Water extract of Aralia elata prevents cataractogenesis in vitro and in vivo

被引:50
作者
Chung, YS
Choi, YH
Lee, SJ
Choi, SA
Lee, JH
Kim, H
Hong, EK
机构
[1] Medvill Res Lab, Seoul 110848, South Korea
[2] Seoul Natl Univ, Dept Food & Nutr, Seoul 151742, South Korea
关键词
Aralia elata; anticataract; diabetes; aldose reductase inhibitor; antioxidant; lens culture; diabetic animal;
D O I
10.1016/j.jep.2005.03.020
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The water extract of Aralia elata (Aralia extract) has been used in Korean traditional medicine to treat diabetes mellitus. Here, we investigated the aldose reductase inhibitory activity, antioxidant activity and anticataract capacity of Aralia extract using various experimental systems. To determine its aldose reductase inhibitory activity and its antioxidant effect, we used rat lens homogenates. Rat lens cultures and a rat model were used to observe anticataract activity. The resulting IC50 value of Aralia extract in vitro as an aldose reductase inhibitor was 11.3 mu g/ml and as an antioxidant was 25.1 mu g/ml. Rat lenses in media containing 20 mM xylose developed a distinctly opaque ring in 9 h, and treatment with Aralia extract at a concentration of 1 mg/ml lowered lens opacity by 36.4 and 31.3% after 24 and 48 h, respectively. In vivo experiments were performed with streptozotocin (STZ) induced diabetic rats. The diabetic control animals developed cataracts at 11 weeks after STZ injection, while oral Aralia extract administered at 300 and 600 mg/kg body weight for 11 weeks reduced cataract formation by 15 and 12%, respectively. The present study shows that Aralia extract inhibits aldose reductase and acts in vitro as an antioxidant, and suggests that these activities have a preventive effect on cataractogenesis in xylose containing lens organ cultures and in in vivo in STZ induced diabetic rats. (C) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:49 / 54
页数:6
相关论文
共 33 条
[1]  
*AAALAC, 1996, GUID CAR US LAB AN I
[2]  
AHN DK, 1998, ILLUSTRATED BOOK KOR, P720
[3]   Oxidative protein damage in human diabetic eye: Evidence of a retinal participation [J].
Altomare, E ;
Grattagliano, I ;
Vendemaile, G ;
MicelliFerrari, T ;
Signorile, A ;
Cardia, L .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 1997, 27 (02) :141-147
[4]  
BIRKS JW, 1989, CHROMATOGRAPHY, P10
[5]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[6]   SUGAR CATARACTS INVITRO - IMPLICATIONS OF OXIDATIVE STRESS AND ALDOSE REDUCTASE-I [J].
CHAND, D ;
ELAGUIZY, HK ;
RICHARDS, RD ;
VARMA, SD .
EXPERIMENTAL EYE RESEARCH, 1982, 35 (05) :491-497
[7]   Contribution of polyol pathway to diabetes-induced oxidative stress [J].
Chung, SSM ;
Ho, ECM ;
Lam, KSL ;
Chung, SK .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2003, 14 :S233-S236
[8]  
CHUNG YS, 2002, ENV MUTAGENS CARCINO, V22, P319
[9]  
CHYLACK LT, 1979, OPHTHALMOLOGY, V86, P1579
[10]  
COLLIER A, 1991, BRIT J HOSP MED, V45, P38