Center for Neuroscience, Biosciences Division, SRI International, Menlo Park, CA, USA.
Institute for Neurogenomics, Helmholtz Zentrum München, German Research Centre for Environmental Health, Neuherberg, Germany.
Cereb Cortex. 2019 Mar 1;29(3):1090-1108. doi: 10.1093/cercor/bhy015.
We have proposed that cortical nNOS/NK1R interneurons have a role in sleep homeostasis. The hypocretins (orexins) are wake-promoting neuropeptides and hypocretin/orexin (Hcrt) neurons project to the cortex. Hcrt peptides affect deep layer cortical neurons, and Hcrt receptor 1 (Hcrtr1; Ox1r) mRNA is expressed in cortical nNOS/NK1R cells. Therefore, we investigated whether Hcrt neuron stimulation affects cingulate cortex nNOS/NK1R neurons. Bath application of HCRT1/orexin-A evoked an inward current and membrane depolarization in most nNOS/NK1R cells which persisted in tetrodotoxin; optogenetic stimulation of Hcrt terminals expressing channelrhodopsin-2 confirmed these results, and pharmacological studies determined that HCRTR1 mediated these responses. Single-cell RT-PCR found Hcrtr1 mRNA in 31% of nNOS/NK1R cells without any Hcrtr2 mRNA expression; immunohistochemical studies of Hcrtr1-EGFP mice confirmed that a minority of nNOS/NK1R cells express HCRTR1. When Hcrt neurons degenerated in orexin-tTA;TetO DTA mice, the increased EEG delta power during NREM sleep produced in response to 4 h sleep deprivation and c-FOS expression in cortical nNOS/NK1R cells during recovery sleep were indistinguishable from that of controls. We conclude that Hcrt excitatory input to these deep layer cells is mediated through HCRTR1 but is unlikely to be involved in the putative role of cortical nNOS/NK1R neurons in sleep homeostasis.
我们提出,皮质 nNOS/NK1R 中间神经元在睡眠稳态中起作用。食欲肽(orexins)是促进觉醒的神经肽,食欲肽/orexin(Hcrt)神经元投射到皮质。Hcrt 肽影响皮质深层神经元,皮质 nNOS/NK1R 细胞表达 Hcrt 受体 1(Hcrtr1;Ox1r)mRNA。因此,我们研究了 Hcrt 神经元刺激是否影响扣带回皮质 nNOS/NK1R 神经元。HCRT1/orexin-A 的浴应用在大多数 nNOS/NK1R 细胞中诱发内向电流和膜去极化,该电流在河豚毒素中持续存在;光遗传学刺激表达通道视紫红质-2 的 Hcrt 末梢证实了这些结果,药物研究确定 HCRTR1 介导了这些反应。单细胞 RT-PCR 在没有任何 Hcrtr2 mRNA 表达的情况下发现 31%的 nNOS/NK1R 细胞中存在 Hcrtr1 mRNA;Hcrtr1-EGFP 小鼠的免疫组织化学研究证实,少数 nNOS/NK1R 细胞表达 HCRTR1。当 orexin-tTA;TetO DTA 小鼠中的 Hcrt 神经元退化时,4 小时睡眠剥夺后 NREM 睡眠期间 EEG 三角波功率的增加以及恢复睡眠期间皮质 nNOS/NK1R 细胞中的 c-FOS 表达与对照组无明显区别。我们得出结论,这些深层细胞的 Hcrt 兴奋性输入是通过 HCRTR1 介导的,但不太可能参与皮质 nNOS/NK1R 神经元在睡眠稳态中的潜在作用。