Document Detail


Dietary anthocyanin-rich bilberry extract ameliorates hyperglycemia and insulin sensitivity via activation of AMP-activated protein kinase in diabetic mice.
MedLine Citation:
PMID:  20089785     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Blueberries or bilberries contain large amounts of anthocyanins, making them one of the richest sources of dietary anthocyanin. These berries are widely consumed as fresh and dried fruits, jams, or juices. Considerable attention has been focused on the health benefits of bilberry fruits beyond their antioxidant content or their ability to improve vision. In this study, we tested the effect of dietary bilberry extract (BBE) on hyperglycemia and insulin sensitivity in type 2 diabetic mice. We found that dietary BBE ameliorates hyperglycemia and insulin sensitivity via activation of AMP-activated protein kinase (AMPK). Dietary BBE significantly reduced the blood glucose concentration and enhanced insulin sensitivity. AMPK was activated in white adipose tissue (WAT), skeletal muscle, and the liver of diabetic mice fed BBE. This activation was accompanied by upregulation of glucose transporter 4 in WAT and skeletal muscle and suppression of glucose production and lipid content in the liver. At the same time, acetyl-CoA carboxylase was inactivated and PPARalpha, acyl-CoA oxidase, and carnitine palmitoyltransferase-1A were upregulated in the liver. These changes resulted in improved hyperglycemia and insulin sensitivity in type 2 diabetes. These findings provide a biochemical basis for the use of bilberry fruits and have important implications for the prevention and treatment of type 2 diabetes via activation of AMPK.
Authors:
Masahito Takikawa; Seiya Inoue; Fumihiko Horio; Takanori Tsuda
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2010-01-20
Journal Detail:
Title:  The Journal of nutrition     Volume:  140     ISSN:  1541-6100     ISO Abbreviation:  J. Nutr.     Publication Date:  2010 Mar 
Date Detail:
Created Date:  2010-02-22     Completed Date:  2010-03-25     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0404243     Medline TA:  J Nutr     Country:  United States    
Other Details:
Languages:  eng     Pagination:  527-33     Citation Subset:  IM    
Affiliation:
College of Bioscience and Biotechnology, Chubu University, Kasugai, Aichi 487-8501, Japan.
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MeSH Terms
Descriptor/Qualifier:
AMP-Activated Protein Kinases / metabolism*
Adiponectin / genetics,  metabolism
Adipose Tissue, White / metabolism
Animals
Anthocyanins / chemistry*,  pharmacology
Blood Glucose
Body Weight
Diabetes Mellitus, Type 2 / drug therapy*
Diet
Eating
Energy Metabolism
Gene Expression Regulation, Enzymologic
Gluconeogenesis
Glucose Transporter Type 4 / genetics,  metabolism
Hyperglycemia / drug therapy*
Insulin Receptor Substrate Proteins / genetics,  metabolism
Insulin Resistance
Liver / metabolism
Male
Mice
Muscle, Skeletal / metabolism
Plant Extracts / chemistry,  pharmacology*
Receptors, Adiponectin / genetics,  metabolism
Retinol-Binding Proteins, Plasma / genetics,  metabolism
Vaccinium myrtillus / chemistry*
Chemical
Reg. No./Substance:
0/Adiponectin; 0/Anthocyanins; 0/Blood Glucose; 0/Glucose Transporter Type 4; 0/Insulin Receptor Substrate Proteins; 0/Irs1 protein, mouse; 0/Plant Extracts; 0/Rbp4 protein, mouse; 0/Receptors, Adiponectin; 0/Retinol-Binding Proteins, Plasma; 0/Slc2a4 protein, mouse; EC 2.7.11.1/AMP-Activated Protein Kinases

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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