Santucci A C, Knott P J, Haroutunian V
Psychiatry Service, Bronx VA Medical Center, NY 10468, USA.
Eur J Pharmacol. 1996 Jan 4;295(1):7-17. doi: 10.1016/0014-2999(95)00629-x.
Eight experiments compared and contrasted the effects of serotonin release and depletion on performance by rats in two tests of memory. Most experiments (Experiments 1-5) examined the effects of the serotonergic releasing/depleting agent p-chloroamphetamine on passive avoidance performance. Additional experiments explored p-chloroamphetamine's effects on retention performance by animals trained in an 8-arm radial maze (Experiment 6), and the effects of dorsal raphe nucleus lesions on passive avoidance in animals treated with (Experiment 8) or not treated with (Experiment 7) p-chloroamphetamine. In general, acute increases in serotonin release produced consistent and extensive retention performance deficits in both passive avoidance and radial arm maze. Results from an ancillary control experiment indicated that the p-chloroamphetamine-induced passive avoidance impairment was not related to drug-induced alterations in pain sensitivity. Other experiments ruled out the possibility that p-chloroamphetamine was disrupting passive avoidance retention performance by affecting post-trial consolidation processes, producing state-dependent retention, having direct effects at postsynaptic receptors, or indirectly by affecting non-serotonergic neurotransmitter systems. Depletion of serotonin resulting from either the long-term residual effects of p-chloroamphetamine or lesions of the dorsal raphe nucleus failed to alter passive avoidance retention scores although it produced extensive depletion (45-85%) of serotonin and 5-hydroxyindoleacetic acid in the cortex and hippocampus. These data contribute to the growing body of literature indicating an important role of serotonin in cognitive processes by demonstrating that excessive release, but not depletion, of serotonin produces profound retention performance impairment.
八项实验比较并对比了血清素释放和耗竭对大鼠在两项记忆测试中表现的影响。大多数实验(实验1 - 5)研究了血清素释放/耗竭剂对氯苯丙胺对被动回避表现的影响。额外的实验探讨了对氯苯丙胺对在八臂放射状迷宫中训练的动物的记忆保持表现的影响(实验6),以及中缝背核损伤对用(实验8)或未用(实验7)对氯苯丙胺处理的动物的被动回避的影响。总体而言,血清素释放的急性增加在被动回避和放射状迷宫实验中均产生了一致且广泛的记忆保持表现缺陷。一项辅助对照实验的结果表明,对氯苯丙胺引起的被动回避损伤与药物引起的痛觉敏感性改变无关。其他实验排除了对氯苯丙胺通过影响试验后巩固过程、产生状态依赖性记忆、直接作用于突触后受体或间接影响非血清素能神经递质系统来破坏被动回避记忆保持表现的可能性。尽管对氯苯丙胺的长期残留效应或中缝背核损伤导致血清素耗竭,使皮质和海马中的血清素和5 - 羟吲哚乙酸大量耗竭(45 - 85%),但并未改变被动回避记忆保持分数。这些数据通过证明血清素的过度释放而非耗竭会导致严重的记忆保持表现损伤,为越来越多表明血清素在认知过程中起重要作用的文献做出了贡献。