中国神经再生研究(英文版) ›› 2018, Vol. 13 ›› Issue (4): 664-672.doi: 10.4103/1673-5374.230292

• 原著:脑损伤修复保护与再生 • 上一篇    下一篇

人参提取物减轻慢性脑低灌注致血管性痴呆大鼠神经元损伤及认知障碍

  

  • 收稿日期:2017-12-12 出版日期:2018-04-15 发布日期:2018-04-15
  • 基金资助:

    中国国家自然科学基金项目(81660243),贵州省科技合作项目(LG [2012] 028),贵州省科技厅项目(qian SY[2015]3041

Panax ginseng extract attenuates neuronal injury and cognitive deficits in rats with vascular dementia induced by chronic cerebral hypoperfusion

Jun-De Zhu, Jun-Jie Wang, Xian-Hu Zhang, Yan Yu, Zhao-Sheng Kang   

  1. Department of Anatomy, School of Basic Medicine, Guizhou Medical University, Guian New Area, Guizhou Province, China
  • Received:2017-12-12 Online:2018-04-15 Published:2018-04-15
  • Contact: Jun-De Zhu, jdzhu73@126.com
  • Supported by:

    This study was supported by the National Natural Science Foundation of China, No. 81660243; the Joint Foundation of Department of Science and Technology of Guizhou Province of China, No. LG [2012] 028; the Science and Technology Department of Guizhou Province of China, No. qian SY[2015]3041.

摘要:

人参是一种缓慢生长的多年生植物,其提取物具有如抗肿瘤、抗炎、抗应激等生物学活性,还对酒精致记忆力损伤大鼠有增强认知功能的作用。实验通过部分闭塞大鼠双侧颈总动脉建立血管性痴呆模型,以50或100 mg/kg的人参提取物进行灌胃治疗。实验通过Morris水迷宫和平衡木试验评估模型大鼠认知障碍,以蛋白定量试剂盒来评价胆碱能神经元水平,以免疫荧光染色检测蛋白定量试剂盒胶质纤维酸性蛋白阳性细胞数量,利用Western blot检测大脑海马CA3区中血管内皮生长因子、碱性成纤维细胞生长因子、Bcl-2和Bax表达水平。发现人参提取物灌胃治疗8周后痴呆大鼠的认知障碍明显改善,大脑胆碱能神经元数量明显提升,大脑海马CA3区的神经递质血管内皮生长因子和碱性成纤维细胞生长因子表达增加,胶质纤维酸性蛋白阳性细胞数量减少,还通过上调Bcl-2表达并下调Bax表达抑制了神经元的凋亡;且人参提取物的作用呈剂量依赖性,效果与临床常用的治疗血管性痴呆的药物尼莫地平接近。表明人参提取物对慢性缺血致血管性痴呆具有神经保护作用,可能成为预防及治疗血管性痴呆的有效药物。

orcid:0000-0001-9666-8010(Jun-De Zhu )

关键词: 神经再生, 人参提取物, 慢性缺血, 血管性痴呆, 学习记忆能力, 血管内皮生长因子, 碱性成纤维细胞生长因子, 细胞凋亡

Abstract:

Panax ginseng is a slow-growing perennial plant. Panax ginseng extract has numerous biological activities, including antitumor, anti-inflammatory and antistress activities. Panax ginseng extract also has a cognition-enhancing effect in rats with alcohol-induced memory impairment. In this study, we partially occluded the bilateral carotid arteries in the rat to induce chronic cerebral hypoperfusion, a wellknown model of vascular dementia. The rats were then intragastrically administered 50 or 100 mg/kg Panax ginseng extract. Morris water maze and balance beam tests were used to evaluate memory deficits and motor function, respectively. Protein quantity was used to evaluate cholinergic neurons. Immunofluorescence staining was used to assess the number of glial fibrillary acidic protein-positive cells.Western blot assay was used to evaluate protein levels of vascular endothelial growth factor, basic fibroblast growth factor, Bcl-2 and Bax.Treatment with Panax ginseng extract for 8 weeks significantly improved behavioral function and increased neuronal density and VEGF and bFGF protein expression in the hippocampal CA3 area. Furthermore, Panax ginseng extract reduced the number of glial fibrillary acidic protein-immunoreactive cells, and it decreased apoptosis by upregulating Bcl-2 and downregulating Bax protein expression. The effect of Panax ginseng extract was dose-dependent and similar to that of nimodipine, a commonly used drug for the treatment of vascular dementia. These findings suggest that Panax ginseng extract is neuroprotective against vascular dementia induced by chronic cerebral hypoperfusion,and therefore might have therapeutic potential for preventing and treating the disease.

Key words: nerve regeneration, Panax ginseng extract, chronic cerebral hypoperfusion, vascular dementia, learning and memory, vascular endothelial growth factor, basic fibroblast growth factor, apoptosis, neural regenerat