Bradbury A J, Costall B, Naylor R J, Onaivi E S
Postgraduate School of Studies in Pharmacology, University of Bradford, UK.
Psychopharmacology (Berl). 1987;93(4):457-65. doi: 10.1007/BF00207235.
d-Amphetamine, in doses lower than required to increase motor activity, reduced mouse spontaneous locomotor activity when this was assessed using cages equipped with photocell units, using treadwheels, or the measurement of spontaneous climbing behaviour. Acute treatments with the serotonergic agonists quipazine and 5-hydroxy-DL-tryptophan also reduced wheel running activity, spontaneous locomotor activity assessed using photocell cages, and spontaneous climbing behaviour; fenfluramine caused a similar effect. Pretreatment with 5-hydroxy-DL-tryptophan enhanced the inhibitory effects of d-amphetamine. A 3-day treatment with fenfluramine, or lesions of the median raphe nucleus (but not the dorsal raphe nucleus) abolished the ability of d-amphetamine to reduce motor activity in the three test systems. It is concluded that low doses of d-amphetamine can reduce locomotor activity and that the effects may be mediated via an enhancement of the release of 5-hydroxytryptamine from the system arising in the median raphe nucleus.
右旋苯丙胺在低于增加运动活性所需剂量时,当使用配备光电管装置的笼子、跑步机或测量自发攀爬行为来评估时,会降低小鼠的自发运动活性。用血清素能激动剂喹哌嗪和5-羟基-DL-色氨酸进行急性处理也会降低跑步轮活动、使用光电管笼子评估的自发运动活性以及自发攀爬行为;芬氟拉明也有类似作用。用5-羟基-DL-色氨酸预处理可增强右旋苯丙胺的抑制作用。用芬氟拉明进行为期3天的处理,或中缝正中核(而非中缝背核)损伤会消除右旋苯丙胺在这三种测试系统中降低运动活性的能力。结论是低剂量的右旋苯丙胺可降低运动活性,且这些作用可能通过增强从中缝正中核产生的系统中5-羟色胺的释放来介导。