Kotlińska J, Biała G
Department of Pharmacodynamics, Medical University School, Lublin, Poland.
Pol J Pharmacol. 2000 May-Jun;52(3):179-85.
The influence of uncompetitive NMDA receptor antagonist, 1-amino-3,5--dimethyl-adamantane (memantine) and partial glycineB site agonist, 1-amino-cyclopropanecarboxylic acid (ACPC) on cocaine-induced conditioned place preference (CPP) were examined in male Wistar rats. After determination of initial preference, animals were conditioned with cocaine (5 mg/kg, ip) for 3 conditioning trials, alone or in combination with memantine (7.5 mg/kg, ip) or ACPC (50.0 mg/kg, ip). Memantine prevented acquisition and expression of the place preference produced by cocaine, while ACPC prevented only acquisition effect. Neither of the NMDA antagonists displayed any reinforcing properties by itself. Our current data suggest that the NMDA receptor complex may be involved in the rewarding effect of cocaine.
在雄性Wistar大鼠中,研究了非竞争性N-甲基-D-天冬氨酸(NMDA)受体拮抗剂1-氨基-3,5-二甲基金刚烷(美金刚)和部分甘氨酸B位点激动剂1-氨基环丙烷羧酸(ACPC)对可卡因诱导的条件性位置偏爱(CPP)的影响。在确定初始偏爱后,动物接受可卡因(5mg/kg,腹腔注射)单独或与美金刚(7.5mg/kg,腹腔注射)或ACPC(50.0mg/kg,腹腔注射)联合进行3次条件性试验。美金刚可阻止可卡因产生的位置偏爱的获得和表达,而ACPC仅阻止获得效应。两种NMDA拮抗剂自身均未表现出任何强化特性。我们目前的数据表明,NMDA受体复合物可能参与了可卡因的奖赏效应。