Adlay Bran Oil Suppresses Hepatic Gluconeogenesis and Attenuates Hyperlipidemia in Type 2 Diabetes Rats

J Med Food. 2019 Jan;22(1):22-28. doi: 10.1089/jmf.2018.4237.

Abstract

This study aimed to examine the antidiabetic effects of various concentrations of adlay bran oil (ABO) in high fat diet and streptozotocin-induced diabetic rats. Dietary supplementation with 10% ABO for 4 weeks effectively decreased the blood triacylglycerol, glucose, and total cholesterol levels in diabetic rats, although body weight remained the same. The mRNA and protein expressions of hepatic glucose transporter 2 (GLUT-2) and phosphoenolpyruvate carboxykinase (PEPCK) were increased and that of glucokinase (GCK) were decreased in diabetic rats. However, 10% ABO treatment reduced the mRNA and protein expressions of GLUT-2 and PEPCK and elevated the expression of hepatic GCK in diabetic rats. Thus, ABO enhanced hepatic glucose metabolism to decrease blood glucose in diabetic rats. In addition, 10% ABO supplementation increased the expression of phosphorylated protein kinase B (Akt) relative to the total Akt levels in the muscles of diabetic rats, indicating enhanced insulin sensitivity. The results indicate that ABO displays a potential for improving hyperlipidemia and hyperglycemia in diabetes by enhancing insulin sensitivity and hepatic glucose metabolism.

MeSH terms

  • Animals
  • Blood Glucose / metabolism
  • Coix / chemistry*
  • Diabetes Mellitus, Experimental / complications
  • Diabetes Mellitus, Experimental / drug therapy
  • Diabetes Mellitus, Experimental / metabolism
  • Diabetes Mellitus, Type 2 / complications*
  • Diabetes Mellitus, Type 2 / drug therapy
  • Diabetes Mellitus, Type 2 / metabolism
  • Diet, High-Fat
  • Glucokinase / metabolism
  • Gluconeogenesis / drug effects*
  • Glucose Transporter Type 2 / metabolism
  • Hyperglycemia / blood
  • Hyperglycemia / prevention & control*
  • Hyperlipidemias / blood
  • Hyperlipidemias / prevention & control*
  • Hypoglycemic Agents / pharmacology
  • Hypoglycemic Agents / therapeutic use
  • Hypolipidemic Agents / pharmacology
  • Hypolipidemic Agents / therapeutic use
  • Insulin Resistance
  • Lipids / blood
  • Liver / drug effects*
  • Liver / metabolism
  • Male
  • Muscles / metabolism
  • Phosphoenolpyruvate Carboxykinase (ATP) / metabolism
  • Phytotherapy
  • Plant Oils / pharmacology
  • Plant Oils / therapeutic use*
  • Proto-Oncogene Proteins c-akt / metabolism
  • RNA, Messenger / metabolism
  • Rats, Sprague-Dawley

Substances

  • Blood Glucose
  • Glucose Transporter Type 2
  • Hypoglycemic Agents
  • Hypolipidemic Agents
  • Lipids
  • Plant Oils
  • RNA, Messenger
  • Slc2a2 protein, rat
  • Glucokinase
  • Proto-Oncogene Proteins c-akt
  • Phosphoenolpyruvate Carboxykinase (ATP)