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中枢组胺能系统参与莫达非尼诱导而非哌甲酯诱导的大鼠运动活动增加。

Involvement of central histaminergic systems in modafinil-induced but not methylphenidate-induced increases in locomotor activity in rats.

作者信息

Ishizuka Tomoko, Murakami Masahiro, Yamatodani Atsushi

机构信息

Department of Medical Science and Technology, Graduate School of Allied Health Sciences, Faculty of Medicine, Osaka University, 565-0871, Osaka, Japan.

出版信息

Eur J Pharmacol. 2008 Jan 14;578(2-3):209-15. doi: 10.1016/j.ejphar.2007.09.009. Epub 2007 Sep 26.

Abstract

Modafinil is a novel wake-promoting drug used for the treatment of narcolepsy, the mechanism of action of which remains unclear. Previous studies have shown that modafinil produces a different pattern of c-Fos activation in the brain to the classical stimulants amphetamine and methylphenidate. Modafinil, given i.p. to urethane-anesthetized rats, is associated with an increase in histamine release from the anterior hypothalamus, indicating that its behavioral actions may involve histaminergic systems. In the present study, the effects of modafinil on histamine release using in vivo microdialysis and locomotor activity in freely moving rats were examined, and compared with those of the classical psychostimulant methylphenidate. Modafinil (75 and 150 mg/kg, i.p.) increased both histamine release and locomotor activity, significantly. Methylphenidate (3 mg/kg, i.p.) also increased locomotor activity to the same extent as modafinil (150 mg/kg, i.p.) without stimulating histamine release. Depletion of neuronal histamine using alpha-fluoromethylhistidine abolished the effect of modafinil on locomotor activity in mice but had no effect on methylphenidate-induced locomotion. Examination of the effects of modafinil and methylphenidate on locomotor activity in the dark phase at doses that produced comparable effects in the light phase showed that the effect of modafinil in the dark phase was less than that of methylphenidate, a possible indication that modafinil-induced locomotor activity may be partly related to its wake-promoting actions. These findings suggest that the locomotor effects of modafinil but not of methylphenidate, involve the central histaminergic systems.

摘要

莫达非尼是一种用于治疗发作性睡病的新型促醒药物,其作用机制尚不清楚。先前的研究表明,莫达非尼在大脑中产生的c-Fos激活模式与经典兴奋剂苯丙胺和哌甲酯不同。给乌拉坦麻醉的大鼠腹腔注射莫达非尼,会导致下丘脑前部组胺释放增加,这表明其行为作用可能涉及组胺能系统。在本研究中,使用体内微透析技术检测了莫达非尼对自由活动大鼠组胺释放和运动活性的影响,并与经典精神兴奋剂哌甲酯进行了比较。莫达非尼(75和150毫克/千克,腹腔注射)显著增加了组胺释放和运动活性。哌甲酯(3毫克/千克,腹腔注射)也使运动活性增加到与莫达非尼(150毫克/千克,腹腔注射)相同的程度,但未刺激组胺释放。使用α-氟甲基组氨酸耗尽神经元组胺消除了莫达非尼对小鼠运动活性的影响,但对哌甲酯诱导的运动没有影响。在黑暗阶段检测莫达非尼和哌甲酯在产生与光照阶段相当效果的剂量下对运动活性的影响,结果表明莫达非尼在黑暗阶段的作用小于哌甲酯,这可能表明莫达非尼诱导的运动活性可能部分与其促醒作用有关。这些发现表明,莫达非尼而非哌甲酯的运动作用涉及中枢组胺能系统。

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