Korean red ginseng (Panax ginseng) improves insulin sensitivity and attenuates the development of diabetes in Otsuka Long-Evans Tokushima fatty rats

被引:85
作者
Lee, Hyun Joo
Lee, Yong-ho [2 ]
Park, Sang Kyu [3 ]
Kang, Eun Seok [4 ]
Kim, Hyo-Jeong [5 ]
Lee, Young Chul [6 ]
Choi, Cheol Soo [7 ]
Park, Se Eun
Ahn, Chul Woo [4 ]
Cha, Bong Soo [4 ]
Lee, Kwan Woo [8 ]
Kim, Kyung-Sup [3 ]
Lim, Sung Kil [2 ,4 ]
Lee, Hyun Chul [1 ,2 ,4 ]
机构
[1] Yonsei Univ, Dept Internal Med, Div Endocrinol & Metab, Coll Med, Seoul 120752, South Korea
[2] Yonsei Univ, Dept Med, Grad Sch, Coll Med, Seoul 120752, South Korea
[3] Yonsei Univ, Dept Biochem & Mol Biol, Coll Med, Seoul 120752, South Korea
[4] Yonsei Univ, Brain Korea Project Med Sci 21, Coll Med, Seoul 120752, South Korea
[5] Eulgi Univ, Coll Med, Dept Internal Med, Taejon 301110, South Korea
[6] Korea Food Res Inst, Songnam 463746, South Korea
[7] Gachon Univ Med & Sci, Korean Mouse Metab Phenotyping Ctr, Inchon 406799, South Korea
[8] Ajou Univ, Sch Med, Dept Endocrinol, Suwon 443380, South Korea
来源
METABOLISM-CLINICAL AND EXPERIMENTAL | 2009年 / 58卷 / 08期
关键词
ACTIVATED PROTEIN-KINASE; SKELETAL-MUSCLE; MITOCHONDRIAL DYSFUNCTION; POSTPRANDIAL GLYCEMIA; AMERICAN GINSENG; OBESITY; RESISTANCE; GLUCOSE; METABOLISM; OXIDATION;
D O I
10.1016/j.metabol.2009.03.015
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Ginseng has been reported to ameliorate hyperglycemia in experimental and clinical studies;, however, its mechanism of action remains unclear. In this study, we investigated the metabolic effects and Putative molecular mechanisms of Korean red ginseng (KRG, Panax ginseng) in animal models for type 2 diabetes mellitus (T2DM) and peripheral insulin-responsive cell lines. Korean red ginseng was administered orally Lit a dose of 200 mg/(kg d) to Otsuka Long-Evans Tokushima fatly rats for 40 weeks. Initially, chronic administration of KRG reduced weight gain and visceral far mass in the early period Without altering food intake. The KRG-treated Otsuka Long-Evans Tokushima fatty rats showed improved insulin sensitivity and significantly preserved glucose tolerance compared with untreated control animals LIP to 50 weeks of age, implying that KRG attenuated the development of overt diabetes. KRG promoted fatty acid oxidation by the activation of adenosine monophosphate-activated protein kinase (AMPK) and phosphorylation of acetyl-coenzyme A carboxylase in skeletal Muscle and Cultured C2C12 muscle cells. Increased expression of peroxisome proliferator-activated receptor-gamma coactivator-la, nuclear respiratory factor-1, cytochrome c, cytochrorne c oxidase-4, and glucose transporter 4 by KRG treatment indicates that activated AMPK also enhanced mitochondrial biogenesis and glucose utilization in skeletal muscle. Although these findings suggest that KRG is likely to have beneficial effects on the amelioration of insulin resistance and the prevention of T2DM through the activation of AMPK, further clinical studies are required to evaluate the use of KRG as a supplementary agent for T2DM. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:1170 / 1177
页数:8
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