Volume 63, Issue 10 pp. 1301-1308
Research Paper

KIOM-79 inhibits aldose reductase activity and cataractogenesis in Zucker diabetic fatty rats

Junghyun Kim

Corresponding Author

Junghyun Kim

Jin Sook Kim, Diabetic Complications Research Center, Division of Traditional Korean Medicine (TKM) Integrated Research, Korea Institute of Oriental Medicine (KIOM), 483 Exporo, Yuseong-gu, Daejeon 305-811, South Korea.E-mail: [email protected]Search for more papers by this author
Chan-Sik Kim

Chan-Sik Kim

Diabetic Complications Research Center, Division of Traditional Korean Medicine Integrated Research, Korea Institute of Oriental Medicine, Daejeon, South Korea

Search for more papers by this author
Eunjin Sohn

Eunjin Sohn

Diabetic Complications Research Center, Division of Traditional Korean Medicine Integrated Research, Korea Institute of Oriental Medicine, Daejeon, South Korea

Search for more papers by this author
Yun Mi Lee

Yun Mi Lee

Diabetic Complications Research Center, Division of Traditional Korean Medicine Integrated Research, Korea Institute of Oriental Medicine, Daejeon, South Korea

Search for more papers by this author
Jin Sook Kim

Jin Sook Kim

Diabetic Complications Research Center, Division of Traditional Korean Medicine Integrated Research, Korea Institute of Oriental Medicine, Daejeon, South Korea

Search for more papers by this author
First published: 16 August 2011
Citations: 10

Abstract

Objectives KIOM-79, a combination of four plant extracts, has a preventive effect on diabetic nephropathy and retinopathy in diabetic animal models. In this study, we have investigated the inhibitory effects of KIOM-79 on diabetic cataractogenesis.

Methods We evaluated aldose reductase activity during cataractogenesis using Zucker diabetic fatty (ZDF) rat, an animal model of type 2 diabetes. ZDF rats were treated orally with KIOM-79 (50 mg/kg body weight) once a day for 13 weeks.

Key findings In vehicle-treated ZDF rats, lens opacity was increased, and lens fibre swelling and membrane rupture were observed. In addition, aldose reductase activity and aldose reductase protein expression in diabetic lens were markedly enhanced. However, the administration of KIOM-79 inhibited the development of diabetic cataract through the inhibition of aldose reductase activity and protein expression in diabetic lenses.

Conclusions These observations suggested that KIOM-79 was useful against the treatment of diabetic cataractogenesis.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.