基础医学与临床 ›› 2010, Vol. 30 ›› Issue (8): 831-835.

• 研究论文 • 上一篇    下一篇

长苞凹舌兰提取物改善鹅蒿蕈氨酸致痴呆大鼠的学习记忆能力

王洁 于彩媛 张建军   

  1. 中国医学科学院北京协和医学院药物研究所 中国医学科学院北京协和医学院药物研究所 中国医学科学院北京协和医学院药物研究所
  • 收稿日期:2010-04-01 修回日期:2010-05-24 出版日期:2010-08-05 发布日期:2010-08-05
  • 通讯作者: 张建军

Improvement of Coeloglossum viride var. bracteatum extract in IBO-induced AD rats

Jie WANG, Cai-yuan YU, Jian-jun ZHANG   

  1. Institute of Material Medical, CAMS & PUMC Institute of Material Medical, CAMS & PUMC
  • Received:2010-04-01 Revised:2010-05-24 Online:2010-08-05 Published:2010-08-05
  • Contact: Jian-jun ZHANG

摘要: 目的 研究长苞凹舌兰提取物(CE)改善鹅蒿蕈氨酸(IBO)致痴呆大鼠的学习记忆能力并探讨其作用机制。方法 注射IBO (2 μl, 8 g/L) 到大鼠右侧基底前脑Meynert核(nbM),术前1h灌胃给CE,术后每日灌胃给药1次(5 mg/kg)。用Morris水迷宫与跳台实验检测学习记忆能力。Western blot检测右侧皮层、海马和纹状体的乙酰胆碱酯酶(AChE)、胆碱乙酰化酶(ChAT)、神经生长因子(NGF)及其受体酪氨酸激酶 (TrkA)的表达。结果 CE对IBO致痴呆大鼠学习记忆能力有明显的改善作用。CE使右侧nbM损伤大鼠的逃避潜伏期显著缩短。CE能够抑制右侧nbM损伤致大鼠海马AChE的过度表达。结论 CE对动物的学习记忆功能障碍有显著改善作用,抑制病理状态下AChE在海马中的过度积累可能是其作用机制之一。

Abstract: Objective To study the effect of Coeloglossum viride var. bracteatum extract (CE) on the learning and memory ability in dementia rats by ibotenic acid (IBO), and explore its mechanism. Methods IBO (2 μl, 8 g/L) was stereoscopic injected into unilateral nbM of SD rats to produce AD-mimic animal model. CE was given to rat by intragastric administration (5mg/kg) 1h before the stereoscopic operation, and after the operation once a day. The Morris water maze test and the step down test was taken. The expressions of acetylcholinesterase (AChE), choline acetyltransferase (ChAT), nerve growth factor (NGF) and tyrosine kinase (TrkA) in the hippocampus, cortex and striatum were examined by Western blot. Results CE significantly improved the learning and memory ability in IBO-induced AD-mimic rats. CE treatment shortened escape latency significantly as compared with nbM-lesion rats. The expression of AChE increased significantly in nbM-lesion rat hippocampus; CE inhibited the excessive expression of AChE. Conclusion CE could improve the dysfunction of learning and memory ability in AD animals by inhibiting the excessive expression of AChE in hippocampus under the pathological condition.