Zarrindast Mohammad Reza, Misaghi Sara, Ahmadi Shamseddin
Department of Pharmacology, School of Medicine and Iranian National Center for Addiction Studies, Tehran University of Medical Sciences, Tehran, Iran.
Eur J Pharmacol. 2008 Aug 20;590(1-3):198-203. doi: 10.1016/j.ejphar.2008.06.009. Epub 2008 Jun 7.
The effects of dopaminergic drugs on the inhibitory avoidance memory affected by lithium were examined in the Naval Medical Research Institute (NMRI) mice using a single-trial step-down inhibitory (passive) avoidance task. The results showed that post-training administration of lithium (10 mg/kg, i.p.) decreased the step-down latency on the test day, which was fully or partly reversed by pre-test administration of the same dose of the drug; suggesting state-dependent learning induced by lithium. Our results also showed that pre-test (i.p.) administration of the dopamine D1 receptor agonist SKF38393 and the dopamine D2 receptor agonist quinpirole by themselves and in combination with ineffective doses of lithium (0.3, 0.6 and 1.25 mg/kg) reversed the decrease of the step-down latency induced by post-training lithium. In contrast, pre-test administration of the dopamine D1 receptor antagonist SCH23390 (0.025, 0.05 and 0.1 mg/kg, i.p.) and the dopamine D2 receptor antagonist sulpiride (6.25 and 12.5 mg/kg, i.p.) alone or in combination with pre-test lithium (10 mg/kg), did not significantly alter the step-down latency on the test day, except for a higher dose of sulpiride (25 mg/kg) which by itself increased the step-down latency. Furthermore, pre-test administration of a lower dose of sulpiride (3 mg/kg) in combination with ineffective doses of lithium (03, 0.6 and 1.25 mg/kg) also reversed the decrease in the step-down latency induced by post-training lithium. In conclusion, the dopamine D1 and D2 receptor mechanism(s) may be involved, at least partly, in the effect of lithium on retrieval of the inhibitory avoidance memory influenced by the drug.
使用单次递减抑制(被动)回避任务,在海军医学研究所(NMRI)小鼠中研究了多巴胺能药物对受锂影响的抑制性回避记忆的作用。结果表明,训练后给予锂(10毫克/千克,腹腔注射)可缩短测试日的递减潜伏期,而在测试前给予相同剂量的药物可完全或部分逆转这一现象;这表明锂诱导了状态依赖性学习。我们的结果还表明,在测试前腹腔注射多巴胺D1受体激动剂SKF38393和多巴胺D2受体激动剂喹吡罗,以及它们与无效剂量的锂(0.3、0.6和1.25毫克/千克)联合使用,均可逆转训练后锂诱导的递减潜伏期缩短。相比之下,在测试前腹腔注射多巴胺D1受体拮抗剂SCH23390(0.025、0.05和0.1毫克/千克)和多巴胺D2受体拮抗剂舒必利(6.25和12.5毫克/千克),单独或与测试前锂(10毫克/千克)联合使用时,除了较高剂量的舒必利(25毫克/千克)本身可增加递减潜伏期外,并未显著改变测试日的递减潜伏期。此外,在测试前给予较低剂量的舒必利(3毫克/千克)与无效剂量的锂(0.3、0.6和1.25毫克/千克)联合使用,也可逆转训练后锂诱导的递减潜伏期缩短。总之,多巴胺D1和D2受体机制可能至少部分参与了锂对受该药物影响的抑制性回避记忆恢复的作用。