Modulatory effect of isopulegol on hepatic key enzymes of glucose metabolism in high-fat diet/streptozotocin-induced diabetic rats

Arch Physiol Biochem. 2021 Aug;127(4):318-326. doi: 10.1080/13813455.2019.1638415. Epub 2019 Jul 10.

Abstract

To investigate the antidiabetic effect of isopulegol in high-fat diet (HFD)/streptozotocin (STZ)-induced diabetic rats. Animals were made diabetic by feeding HFD for 4 weeks followed by single intraperitoneal injection of STZ (35 mg/kg b.w.; 0.1 M citrate buffer; pH 4.0). Plasma insulin, haemoglobin and glycogen content were decreased while increased glucose and glycated haemoglobin were observed in diabetic rats. An increase in glucose-6-phosphatase, fructose-1,6-bisphosphatase, phosphoenol pyruvate carboxykinase with a decrease in hexokinase, glucose-6-phosphate dehydrogenase and glycogen synthase activities was observed in diabetic rats. The expression of cyclic response element binding protein (CREB) was increased in the hepatic tissue of diabetic rats. Isopulegol dose dependently (50, 100 and 200 mg/kg b.w.) improved insulin secretion, glucose tolerance and decreased glucose levels in diabetic-treated rats. At the effective dose of 100 mg/kg b.w., isopulegol restored the activities of metabolic enzymes and down-regulated CREB expression. Thus, isopulegol restored glucose homeostasis through its insulinotrophic property.

Keywords: CREB; Isopulegol; PEPCK; carbohydrate metabolic enzymes; diabetes mellitus.

MeSH terms

  • Animals
  • Antibiotics, Antineoplastic / toxicity
  • Blood Glucose / analysis*
  • Carbohydrate Metabolism / drug effects*
  • Cyclohexane Monoterpenes / pharmacology*
  • Diabetes Mellitus, Experimental / drug therapy*
  • Diabetes Mellitus, Experimental / etiology
  • Diabetes Mellitus, Experimental / pathology
  • Diet, High-Fat / adverse effects*
  • Fructose-Bisphosphatase / metabolism
  • Glucose-6-Phosphatase / metabolism
  • Hexokinase / metabolism
  • Hypoglycemic Agents / pharmacology
  • Insulin / blood
  • Liver / enzymology*
  • Male
  • Rats
  • Rats, Wistar
  • Streptozocin / toxicity*

Substances

  • Antibiotics, Antineoplastic
  • Blood Glucose
  • Cyclohexane Monoterpenes
  • Hypoglycemic Agents
  • Insulin
  • isopulegol
  • Streptozocin
  • Hexokinase
  • Fructose-Bisphosphatase
  • Glucose-6-Phosphatase