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大鼠大细胞基底核注射鹅膏蕈氨酸后的记忆障碍

Memory disturbances following ibotenic acid injections in the nucleus basalis magnocellularis of the rat.

作者信息

Mayo W, Kharouby M, Le Moal M, Simon H

机构信息

INSERM U. 259, Université de Bordeaux II, France.

出版信息

Brain Res. 1988 Jul 12;455(2):213-22. doi: 10.1016/0006-8993(88)90079-0.

Abstract

The behavioral effects of lesions of the nucleus basalis magnocellularis (NBM) on two spatial discrimination tasks (place navigation and cross maze) were examined in the rat. These tasks were designed to test reference memory. Lesions by bilateral injection of ibotenic acid into the NBM led to a severe and permanent impairment in the learning of the cross maze task. In the learning of the place navigation task, the rats with lesions showed only a transient deficit. Immediately after the removal of the platform, the rats with lesions explored the quadrant (NE) previously containing the platform as long as controls and above chance levels. The rats with lesions did not extinguish exploration like the controls, seen as a reduction both in time spent in the NE quadrant and in swimming activity. Taken together, the results showed that (1) NBM lesions impair reference memory, but (2) spare other aspects of memory. On the basis of the results in the place navigation task, procedural memory was assumed to remain intact after lesion of the NBM. Biochemical assays of choline acetyltransferase (ChAT) in various brain regions in the lesioned animals demonstrated a reduced ChAT activity in the neocortical projections of the NBM but not in the hippocampus. However, it cannot be decided from this work whether behavioral deficits result from the lesion of cholinergic or of non-cholinergic cells in the NBM.

摘要

在大鼠中研究了基底大细胞核(NBM)损伤对两种空间辨别任务(位置导航和十字迷宫)的行为影响。这些任务旨在测试参考记忆。通过向NBM双侧注射鹅膏蕈氨酸造成的损伤导致十字迷宫任务学习中出现严重且永久性的损害。在位置导航任务的学习中,损伤大鼠仅表现出短暂的缺陷。移除平台后,损伤大鼠对先前放置平台的象限(东北象限)的探索时间与对照组相同且高于随机水平。损伤大鼠不像对照组那样停止探索,表现为在东北象限花费的时间和游泳活动均减少。综合来看,结果表明:(1)NBM损伤会损害参考记忆,但(2)不影响记忆的其他方面。根据位置导航任务的结果,推测NBM损伤后程序性记忆仍保持完整。对损伤动物不同脑区的胆碱乙酰转移酶(ChAT)进行生化分析表明,NBM的新皮质投射中ChAT活性降低,但海马体中未降低。然而,从这项研究尚无法确定行为缺陷是由NBM中胆碱能细胞还是非胆碱能细胞的损伤导致的。

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