State Key Laboratory of Medical Neurobiology, Shanghai Medical College of Fudan University, Shanghai, China.
PLoS One. 2012;7(9):e45471. doi: 10.1371/journal.pone.0045471. Epub 2012 Sep 19.
We have previously shown that modafinil promotes wakefulness via dopamine receptor D(1) and D(2) receptors; however, the locus where dopamine acts has not been identified. We proposed that the nucleus accumbens (NAc) that receives the ventral tegmental area dopamine inputs play an important role not only in reward and addiction but also in sleep-wake cycle and in mediating modafinil-induced arousal.
METHODOLOGY/PRINCIPAL FINDINGS: In the present study, we further explored the role of NAc in sleep-wake cycle and sleep homeostasis by ablating the NAc core and shell, respectively, and examined arousal response following modafinil administration. We found that discrete NAc core and shell lesions produced 26.5% and 17.4% increase in total wakefulness per day, respectively, with sleep fragmentation and a reduced sleep rebound after a 6-hr sleep deprivation compared to control. Finally, NAc core but not shell lesions eliminated arousal effects of modafinil.
CONCLUSIONS/SIGNIFICANCE: These results indicate that the NAc regulates sleep-wake behavior and mediates arousal effects of the midbrain dopamine system and stimulant modafinil.
我们之前的研究表明,莫达非尼通过多巴胺受体 D1 和 D2 促进觉醒;然而,多巴胺作用的位置尚未确定。我们提出,伏隔核(NAc)接收腹侧被盖区多巴胺输入,不仅在奖励和成瘾中发挥重要作用,而且在睡眠-觉醒周期中以及调节莫达非尼诱导的觉醒中发挥重要作用。
方法/主要发现:在本研究中,我们通过分别破坏 NAc 核心和壳,进一步探讨了 NAc 在睡眠-觉醒周期和睡眠稳态中的作用,并检查了莫达非尼给药后的觉醒反应。我们发现,离散的 NAc 核心和壳损伤分别导致每天总觉醒时间增加 26.5%和 17.4%,与对照组相比,睡眠碎片化和 6 小时睡眠剥夺后的睡眠反弹减少。最后,NAc 核心而不是壳损伤消除了莫达非尼的觉醒作用。
结论/意义:这些结果表明,NAc 调节睡眠-觉醒行为,并介导中脑多巴胺系统和兴奋剂莫达非尼的觉醒作用。