Germinated Waxy Black Rice Ameliorates Hyperglycemia and Dyslipidemia in Streptozotocin-Induced Diabetic Rats

被引:14
作者
Kang, Hye Won [1 ]
Kim, Won-Chul [2 ,3 ]
Lee, Jin-Kyu [4 ,7 ]
Ho, Jin-Nyoung [5 ]
Lim, Eun-Jeong [6 ]
Cho, Hong-Yon [4 ]
机构
[1] North Carolina Agr & Tech State Univ, Dept Family & Consumer Sci, Food & Nutr Sci, Greensboro, NC 27411 USA
[2] Dankook Univ, Coll Med, Lab Mol Oncol, Cheil Gen Hosp, Seoul 04619, South Korea
[3] Dankook Univ, Coll Med, Womens Healthcare Ctr, Seoul 04619, South Korea
[4] Korea Univ, Dept Food & Biotechnol, Sejong 30019, South Korea
[5] Seoul Natl Univ, Bundang Hosp, Dept Urol, Seongnam 13620, South Korea
[6] Hanyang Womens Univ, Dept Food & Nutr, Seoul 04763, South Korea
[7] Kolmar BNH, Food Sci R&D Ctr, Sejong 30003, South Korea
基金
新加坡国家研究基金会;
关键词
anti-diabete; germinated waxy black rice; glucose uptake; streptozotocin-induced diabetic rat; GLYCOGEN-SYNTHASE KINASE-3; SATIVA L. INDICA; INSULIN-RESISTANCE; STICKY RICE; EXTRACT; MICE; CELLS; HYPERLIPIDEMIA; SENSITIVITY; SUPPRESSES;
D O I
10.1248/bpb.b17-00239
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This study aimed to examine the anti-diabetic effect of germinated waxy black rice (GWBR) using streptozotocin (STZ)-induced diabetic rats. In the diabetic rats, GWBR supplementation for 8 weeks reduced plasma blood glucose concentrations, improved glucose clearance and prevented diabetes-induced weight loss. Rats with STZ-induced diabetes who received GWBR supplementation exhibited decreased expression of sodium-dependent glucose transporter 1 (SGLT1) and glucose transporter (GLUT) 2 genes and proteins in the small intestine via decreases in hepatocyte nuclear factor (HNF)-1 alpha, HNF-1 beta, and HNF-4 alpha, transcriptional factors that are involved in the regulation of SGLT1 and GLUT2, compared with the rats with STZ-induced diabetes that did not receive GWBR supplements. GWBR supplementation also enhanced the expression of GLUT4 and the genes and proteins involved in GLUT4 translocation, such as insulin receptor (IR) and insulin receptor substrate 1 (IRS1), and increased the phosphorylation of phosphoinositide 3-kinase (PI3K) and protein kinase B (PKB, Akt) proteins in skeletal muscle. GWBR further increased glycogen synthase (GS) 1 by decreasing glycogen synthase kinase (GSK)-3 beta in skeletal muscle. Interestingly, GWBR recovered STZ-impaired pancreatic beta-cells, resulting in increased insulin synthesis and secretion. In addition, GWBR reduced serum triglyceride, total cholesterol, low-density lipoprotein cholesterol, aspartate transferase and alanine transferase concentrations and increased high-density lipoprotein cholesterol concentrations. Taken together, these findings suggest that GWBR could be a candidate for improving the diabetic condition by regulating glucose uptake in the intestine and muscle and regulating the secretion of insulin from the pancreas.
引用
收藏
页码:1846 / 1855
页数:10
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