Nakagawa Y, Iwasaki T
Tsukuba Research Laboratories, Experimental Biomedical Research Inc. (Jisseiken), Ibaraki, Japan.
Brain Res. 1996 Jan 15;706(2):227-32. doi: 10.1016/0006-8993(95)01040-8.
Involvement of N-methyl-D-aspartate (NMDA) receptor complex and 5-hydroxytryptamine3 (5-HT3) receptors in state-dependent learning (SDL) induced by ethanol (EtOH) was investigated in the step-through passive avoidance task in rats. Pre-training injections of EtOH or MK-801 reduced step-through latency in the test session conducted 24 h after the training session. Pre-test as well as pre-training injections of EtOH failed to reduce the latency, while pre-training and pre-test injections of MK-801 reduced the latency. These results show that EtOH but not MK-801 produces SDL. SDL induced by EtOH was blocked by ICS205-930 injected before either the training or test session. However, ICS205-930 failed to block SDL induced by diazepam and muscimol. These results suggest that NMDA receptor complex may not be involved in SDL, and that 5-HT3 receptors may contribute to SDL induced by EtOH but not by diazepam and muscimol.
在大鼠的穿梭箱被动回避任务中,研究了N-甲基-D-天冬氨酸(NMDA)受体复合物和5-羟色胺3(5-HT3)受体在乙醇(EtOH)诱导的状态依赖性学习(SDL)中的作用。在训练 session 后24小时进行的测试 session 中,训练前注射EtOH或MK-801可缩短穿梭潜伏期。训练前以及测试前注射EtOH未能缩短潜伏期,而训练前和测试前注射MK-801可缩短潜伏期。这些结果表明,是EtOH而非MK-801产生了SDL。在训练或测试 session 之前注射ICS205-930可阻断EtOH诱导的SDL。然而,ICS205-930未能阻断地西泮和蝇蕈醇诱导的SDL。这些结果表明,NMDA受体复合物可能不参与SDL,并且5-HT3受体可能促成了EtOH而非地西泮和蝇蕈醇诱导的SDL。