Wass Caroline, Archer Trevor, Pålsson Erik, Fejgin Kim, Alexandersson Asa, Klamer Daniel, Engel Jörgen A, Svensson Lennart
Department of Pharmacology, The Sahlgrenska Academy at Göteborg University, POB 431, SE 405 30 Göteborg, Sweden.
Behav Brain Res. 2006 Nov 1;174(1):49-55. doi: 10.1016/j.bbr.2006.07.003. Epub 2006 Aug 28.
Phencyclidine (PCP), a non-competitive NMDA receptor antagonist, was used to model schizophrenia-like cognitive dysfunctions of learning and memory in rats using the Morris water maze model for spatial memory. A protocol introduced by Baldi and co-workers was used to distinguish working memory from reference memory. Male Sprague-Dawley rats were administered PCP (2.0 mg/kg) before the first swimming trial on each of five spatial memory acquisition days, either alone or after pre-treatment with the nitric oxide synthase inhibitor, L-NAME (10 mg/kg). Probe tests for memory were conducted before and after each acquisition session. The results showed that PCP disrupted the acquisition of both working and reference memory. Pre-treatment with L-NAME reversed both these effects of PCP. L-NAME treatment by itself did not significantly alter either acquisition or retention of spatial memory.
苯环己哌啶(PCP)是一种非竞争性N-甲基-D-天冬氨酸(NMDA)受体拮抗剂,利用莫里斯水迷宫模型来模拟大鼠学习和记忆方面类似精神分裂症的认知功能障碍,该模型用于空间记忆研究。采用由巴尔迪及其同事提出的实验方案来区分工作记忆和参考记忆。在五个空间记忆获取日中的每个第一天游泳试验前,给雄性斯普拉格-道利大鼠单独注射PCP(2.0毫克/千克),或者在一氧化氮合酶抑制剂L- NAME(10毫克/千克)预处理后注射PCP。在每次获取训练前后进行记忆探针测试。结果表明,PCP破坏了工作记忆和参考记忆的获取。用L- NAME预处理可逆转PCP的这两种作用。单独使用L- NAME处理对空间记忆的获取或保持均无显著影响。