Dourish C T, Hutson P H, Curzon G
Psychopharmacology (Berl). 1986;89(4):467-71. doi: 10.1007/BF02412123.
The effects of para-chlorophenylalanine pre-treatment (PCPA, 150 mg/kg IP daily for 3 days) on feeding and stereotyped behaviour elicited by the serotonin agonist 8-hydroxy-2-(di-n-propylamino) tetralin (8-OH-DPAT) in rats were investigated. PCPA depleted brain serotonin and 5-hydroxyindoleacetic acid concentrations by 90% and increased feeding during a 2-h day-time test. 8-OH-DPAT (60-4000 micrograms/kg SC) increased food intake in control animals but decreased it in PCPA-treated animals during the 2-h test. PCPA treatment had no effect on 8-OH-DPAT-induced locomotion or serotonin-related stereotyped behaviour (i.e. forepaw treading, headweaving, wet dog shakes, etc). Since PCPA prevents the operation of pre-synaptic serotonergic mechanisms, the failure of 8-OH-DPAT to increase food intake in PCPA-treated rats suggests that 8-OH-DPAT-induced hyperphagia is autoreceptor mediated.
研究了对氯苯丙氨酸预处理(PCPA,每日腹腔注射150mg/kg,持续3天)对大鼠中血清素激动剂8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT)引发的进食和刻板行为的影响。PCPA使脑血清素和5-羟基吲哚乙酸浓度降低90%,并在2小时的白天测试中增加进食量。在2小时的测试中,8-OH-DPAT(60-4000微克/千克皮下注射)增加了对照动物的食物摄入量,但减少了PCPA处理动物的食物摄入量。PCPA处理对8-OH-DPAT诱导的运动或血清素相关的刻板行为(即前爪踩踏、头部摆动、湿狗抖等)没有影响。由于PCPA阻止了突触前血清素能机制的运作,8-OH-DPAT在PCPA处理的大鼠中未能增加食物摄入量,这表明8-OH-DPAT诱导的摄食过多是由自身受体介导的。