Kodama Tohru, Kojima Takashi, Honda Yoshiko, Hosokawa Takayuki, Tsutsui Ken-Ichiro, Watanabe Masataka
Department of Physiological Psychology, Tokyo Metropolitan Institute of Medical Science, Setagaya, Tokyo 156-8506, Japan, and.
Division of Systems Neuroscience, Tohoku University Graduate School of Life Sciences, Aoba-ku, Sendai 980-8577, Japan.
J Neurosci. 2017 Mar 1;37(9):2387-2394. doi: 10.1523/JNEUROSCI.2155-16.2017. Epub 2017 Feb 2.
Methylphenidate (MPH; trade name Ritalin) is a widely used drug for the treatment of attention deficit hyperactivity disorder (ADHD) and is often used as a cognitive enhancer. Because MPH increases dopamine (DA) release by blocking the DA transporter in the human striatum, MPH is supposed to work on attention and cognition through a DA increase in the striatum. However, ADHD patients show impaired prefrontal cortex (PFC) function and MPH administration is associated with increased neural activity in the PFC. Although MPH is indicated to increase DA release in the rat PFC, there has been no study to examine MPH-induced DA changes in the human PFC because of technical difficulties associated with the low level of PFC DA receptors. Using the microdialysis technique, we examined the effects of oral administration of MPH on DA release in both the PFC and striatum in the monkey. We also tested the effect of MPH on cognitive task performance. As in human studies, in the striatum, both high and low doses of MPH induced consistent increases in DA release ∼30 min after their administrations. In the PFC, a consistent increase in DA release was observed 1 h after a high dose, but not low doses, of MPH. Low doses of MPH improved cognitive task performance, but a high dose of MPH made the monkey drowsy. Therefore, low-dose MPH-induced cognitive enhancement is supported by striatum DA increase. Methylphenidate (MPH) is a widely used drug for the treatment of attention deficit hyperactivity disorder and is often used as a cognitive enhancer. Although human positron emission tomography studies suggest that MPH works on attention and cognition through dopamine (DA) changes in the striatum, there has been no study to examine MPH-induced DA changes in the human prefrontal cortex (PFC). Using the microdialysis technique in monkeys, we found, for the first time, that low doses of MPH consistently increased DA release in the striatum but did not in the PFC. Cognitive enhancement effects of low doses of MPH are supposed to be supported by the striatum DA increase.
哌甲酯(MPH;商品名利他林)是一种广泛用于治疗注意力缺陷多动障碍(ADHD)的药物,常被用作认知增强剂。由于MPH通过阻断人类纹状体中的多巴胺(DA)转运体来增加DA释放,因此MPH被认为是通过增加纹状体中的DA来作用于注意力和认知。然而,ADHD患者表现出前额叶皮质(PFC)功能受损,且服用MPH与PFC神经活动增加有关。尽管有研究表明MPH可增加大鼠PFC中的DA释放,但由于PFC中DA受体水平较低带来的技术困难,尚无研究检测MPH诱导的人类PFC中DA的变化。我们使用微透析技术,研究了口服MPH对猴子PFC和纹状体中DA释放的影响。我们还测试了MPH对认知任务表现的影响。与人体研究一样,在纹状体中,高剂量和低剂量的MPH给药后约30分钟均能持续增加DA释放。在PFC中,高剂量而非低剂量的MPH给药1小时后可观察到DA释放持续增加。低剂量的MPH改善了认知任务表现,但高剂量的MPH使猴子昏昏欲睡。因此,低剂量MPH诱导的认知增强得到纹状体DA增加的支持。哌甲酯(MPH)是一种广泛用于治疗注意力缺陷多动障碍的药物,常被用作认知增强剂。尽管人类正电子发射断层扫描研究表明MPH通过纹状体中多巴胺(DA)的变化作用于注意力和认知,但尚无研究检测MPH诱导的人类前额叶皮质(PFC)中DA的变化。通过在猴子身上使用微透析技术,我们首次发现低剂量的MPH能持续增加纹状体中的DA释放,但在PFC中却不能。低剂量MPH的认知增强作用被认为是由纹状体DA增加所支持的。