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首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >Identification and characterization of a sleep-active cell group in the rostral medullary brainstem
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Identification and characterization of a sleep-active cell group in the rostral medullary brainstem

机译:延髓延髓脑干中睡眠活动细胞群的鉴定和表征

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Early transection and stimulation studies suggested the existence of sleep-promoting circuitry in the medullary brainstem, yet the location and identity of the neurons comprising this putative hypnogenic circuitry remains unresolved. In the present study, we sought to uncover the location and identity of medullary neurons that might contribute to the regulation of sleep. Here we show the following in rats: (1) a delimited node of medullary neurons located lateral and dorsal to the facial nerve-a region we termed the parafacial zone (PZ)-project to the wake-promoting medial parabrachial nucleus; (2)PZneurons express c-Fos after sleep but not after wakefulness and hence are sleep active; and (3) cell-body-specific lesions of the PZ result in large and sustained increases (50%) in daily wakefulness at the expense of slow-wave sleep (SWS). Using transgenic reporter mice [vesicular GABA/glycine transporter (Vgat)-GFP], we then show that 50% of PZ sleep-active neurons are inhibitory (GABAergic/glycinergic, VGAT-positive) in nature. Finally, we used a Cre-expressing adeno-associated viral vector and conditional Vgatlox/lox mice to selectively and genetically disrupt GABA/glycinergic neurotransmission from PZ neurons. Disruption of PZ GABAergic/glycinergic neurotransmission resulted in sustained increases (40%) in daily wakefulness at the expense of both SWS and rapid eye movement sleep. These results together reveal the location and neurochemical identity of a delimited node of sleep-active neurons within the rostral medullary brainstem.
机译:早期横断和刺激研究表明,延髓脑干中存在促进睡眠的电路,但是构成这种推定的催眠电路的神经元的位置和特性仍未得到解决。在本研究中,我们试图揭示可能有助于调节睡眠的髓质神经元的位置和特性。在这里,我们在大鼠中显示以下内容:(1)位于面神经外侧和背侧的延髓神经元定界结点-我们称其为面旁区(PZ)-投射至促尾肌内侧臂旁核的区域; (2)PZneurons在睡眠后表达c-Fos,但在清醒后不表达,因此活跃睡眠。 (3)PZ的细胞体特异性病变会导致每日清醒性的大量持续增长(50%),但以慢波睡眠(SWS)为代价。然后,使用转基因报告基因小鼠[囊泡GABA /甘氨酸转运蛋白(Vgat)-GFP],我们发现> 50%的PZ睡眠活性神经元在自然界具有抑制作用(GABA能/甘氨酸能,VGAT阳性)。最后,我们使用表达Cre的腺相关病毒载体和条件性Vgatlox / lox小鼠选择性地和遗传性地破坏了PZ神经元的GABA /甘氨酸能神经传递。 PZ GABA能/甘氨酸能神经传递的中断导致每日清醒持续增加(40%),这是以SWS和快速眼动睡眠为代价的。这些结果共同揭示了延髓延髓脑干内睡眠活动神经元定界节点的位置和神经化学特性。

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