Growdon J H
Neurology. 1977 Nov;27(11):1074-7. doi: 10.1212/wnl.27.11.1074.
A single dose of p-chloroamphetamine, 10 mg per kilogram, produced postural abnormalities, tremor, myoclonus, and autonomic signs in rats 5 minutes after intraperitoneal injection. This syndrome lasted 60 to 90 minutes, and its intensity was directly proportional to the amount of p-chloroamphetamine given over a 2 to 10 mg per kilogram range. Whole-brain levels of serotonin and 5-hydroxyindoleacetic acid were not altered during this interval, although both were reduced significantly 1 day later. Pretreatment with drugs that interfere with the uptake of p-chloroamphetamine into terminals of serotonergic neurons (fluoxetine), depress brain serotonin levels (p-chlorophenylalanine), or block serotonin receptors (methiothepin or methergoline) suppressed this syndrome, whereas drugs that antagonize the effects of dopamine, norepinephrine, and acetylcholine did not. These observations implicate serotonergic mechanisms and provide behavioral evidence of p-chloroamphetamine's immediate actions on serotonergic neurons in the central nervous system.
腹腔注射10毫克/千克的对氯苯丙胺单剂量后5分钟,大鼠出现姿势异常、震颤、肌阵挛和自主神经体征。该综合征持续60至90分钟,其强度与2至10毫克/千克范围内给予的对氯苯丙胺量成正比。在此期间,全脑血清素和5-羟吲哚乙酸水平未发生改变,尽管1天后两者均显著降低。用干扰对氯苯丙胺摄取到血清素能神经元终末的药物(氟西汀)、降低脑血清素水平的药物(对氯苯丙氨酸)或阻断血清素受体的药物(甲硫噻嗪或麦角新碱)进行预处理可抑制该综合征,而拮抗多巴胺、去甲肾上腺素和乙酰胆碱作用的药物则不能。这些观察结果表明血清素能机制参与其中,并提供了对氯苯丙胺对中枢神经系统血清素能神经元直接作用的行为证据。