Deyo R A, Nix D A, Parker T W
Department of Psychology, Winona State University, Minnesota 55987.
Behav Neural Biol. 1992 May;57(3):260-2. doi: 10.1016/0163-1047(92)90262-3.
Reports that the dihydropyridine Ca2+ channel antagonists may facilitate memory led to the present study of the behavioral effects of nifedipine. Ninety-two 4-day-old male chicks received 0, 100 nM, 100 microM, or 10 mM nifedipine. Drugs were administered in volumes of 2 microliters into the fourth cerebral ventricle 5 min before training on a visual discrimination task. Nifedipine did not produce any detectable changes in behavior during acquisition trials. Retention, however, was impaired 24 h after training in the 100 nM and 100 microM nifedipine-treated chicks, which made significantly more errors than controls. Nifedipine did not affect the amount of time required to complete the task. No effects on body weight gain were detected, suggesting that the memory impairment was not due to a change in feeding behavior. These data are discussed in terms of the role of calcium-dependent processes in memory.
有报道称二氢吡啶类钙离子通道拮抗剂可能会促进记忆,从而引发了本项关于硝苯地平行为效应的研究。92只4日龄雄性雏鸡分别接受了0、100 nM、100 μM或10 mM的硝苯地平处理。在对视觉辨别任务进行训练前5分钟,将药物以2微升的体积注入第四脑室。在习得试验期间,硝苯地平未对行为产生任何可检测到的变化。然而,在接受100 nM和100 μM硝苯地平处理的雏鸡中,训练24小时后的记忆保持受到损害,它们比对照组犯的错误明显更多。硝苯地平不影响完成任务所需的时间。未检测到对体重增加的影响,这表明记忆损害并非由摄食行为的改变所致。本文根据钙依赖过程在记忆中的作用对这些数据进行了讨论。