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儿茶酚胺耗竭诱导的困倦的神经相关物。

Neural correlates of sleepiness induced by catecholamine depletion.

机构信息

National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Psychiatry Res. 2011 Oct 31;194(1):73-8. doi: 10.1016/j.pscychresns.2011.06.015. Epub 2011 Aug 27.

Abstract

Although extensive indirect evidence exists to suggest that the central dopaminergic system plays a significant role in the modulation of arousal, the functional effect of the dopaminergic influence on the regulation of the sleep-wake cycle remains unclear. Thirteen healthy volunteers and 15 unmedicated subjects with a history of major depressive disorder underwent catecholamine depletion (CD) using oral alpha-methyl-para-tyrosine in a randomized, placebo-controlled, double-blind, crossover study. The main outcome measures in both sessions were sleepiness (Stanford-Sleepiness-Scale), cerebral glucose metabolism (positron emission tomography), and serum prolactin concentration. CD consistently induced clinically relevant sleepiness in both groups. The CD-induced prolactin increase significantly correlated with CD-induced sleepiness but not with CD-induced mood and anxiety symptoms. CD-induced sleepiness correlated with CD-induced increases in metabolism in the medial and orbital frontal cortex, bilateral superior temporal cortex, left insula, cingulate motor area and in the vicinity of the periaqueductal gray. This study suggests that the association between dopamine depletion and sleepiness is independent of the brain reward system and the risk for depression. The visceromotor system, the cingulate motor area, the periaqueductal gray and the caudal hypothalamus may mediate the impact of the dopaminergic system on regulation of wakefulness and sleep.

摘要

虽然有大量间接证据表明,中枢多巴胺系统在调节觉醒方面起着重要作用,但多巴胺对睡眠-觉醒周期的调节的功能影响仍不清楚。13 名健康志愿者和 15 名未经药物治疗的有重度抑郁症病史的患者参加了一项随机、安慰剂对照、双盲、交叉研究,通过口服α-甲基-对酪氨酸进行儿茶酚胺耗竭 (CD)。在两个疗程中,主要的评估指标是困倦(斯坦福嗜睡量表)、大脑葡萄糖代谢(正电子发射断层扫描)和血清催乳素浓度。CD 在两组中均持续诱导出具有临床相关性的困倦。CD 诱导的催乳素增加与 CD 诱导的困倦显著相关,但与 CD 诱导的情绪和焦虑症状无关。CD 诱导的困倦与 CD 诱导的中侧额皮质、双侧颞上皮质、左侧岛叶、扣带回运动区和导水管周围灰质附近的代谢增加相关。这项研究表明,多巴胺耗竭与困倦之间的关联独立于大脑奖励系统和抑郁风险。内脏运动系统、扣带回运动区、导水管周围灰质和下丘脑尾部可能介导多巴胺系统对觉醒和睡眠调节的影响。

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Neural correlates of sleepiness induced by catecholamine depletion.儿茶酚胺耗竭诱导的困倦的神经相关物。
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