Khodayar Ebrahim, Oryan Shahrbanoo, Nasehi Mohammad, Zarrindast Mohammad-Reza
aDepartment of Biology, Faculty of Basic Sciences, Kharazmi (Tarbiat Moalem) University bCognitive and Neuroscience Research Center (CNRC), Medical Genomics Research Center and School of Advanced Sciences in Medicine, Islamic Azad University, Tehran Medical Sciences Branch cDepartment of Pharmacology, School of Medicine dIranian National Center for Addiction Studies, Tehran University of Medical Sciences eSchool of Cognitive Sciences, Institute for Research in Fundamental Sciences (IPM), Tehran, Iran.
Behav Pharmacol. 2016 Feb;27(1):12-21. doi: 10.1097/FBP.0000000000000174.
The present study investigates the effects of 5-HT4 receptors of the nucleus accumbens (NAc) shell on the impairment of emotional memory consolidation induced by cannabinoid CB1 receptor stimulation. The elevated plus maze test-retest paradigm was used to assess memory in adult male Wistar rats. Intra-NAc shell administration of ACPA (selective cannabinoid CB1 receptor agonist 0.006 µg/rat) and RS23597 (5-HT4 receptor antagonist 0.01 µg/rat), immediately after training, decreased emotional memory consolidation, suggesting a drug-induced amnesia, whereas post-training intra-NAc shell microinjections of RS67333 (5-HT4 receptor agonist 0.016 µg/rat) increased emotional memory consolidation. Interestingly, RS67333 exerted a dual effect on ACPA-induced behaviors, potentiating and restoring amnesia caused by the subthreshold and effective doses of ACPA, respectively. However, neither RS23597 nor AM251 (CB1 receptor antagonist 30, 60 and 120 ng/rat) affected emotional memory consolidation. Nonetheless, a subthreshold dose of AM251 (120 ng/rat) reversed the amnesia induced by ACPA (0.006 µg/rat) and RS23597 (0.01 µg/rat). None of the above doses altered the locomotor activity. In conclusion, our results suggest that the NAc-shell 5-HT4 receptors are involved in the modulation of ACPA-induced amnesia.
本研究调查伏隔核(NAc)壳部5-羟色胺4(5-HT4)受体对大麻素CB1受体刺激诱导的情绪记忆巩固损伤的影响。采用高架十字迷宫重测范式评估成年雄性Wistar大鼠的记忆。训练后立即向NAc壳部注射ACPA(选择性大麻素CB1受体激动剂0.006μg/只大鼠)和RS23597(5-HT4受体拮抗剂0.01μg/只大鼠),会降低情绪记忆巩固,提示药物诱导的失忆,而训练后向NAc壳部微量注射RS67333(5-HT4受体激动剂0.016μg/只大鼠)则会增强情绪记忆巩固。有趣的是,RS67333对ACPA诱导的行为产生双重作用,分别增强和恢复了亚阈值剂量和有效剂量ACPA引起的失忆。然而,RS23597和AM251(CB1受体拮抗剂30、60和120ng/只大鼠)均未影响情绪记忆巩固。尽管如此,亚阈值剂量的AM251(120ng/只大鼠)可逆转ACPA(0.006μg/只大鼠)和RS23597(0.01μg/只大鼠)诱导的失忆。上述剂量均未改变运动活性。总之,我们的结果表明,NAc壳部的5-HT4受体参与了ACPA诱导的失忆调节。