Neuroprotective effects of a standardized extract of Diospyros kaki leaves on MCAO transient focal cerebral ischemic rats and cultured neurons injured by glutamate or hypoxia

被引:40
作者
Bei, Weijian
Peng, Wenlie
Zang, Linquan
Xie, Zhiyong
Hu, Dehui
Xu, Anlong
机构
[1] Sun Yat Sen Univ, Sch Life Sci, Dept Biochem, Key Lab Genet Engn MOE, Guangzhou 510275, Guangdong, Peoples R China
[2] Guangzhou Pharmaceut Univ, Inst Tradit Chinese Med, Guangzhou Higher Educ Mega Ctr, Guangzhou, Peoples R China
[3] Hutchison Whampoa Guangzhou Baiyunshan Chinese Me, Inst Modern TCM, Guangzhou, Peoples R China
[4] Sun Yat Sen Univ, Sch Med, Dept Pharmacol, Guangzhou, Peoples R China
[5] Sun Yat Sen Univ, Sch Pharmaceut Sci, Guangzhou, Peoples R China
[6] Nanfang Med Univ, Sch Med, Dept Physiol, Guangzhou, Peoples R China
关键词
Naoxinqing; Diospyros kaki L; CNS pharmacology; neuroprotection; middle cerebral artery occlusion; ischemia and reperfusion; glutamate; hypoxia;
D O I
10.1055/s-2007-981532
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Naoxinqing (NXQ, a standardized extract of Diospyros kaki leaves) is a patented and approved drug of Traditional Chinese Medicine (TCM) used for the treatment of apoplexy syndrome for years in China, but its underlying mechanism remains to be further elucidated. The present study investigates the effects of NXQ against focal ischemia/reperfusion injury induced by middle cerebral artery occlusion (MCAO) in rats and against glutamate-induced cell injury of hippocampal neurons as well as against hypoxia injury of cortical neurons. Oral administrations of NXQ at 20, 40, 80 mg/kg/day for 7 days (3 days before MCAO and 4 days after MCAO) significantly reduced the lesion of the insulted brain hemisphere and improved the neurological behavior of the rats. In primary rat hippocampal neuron cultures, treatment with NXQ at 5-20 mu g mL concentration protects the neurons against glutamate-induced excitotoxic death in a dose-dependent manner. In primary rat cerebral cortical neuron cultures, pretreatment with 5-100 mu g/mL NXQ also attenuates hypoxia-reoxygen induced neuron death and apoptosis in a dose-dependent manner. These results suggest that NXQ significantly protects the rats from MCAO ischemic injury in vivo and the hippocampal neurons from glutamate-induced excitotoxic injury as well as cortical neurons from hypoxia injury in vitro by synergistic mechanisms involving its antioxidative effects.
引用
收藏
页码:636 / 643
页数:8
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