Whishaw I Q
Behav Neurosci. 1985 Oct;99(5):979-1005. doi: 10.1037//0735-7044.99.5.979.
Normal rats and rats drugged with atropine sulfate, a cholinergic muscarinic blocker, were evaluated in the Morris water task for their use of spatial navigation strategies. Atropine-treated rats were impaired on a place response of swimming to a platform hidden in a pool filled with opaque water. With extended training, they did learn the place response, though not with control precision, as shown by better than chance heading angles upon swim initiation, searches in the old location for a platform that had been moved, and by correct swims from novel starting locations. Acquisition could not be accounted for by habituation to the drug. In contrast with the acquisition deficit, pretrained rats were relatively unimpaired by the drug. In separate experiments, the strategies used by the drugged animals were examined. Atropine-treated rats were not impaired in acquisition or retention of a cue task, swimming to a visible platform, or a position response task, turning left to locate a platform, but both control and atropine-treated rats were unable to reverse position responses. Possibly, atropine-treated rats can use cue and position response strategies in part or in combination to acquire a place response. Atropine-treated rats were unable to acquire a place learning set, which involved swimming to a new location each day, a response that is eventually performed by normal rats in approximately one trial. They also were unable to perform a learning-set response, which they had acquired when undrugged. Insofar as the impairments following atropine are characteristic of a deficit in the use of a locale strategy, that is, making rapid use of relational properties of distal cues, whereas their successes are characteristic of the use of taxon strategies, that is, cue or position responses, the results suggest that locale systems of navigation are more importantly dependent on cholinergic brain mechanisms than taxon strategies. The resistance of preacquired place responses to atropine may suggest that normally rats acquire place responses by using a locale strategy but effect rehearsed responses by using taxon strategies. Finally, characteristic differences in acquisition, retention, and reversal of atropine-treated and control rats using different navigational strategies suggest new possibilities for interpreting various performance features displayed by animals after other types of treatment.
在莫里斯水迷宫任务中,对正常大鼠以及用硫酸阿托品(一种胆碱能毒蕈碱受体阻滞剂)麻醉的大鼠运用空间导航策略的情况进行了评估。经阿托品处理的大鼠在游向隐藏于充满不透明水的水池中的平台的位置反应方面存在缺陷。经过长时间训练,它们确实学会了位置反应,尽管不如对照组精准,这表现为游泳开始时航向角度优于随机水平、在平台已移动的旧位置进行搜索,以及从新的起始位置正确游向平台。习得过程不能用对药物的适应来解释。与习得缺陷形成对比的是,经过预训练的大鼠受药物影响相对较小。在单独的实验中,研究了经药物处理的动物所采用的策略。经阿托品处理的大鼠在习得或保留线索任务(游向可见平台)或位置反应任务(向左转以找到平台)方面没有缺陷,但对照组和经阿托品处理的大鼠都无法反转位置反应。可能的情况是,经阿托品处理的大鼠可以部分地或联合使用线索和位置反应策略来习得位置反应。经阿托品处理的大鼠无法习得位置学习集,该学习集要求每天游向一个新位置,而正常大鼠最终大约在一次试验中就能完成这个反应。它们也无法做出在未用药时习得的学习集反应。鉴于阿托品处理后的损伤是使用场所策略(即快速利用远处线索的关系属性)存在缺陷的特征,而它们的成功是使用分类策略(即线索或位置反应)的特征,结果表明,与分类策略相比,场所导航系统更重要地依赖于胆碱能脑机制。预先习得的位置反应对阿托品的抗性可能表明,正常情况下大鼠通过使用场所策略习得位置反应,但通过使用分类策略来实现熟练反应。最后,经阿托品处理的大鼠和对照组大鼠在使用不同导航策略时,在习得、保留和反转方面的特征差异为解释动物在其他类型处理后表现出的各种行为特征提供了新的可能性。