Mélan C, Eichenlaub D, Ungerer A, Messier C, Destrade C
Laboratoire de Psychophysiologie, Université Louis Pasteur, URA 1295 CNRS, Strasbourg, France.
Pharmacol Biochem Behav. 1997 Apr;56(4):589-94. doi: 10.1016/s0091-3057(96)00404-2.
We investigated the effects of immediate post-training systemic administration of gamma-L-glutamyl-L-aspartate (gamma-LGLA) and 3-(2-carboxypiperazine-4-yl)-propyl-1-phosphonate (CPP), antagonists at the N-methyl-D-aspartate receptor, in a lever-press task in two inbred strains of mice. When retention performance was tested in control animals 24 h after partial acquisition of the task. BALB/c mice exhibited a spontaneous performance improvement whereas C57BL/6J mice did not gamma-LGLA at doses of 2.5 and 25 mumol/kg and CPP at doses ranging between 0.025 and 2.5 mumol/kg blocked the spontaneous performance improvement found in BALB/c mice but had no apparent effects on the retention performance of C57BL/6J mice. These data suggest that retention impairment induced by CPP and gamma-LGLA in BALB/c mice results from an interference with posttraining memory processes.
我们研究了在两种近交系小鼠的杠杆按压任务中,训练后立即全身给予N-甲基-D-天冬氨酸受体拮抗剂γ-L-谷氨酰-L-天冬氨酸(γ-LGLA)和3-(2-羧基哌嗪-4-基)-丙基-1-膦酸酯(CPP)的效果。当在部分习得任务24小时后对对照动物进行记忆保持测试时,BALB/c小鼠表现出自发性的成绩提高,而C57BL/6J小鼠则没有。剂量为2.5和25 μmol/kg的γ-LGLA以及剂量在0.025至2.5 μmol/kg之间的CPP可阻断BALB/c小鼠中发现的自发性成绩提高,但对C57BL/6J小鼠的记忆保持成绩没有明显影响。这些数据表明,CPP和γ-LGLA在BALB/c小鼠中诱导的记忆保持损伤是由于干扰了训练后的记忆过程。