Therapeutic potential of 20(S)-ginsenoside Rg3 against streptozotocin-induced diabetic renal damage in rats

被引:59
作者
Kang, Ki Sung [1 ]
Yamabe, Noriko [1 ]
Kim, Hyun Young [2 ]
Park, Jeong Hill [2 ]
Yokozawa, Takako [1 ]
机构
[1] Toyama Univ, Inst Nat Med, Toyama 9300194, Japan
[2] Seoul Natl Univ, Coll Pharm, Seoul 151742, South Korea
关键词
advanced glycation endproduct; oxidative stress; N-methyl-D-aspartate receptor; 20(S)-ginsenoside Rg(3); streptozotocin-induced diabetes;
D O I
10.1016/j.ejphar.2008.06.077
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
The inhibitors of advanced glycation endproduct and oxidative stress, as well as N-methyl-D-aspartate (NMDA) receptor antagonists have received considerable interest because of their close association with renoprotective effects. The therapeutic potential of 20(S)-ginsenoside Rg(3) (20(S)-Rg(3)), isolated from Panax ginseng, against streptozotocin-induced diabetic renal damage, was investigated in this study. The diabetic rats received 5, 10, and 20 mg/kg body weight/day of 20(S)-Rg(3) orally via gavage for fifteen consecutive days. The physiological abnormalities such as increases in water intake and urine volume of diabetic rats were significantly decreased by the 20 mg/kg body weight of 20(S)-Rg(3) administration. The elevated serum glucose, glycosylated protein, and thiobarbituric acid-reactive substance levels in diabetic rats were also significantly reduced by the 20(S)-Rg(3) administrations. Moreover, the renal dysfunction of diabetic rats was significantly ameliorated by the 20(S)-Rg(3) administrations in a dose-dependent manner. These beneficial effects on diabetic renal damage were related to the inhibitory effect of 20(S)-Rg(3) against NMDA receptor-mediated nitrosative stress. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:266 / 272
页数:7
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