Samuels E R, Hou R H, Langley R W, Szabadi E, Bradshaw C M
Psychopharmacology Section, Division of Psychiatry, University of Nottingham, Nottingham, UK.
J Psychopharmacol. 2006 Nov;20(6):756-70. doi: 10.1177/0269881106060770. Epub 2006 Jan 9.
The noradrenergic locus coeruleus is a major wakefulness-promoting nucleus of the brain, which is also involved in the regulation of autonomic and endocrine functions. The activity of the locus coeruleus is believed to be tonically enhanced by a mesocoerulear dopaminergic pathway arising from the ventral tegmental area of the midbrain. Both modafinil, a wakefulness-promoting drug, and pramipexole, a D(2)/D(3)receptor agonist with sedative properties, may act on this pathway, with modafinil increasing and pramipexole decreasing locus coeruleus activity. The aim of this study was to compare the two drugs on alertness, autonomic and endocrine functions in healthy volunteers. Pramipexole (0.5mg), modafinil (200mg), and their combination were administered to 16 healthy males in a double-blind, placebo-controlled design. Methods included tests of alertness (pupillographic sleepiness test, critical flicker fusion frequency, visual analogue scales), autonomic functions (resting pupil diameter, light and darkness reflex responses, heart rate, blood pressure, salivation, core temperature), and endocrine functions (blood concentrations of prolactin, growth hormone, and thyroid stimulating hormone). Data were analysed by ANOVA. Pramipexole reduced alertness, caused pupil dilatation, increased heart rate, reduced prolactin and thyroid stimulating hormone, and increased growth hormone level. Modafinil caused small increases in blood pressure and core temperature, and reduced prolactin levels. The sedative effect of pramipexole and the autonomic effects of modafinil are consistent with altered activity in the mesocoerulear pathway; the pupil dilatation following pramipexole suggests reduced dopaminergic excitation of the Edinger-Westphal nucleus.
去甲肾上腺素能蓝斑核是大脑中促进觉醒的主要核团,也参与自主神经和内分泌功能的调节。蓝斑核的活动被认为受到一条从中脑腹侧被盖区发出的中脑蓝斑多巴胺能通路的紧张性增强作用。促觉醒药物莫达非尼和具有镇静特性的D(2)/D(3)受体激动剂普拉克索都可能作用于这条通路,莫达非尼增加而普拉克索降低蓝斑核的活动。本研究的目的是比较这两种药物对健康志愿者的警觉性、自主神经和内分泌功能的影响。采用双盲、安慰剂对照设计,将普拉克索(0.5mg)、莫达非尼(200mg)及其组合给予16名健康男性。方法包括警觉性测试(瞳孔描记法嗜睡测试、临界闪烁融合频率、视觉模拟量表)、自主神经功能(静息瞳孔直径、明暗反射反应、心率、血压、唾液分泌、核心体温)和内分泌功能(催乳素、生长激素和促甲状腺激素的血浓度)。数据采用方差分析。普拉克索降低了警觉性,导致瞳孔扩张,增加了心率,降低了催乳素和促甲状腺激素水平,并提高了生长激素水平。莫达非尼使血压和核心体温略有升高,并降低了催乳素水平。普拉克索的镇静作用和莫达非尼的自主神经作用与中脑蓝斑通路活动的改变一致;普拉克索后的瞳孔扩张表明动眼神经核的多巴胺能兴奋降低。