Ginseng Extract Modified by Pectin Lyase Inhibits Retinal Vascular Injury and Blood-Retinal Barrier Breakage in a Rat Model of Diabetes

被引:8
|
作者
Jung, Eunsoo [1 ]
Kim, Chan-Sik [2 ]
Jung, Wookwon [3 ]
Park, Su-Bin [3 ]
Pyo, Mi-Kyung [4 ]
Kim, Junghyun [2 ,3 ]
机构
[1] Seoul Natl Univ, Coll Vet Med, Lab Toxicol, Seoul, South Korea
[2] Korea Inst Oriental Med, Clin Res Div, Daejeon, South Korea
[3] Chonbuk Natl Univ, Sch Dent, Dept Oral Pathol, 567 Baekje Daero, Jeonju 54896, South Korea
[4] Int Ginseng & Herb Res Inst, Geumsan, South Korea
关键词
blood-retinal barrier; diabetic retinopathy; GS-E3D; kwon; GLYCATION END-PRODUCTS; KOREAN RED GINSENG; ENDOTHELIAL GROWTH-FACTOR; PANAX-GINSENG; OXIDATIVE STRESS; SERUM-LEVELS; APOPTOSIS; RETINOPATHY; AMINOGUANIDINE; PROTECTS;
D O I
10.1089/jmf.2018.4256
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
GS-E3D is an enzymatically modified ginseng extract by pectin lyase. In this study, we evaluated the preventive effects of GS-E3D on blood-retinal barrier (BRB) leakage in a rat model of diabetes. To produce diabetes, rats were injected with streptozotocin. GS-E3D was orally gavaged at 25, 50, and 100 mg/kg body weight for 6 weeks. We then compared the effect of GS-E3D with that of an unmodified ginseng extract (UGE) on retinal vascular leakage. The administration of GS-E3D significantly blocked diabetes-induced BRB breakdown. Immunofluorescence staining showed that GS-E3D reduced the loss of occludin in diabetic rats. In TUNEL staining, the number of apoptotic retinal microvascular cells was dose dependently decreased by GS-E3D treatment. GS-E3D decreased the accumulations of advanced glycation end products in the retinal vessels. In addition, the inhibition potential of GS-E3D on BRB breakage was stronger compared with UGE. These results indicate that GS-E3D could be a beneficial treatment option for preventing diabetes-induced retinal vascular injury.
引用
收藏
页码:337 / 343
页数:7
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