Ishizuka Tomoko, Sakamoto Yasuhiko, Sakurai Toshimi, Yamatodani Atsushi
Department of Medical Physics, School of Allied Health Sciences, Faculty of Medicine, Osaka University, 1-7 Yamadaoka, Suita, Osaka 565-0871, Japan.
Neurosci Lett. 2003 Mar 20;339(2):143-6. doi: 10.1016/s0304-3940(03)00006-5.
Modafinil, (RS)-2-(Diphenylmethylsulfinyl)acetamide, is a well known wake promoting drug used for the treatment of narcolepsy. We investigated the effect of modafinil on the hypothalamic histamine release in the anesthetized rat using in vivo microdialysis. Modafinil (150 mg/kg, i.p.) increased histamine release by 150% of the basal release. The intracerebroventricular (i.c.v.) injection of modafinil (1 nmol) also increased histamine release, however, when modafinil (1 nmol) was injected directly into the tuberomammillary nucleus, a limited region where cell bodies of the histaminergic neurons are located, histamine release was not altered. These observations suggest that modafinil may promote waking via the activation of the histaminergic system, although it does not appear to be a direct pharmacological target of modafinil.
莫达非尼,(RS)-2-(二苯基甲基亚磺酰基)乙酰胺,是一种用于治疗发作性睡病的知名促醒药物。我们使用体内微透析技术研究了莫达非尼对麻醉大鼠下丘脑组胺释放的影响。莫达非尼(150毫克/千克,腹腔注射)使组胺释放量增加至基础释放量的150%。脑室内注射莫达非尼(1纳摩尔)也会增加组胺释放,然而,当将莫达非尼(1纳摩尔)直接注射到结节乳头体核(组胺能神经元胞体所在的有限区域)时,组胺释放并未改变。这些观察结果表明,莫达非尼可能通过激活组胺能系统来促进觉醒,尽管它似乎不是莫达非尼的直接药理学靶点。