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机构地区:[1]中国科学院上海药物研究所 [2]国家新药研究重点实验室
出 处:《中国药理学报》1998年第2期128-132,共5页Acta Pharmacologica Sinica
摘 要:目的:研究石杉碱甲对基底核大细胞部(NBM)损毁诱导的工作记忆障碍的影响.方法:采用八臂迷宫延迟插板的程序研究空间记忆.胆碱乙酰转移酶(ChAT)活力测定采用[3H]乙酰辅酶A转变成[3H]乙酰胆碱的方法.结果:单侧损毁NBM(卡因酸002μmol)导致空间记忆障碍.在不同的延迟间隔,大鼠完成程序产生的正确数减少和错误数增多.损毁侧大脑皮层ChAT酶的含量下降了大约40%.石杉碱甲(02mg·kg-1实验前30minip)改善这种空间记忆障碍.毒扁豆碱(02-03mg·kg-1实验前20minip)也有改善作用.结论:完整的NBM是空间记忆形成的关键.石杉碱甲有效的改善NBM损毁导致的空间记忆障碍.AIM: To study the effects of huperzine A on nucleus basalis magnocellularis (NBM) lesion induced spatial working memory impairment. METHODS: A delayed non match to sample radial arm maze task was used to study spatial working memory. The choline acetyltransferase (ChAT) activity was determined by the conversion of acetyl CoA to ACh . RESULTS: Unilateral NBM lesion by kainic acid 0 02 μmol impaired rats ability to perform this working memory task as evidenced by fewer correct choices after different delay intervals and more total errors to complete the task. This behavioral impairment associated with a decrease in the activity of ChAT by about 40 % in the ipsilateral cerebral cortex. Huperzine A (0 2 mg·kg -1 ip 30 min before testing) ameliorated this spatial working memory impairment. Physostigmine (0 2-0 3 mg·kg -1 ip 20 min before testing) also attenuated the NBM lesion induced memory deficit. CONCLUSION: The integrity of NBM is critical for spatial working memory processing, and this working memory impairment induced by NBM lesion can be ameliorated by huperzine A and physostigmine.
分 类 号:R749.790.5[医药卫生—神经病学与精神病学]
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