Ginseng Extracts, GS-KG9 and GS-E3D, Prevent Blood-Brain Barrier Disruption and Thereby Inhibit Apoptotic Cell Death of Hippocampal Neurons in Streptozotocin-Induced Diabetic Rats

被引:14
作者
Lee, Jee Youn [1 ]
Park, Chan Sol [1 ,2 ]
Choi, Hae Young [1 ]
Yune, Tae Young [1 ,2 ,3 ,4 ]
机构
[1] Kyung Hee Univ, Age Related & Brain Dis Res Ctr, Seoul 02447, South Korea
[2] Kyung Hee Univ, Dept Biomed Sci, Seoul 02447, South Korea
[3] Kyung Hee Univ, Sch Med, Dept Biochem & Mol Biol, Seoul 02447, South Korea
[4] Kyung Hee Univ, KHU KIST Dept Converging Sci & Technol, Seoul 02447, South Korea
基金
新加坡国家研究基金会;
关键词
blood-brain barrier; apoptosis; hippocampus; microglia; astrocyte; streptozotocin; FERMENTED RED GINSENG; COGNITIVE IMPAIRMENT; IN-VITRO; PERMEABILITY; DAMAGE; EXPRESSION; INSULIN; INJURY; INFLAMMATION; DYSFUNCTION;
D O I
10.3390/nu12082383
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 [营养与食品卫生学];
摘要
Type 1 diabetes mellitus is known to be linked to the impairment of blood-brain barrier (BBB) integrity following neuronal cell death. Here, we investigated whether GS-KG9 and GS-E3D, bioactive ginseng extracts from Korean ginseng (Panax ginsengMeyer), inhibit BBB disruption following neuronal death in the hippocampus in streptozotocin-induced diabetic rats showing type 1-like diabetes mellitus. GS-KG9 and GS-E3D (50, 150, or 300 mg/kg, twice a day for 4 weeks) administered orally showed antihyperglycemic activity in a dose-dependent manner and significantly attenuated the increase in BBB permeability and loss of tight junction proteins. GS-KG9 and GS-E3D also inhibited the expression and activation of matrix metalloproteinase-9 and the infiltration of macrophages into the brain parenchyma, especially into the hippocampal region. In addition, microglia and astrocyte activation in the hippocampus and the expression of proinflammatory mediators such astnf-alpha,Il-1 beta,IL-6,cox-2, andinoswere markedly alleviated in GS-KG9 and GS-E3D-treated group. Furthermore, apoptotic cell death of hippocampal neurons, especially in CA1 region, was significantly reduced in GS-KG9 and GS-E3D-treated groups as compared to vehicle control. These results suggest that GS-KG9 and GS-E3D effectively prevent apoptotic cell death of hippocampal neurons by inhibiting BBB disruption and may be a potential therapy for the treatment of diabetic patients.
引用
收藏
页码:1 / 18
页数:18
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