Department of Neurology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA, USA.
Eur J Neurosci. 2010 Feb;31(3):499-507. doi: 10.1111/j.1460-9568.2009.07062.x. Epub 2010 Jan 25.
The basal ganglia (BG) are involved in numerous neurobiological processes that operate on the basis of wakefulness, including motor function, learning, emotion and addictive behaviors. We hypothesized that the BG might play an important role in the regulation of wakefulness. To test this prediction, we made cell body-specific lesions in the striatum and globus pallidus (GP) using ibotenic acid. We found that rats with striatal (caudoputamen) lesions exhibited a 14.95% reduction in wakefulness and robust fragmentation of sleep-wake behavior, i.e. an increased number of state transitions and loss of ultra-long wake bouts (> 120 min). These lesions also resulted in a reduction in the diurnal variation of sleep-wakefulness. On the other hand, lesions of the accumbens core resulted in a 26.72% increase in wakefulness and a reduction in non-rapid eye movement (NREM) sleep bout duration. In addition, rats with accumbens core lesions exhibited excessive digging and scratching. GP lesions also produced a robust increase in wakefulness (45.52%), and frequent sleep-wake transitions and a concomitant decrease in NREM sleep bout duration. Lesions of the subthalamic nucleus or the substantia nigra reticular nucleus produced only minor changes in the amount of sleep-wakefulness and did not alter sleep architecture. Finally, power spectral analysis revealed that lesions of the striatum, accumbens and GP slowed down the cortical electroencephalogram. Collectively, our results suggest that the BG, via a cortico-striato-pallidal loop, are important neural circuitry regulating sleep-wake behaviors and cortical activation.
基底神经节(BG)参与了许多基于觉醒的神经生物学过程,包括运动功能、学习、情绪和成瘾行为。我们假设 BG 可能在觉醒的调节中发挥重要作用。为了验证这一预测,我们使用异硫氰酸对纹状体和苍白球(GP)进行了细胞体特异性损伤。我们发现,纹状体(尾壳核)损伤的大鼠表现出觉醒减少 14.95%,睡眠-觉醒行为严重碎片化,即状态转换次数增加和超长觉醒期丧失(>120 分钟)。这些损伤还导致睡眠-觉醒的昼夜变化减少。另一方面,伏隔核核心的损伤导致觉醒增加 26.72%,非快速眼动(NREM)睡眠期持续时间减少。此外,伏隔核核心损伤的大鼠表现出过度挖掘和抓挠。GP 损伤也导致觉醒显著增加(45.52%),频繁的睡眠-觉醒转换以及 NREM 睡眠期持续时间相应减少。丘脑底核或黑质网状核的损伤仅导致睡眠-觉醒量的微小变化,并且不改变睡眠结构。最后,功率谱分析表明,纹状体、伏隔核和 GP 的损伤使皮层脑电图减慢。总的来说,我们的结果表明,BG 通过皮质-纹状体-苍白球环路,是调节睡眠-觉醒行为和皮层激活的重要神经回路。