Connor D J, Langdon D J, Langlais P J, Thal L J
Department of Neurosciences, University of California, San Diego, La Jolla 92093.
Neurobiol Aging. 1993 Nov-Dec;14(6):535-7. doi: 10.1016/0197-4580(93)90036-b.
Fisher 344 rats underwent bilateral nucleus basalis magnocellularis (NBm) lesioning followed by testing in a delayed nonmatching-to-sample T-maze task. Both lesion and control animals acquired the task although the NBm animals were mildly impaired on acquisition and on trials to criterion. Increasing the delay reduced accuracy of performance equally in both groups. The NBm lesion did not alter the level of several thalamic amino acids. These data indicate that NBm lesioning does not produce a significant impairment in working or reference memory in this task and supports the hypothesis that NBm lesioning impairs attention.
对费希尔344大鼠进行双侧大细胞基底核(NBm)损伤,随后在延迟非匹配样本T迷宫任务中进行测试。尽管NBm损伤组的大鼠在任务习得和达到标准的试验中受到轻度损害,但损伤组和对照组动物均学会了该任务。增加延迟会使两组动物的表现准确性同等程度降低。NBm损伤并未改变几种丘脑氨基酸的水平。这些数据表明,NBm损伤在该任务中不会对工作记忆或参考记忆产生显著损害,并支持NBm损伤会损害注意力这一假设。