Hepato-/reno-protective activity of Chinese prescription Kangen-karyu through inhibition of AGE formation and fibrosis-related protein expression in type 2 diabetes

Author:

Okamoto Takuya123,Park Chan Hum1,Noh Jeong Sook1,Toriizuka Kazuo3,Sei Yasuo2,Park Jong Cheol4,Yokozawa Takako1

Affiliation:

1. Institute of Natural Medicine, University of Toyama, Sugitani, Toyama, Japan

2. Iskra Industry Co., Ltd, Nihonbashi, Chuo-ku, Tokyo, Japan

3. School of Pharmaceutical Sciences, Showa University, Hatanodai, Shinagawa-ku, Tokyo, Japan

4. Department of Oriental Medicine Resources and Research Institute of Korean Oriental Medicines, Sunchon National University, Suncheon, Jeonnam, Korea

Abstract

Abstract Objectives This study was conducted to examine whether Kangen-karyu, a Chinese prescription, has an ameliorative effect on diabetes-induced alterations such as advanced glycation endproduct (AGE) formation or the fibrotic response in liver and kidney of type 2 diabetic db/db mice. Methods Kangen-karyu (100 or 200 mg/kg body weight/day, p.o.) was administered every day for 18 weeks to db/db mice, and its effect was compared with vehicle-treated db/db and m/m mice. Key findings The administration of Kangen-karyu decreased the elevated serum glucose concentration in db/db mice. The increased serum creatinine and urea nitrogen levels, which reflect renal dysfunction in db/db mice, were significantly lowered by Kangen-karyu administration. The db/db mice exhibited the up-regulation of AGEs and its receptor expression in liver and kidney; however, Kangen-karyu treatment significantly reduced expression except for the receptor. Moreover, the augmented expressions of fibrosis-related proteins, transforming growth factor (TGF)-β1, fibronectin and collagen IV were down-regulated by Kangen-karyu administration. Conclusions These results provide important evidence that Kangen-karyu exhibits a pleiotropic effect on AGE formation and fibrosis-related parameters, representing hepatoprotective and renoprotective effects against the development of diabetic complications in type 2 diabetic db/db mice.

Publisher

Oxford University Press (OUP)

Subject

Pharmaceutical Science,Pharmacology

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