Neuroprotective effects of a traditional herbal prescription on transient cerebral global ischemia in gerbils

被引:38
|
作者
Cai, Mudan [2 ]
Shin, Bum Young [1 ]
Kim, Dong Hyun [2 ]
Kim, Jong Min [2 ]
Park, Se Jin [2 ]
Park, Chan Sung [3 ]
Won, Do Hee [3 ]
Hong, Nam Doo [3 ]
Kang, Dong Hyo [4 ]
Yutaka, Yamamoto [4 ]
Ryu, Jong Hoon [1 ,2 ]
机构
[1] Kyung Hee Univ, Dept Oriental Pharmaceut Sci, Coll Pharm, Seoul 130701, South Korea
[2] Kyung Hee Univ, Dept Life & Nanopharmaceut Sci, Seoul 130701, South Korea
[3] Kwang Dong Pharmaceut Co Ltd, R&D Ctr, Pyongtaek Si 459020, Kyonggi Do, South Korea
[4] Tochimoto Tenkaido Co Ltd, Kita Ku, Osaka 5300053, Japan
关键词
Kyung-Ok-Ko; Global ischemia; Hippocampal cell death; Inflammation; OXIDATIVE STRESS; BRAIN-INJURY; NEURONAL DEGENERATION; FOREBRAIN ISCHEMIA; FLUORO-JADE; STROKE; DAMAGE; MICE; INFLAMMATION; MECHANISMS;
D O I
10.1016/j.jep.2011.10.016
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Aim of the study: Kyung-Ok-Ko (KOK), a traditional herbal prescription composed of Rehmannia glutinosa var. purpurae, Panax ginseng, Poria cocos, Lycium chinense, Aquillaria agallocha and honey, has been used to treat age-related symptoms, such as amnesia or dementia, and has been shown to ameliorate scopolamine-induced memory impairment in mice. However, the effects of KOK on transient cerebral global ischemia-induced brain damage are unclear. Materials and methods: Transient cerebral global ischemia was induced by occluding the bilateral common carotid artery for 5 min followed by reperfusion for 7 days. KOK (0.25, 0.5, 1, or 2 g/kg) was administered orally immediately after reperfusion and once a day over the next 7 days. Y-maze or novel object recognition tasks were to analyze learning and memory capabilities at 4 or 5 days after reperfusion, respectively. Histochemistry and immunohistochemistry were used for evaluation of the effect of KOK on neuronal degeneration. Results: Histochemical studies showed that KOK increased the number of viable cells detected by Nissl staining and decreased the number of degenerated neuronal cells detected by Fluoro-Jade B staining in the hippocampal CA1 region. In the immunohistochemical study, the sub-chronic KOK administration attenuated the ischemia-induced activation of microglia and astrocytes and the increase of cytokine IL-1 beta (P<0.05). In addition, KOK administration significantly attenuated the ischemia-induced cognitive impairments observed in the Y-maze and novel object recognition tasks (P<0.05). Conclusion: These findings suggest that the neuroprotective effects of KOK may be mediated by its anti-inflammatory activities, resulting in the attenuation of memory impairment. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:723 / 730
页数:8
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