Protective effect of extract of Acanthopanax senticosus harms on dopaminergic neurons in Parkinson's disease mice

Protective effect of extract of Acanthopanax senticosus harms on dopaminergic neurons in Parkinson's disease mice
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刺五加提取物对帕金森病小鼠多巴胺能神经元损伤的保护作用

DOI:
10.1016/j.phymed.2012.02.006
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发表时间:
2012-05-15
期刊:
影响因子:
7.9
通讯作者:
Lu, Fang
Lu, Fang
中科院分区:
医学1区
文献类型:
--
作者:
Liu, Shu-min;Li, Xu-zhao;Lu, Fang

文献摘要

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To study the neuroprotective effect of extract of Acanthopanax senticosus Harms against MPTP-induced mice model of Parkinson's disease and its mechanism. The Parkinson's disease mice model was induced by 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine Hydrochloride (MPTP-HCl, 30 mg/kg daily for 5 days). High dose group and low dose group were medicated with extract of Acanthopanax senticosus Harms for 20 days, dose amounted to 182 mg/kg and 45.5 mg/kg daily respectively. The behavioral testing of mice was assessed using pole-climbing test. The levels of Dopamine (DA) and Homovanillic acid (HVA) in striatum were determined by Ultra-performance liquid chromatography combined with time-of-flight mass spectrometry (UPLC-ToF-MS). The levels of dopamine receptor 1 and 2 in striatum were assayed simultaneously with the help of immunohistochemical method. The level of Caspase-3 protein in substantia nigra was analyzed by Western Blot. From Day 5 during the administration of extract of Acanthopanax senticosus Harms, pole-climbing time in low and high dose group were significantly less than model group (p < 0.05). Compared with model group, the DA level of striatum in low dose group was significantly higher (p < 0.01), the number of dopamine receptor 1 and dopamine receptor 2-positive cells in low and high dose group were significantly less (p < 0.05), the Caspase-3 protein level of substantia nigra in low and high dose group were significantly less (p < 0.05). The neuroprotective effect of extract of Acanthopanax senticosus Harms may be able to protect C57BL/6 mice against MPTP-induced dopaminergic neuronal damage. (C) 2012 Elsevier GmbH. All rights reserved.