Asiaticoside attenuates memory impairment induced by transient cerebral ischemia-reperfusion in mice through anti-inflammatory mechanism

被引:81
作者
Chen, She [1 ]
Yin, Zhu-Jun [1 ]
Jiang, Chen [2 ]
Ma, Zhan-Qiang [1 ]
Fu, Qiang [1 ]
Qu, Rong [3 ]
Ma, Shi-Ping [1 ]
机构
[1] China Pharmaceut Univ, Dept Pharmacol Chinese Mat Med, Nanjing 210009, Jiangsu, Peoples R China
[2] China Pharmaceut Univ, Dept Clin Pharm, Nanjing 210009, Jiangsu, Peoples R China
[3] Nanjing Univ Chinese Med, Discipline Chinese & Western Integrat Med, Nanjing 210046, Jiangsu, Peoples R China
关键词
Asiaticoside; Cerebral ischemia; Reperfusion; Memory impairment; Inflammation; NITRIC-OXIDE SYNTHASE; OXIDATIVE STRESS; D-GALACTOSE; RAT MODEL; P38; MAPK; BRAIN; ACTIVATION; PATHWAY; INFLAMMATION; INHIBITION;
D O I
10.1016/j.pbb.2014.03.004
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
010107 [宗教学]; 030301 [社会学]; 070906 [古生物学及地层学(含古人类学)];
摘要
Asiaticoside (AS) is isolated from Centella asiatica (L.) which has been using for a long time as a memory enhancing drug in India. This study was to investigate the effects of AS on memory impairment and inflammatory cytokines expression induced by transient cerebral ischemia and reperfusion in mice, as well as the potential signaling pathway. Transient bilateral common carotid artery occlusion (tBCCAO) induced severe memory deficits in mice according to the Morris water maze task and the step-down passive avoidance test. Meanwhile the microglial activation and the gene expression of inflammatory cytokines including interleukin (IL)-1 beta, interleukin (IL)-6 and tumor necrosis factor (TNE)-alpha were increased in the hippocampus of the mice with cerebral ischemia and reperfusion. Oral administration of AS (40 and 60 mg/kg, once per day, started the day after surgery and lasted for 7 days) significantly ameliorated the memory impairment and the inflammation. Moreover, AS (20,40 and 60 mg/kg) markedly reduced the microglial overactivation and the phosphorylation of p38 MAPK in hippocampus compared with the transient cerebral ischemia and reperfusion group. These results suggested that AS showed the neuroprotective effect against transient cerebral ischemia and reperfusion in mice, and this effect might be associated with the anti-inflammation effect of AS via inhibiting overactivation of p38 MAPK pathway. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:7 / 15
页数:9
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