glucose) and glycogenolysis (enzymatic break-down of glycogen by glycogen phosphorylase catalytic activity) (Ferre et al, 1996). Insulin suppresses transcription of genes encoding gluconeogenic

Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.