A role for cortical nNOS/NK1 neurons in coupling homeostatic sleep drive to EEG slow wave activity

被引:90
作者
Morairty, Stephen R. [1 ]
Dittrich, Lars [1 ]
Pasumarthi, Ravi K. [1 ]
Valladao, Daniel [1 ]
Heiss, Jaime E. [1 ]
Gerashchenko, Dmitry [1 ]
Kilduff, Thomas S. [1 ]
机构
[1] SRI Int, Ctr Neurosci, Biosci Div, Menlo Pk, CA 94025 USA
关键词
sleep homeostasis; cerebral cortex; interneurons; Fos; Nos1; BASAL FOREBRAIN NEURONS; NITRIC-OXIDE PRODUCTION; CEREBRAL-CORTEX; GABAERGIC NEURONS; RECOVERY SLEEP; SUBSTANCE-P; WAKEFULNESS; INTERNEURONS; INHIBITION; INDUCTION;
D O I
10.1073/pnas.1314762110
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Although the neural circuitry underlying homeostatic sleep regulation is little understood, cortical neurons immunoreactive for neuronal nitric oxide synthase (nNOS) and the neurokinin-1 receptor (NK1) have been proposed to be involved in this physiological process. By systematically manipulating the durations of sleep deprivation and subsequent recovery sleep, we show that activation of cortical nNOS/NK1 neurons is directly related to non-rapid eye movement (NREM) sleep time, NREM bout duration, and EEG delta power during NREM sleep, an index of preexisting homeostatic sleep drive. Conversely, nNOS knockout mice show reduced NREM sleep time, shorter NREM bouts, and decreased power in the low delta range during NREM sleep, despite constitutively elevated sleep drive. Cortical NK1 neurons are still activated in response to sleep deprivation in these mice but, in the absence of nNOS, they are unable to up-regulate NREM delta power appropriately. These findings support the hypothesis that cortical nNOS/NK1 neurons translate homeostatic sleep drive into up-regulation of NREM d power through an NO-dependent mechanism.
引用
收藏
页码:20272 / 20277
页数:6
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