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Striatal adenosine A2A receptor neurons control active-period sleep via parvalbumin neurons in external globus pallidus

机译:纹状体腺苷A2A受体神经元通过苍白球外小白蛋白神经元控制活动期睡眠

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摘要

Dysfunction of the striatum is frequently associated with sleep disturbances. However, its role in sleep-wake regulation has been paid little attention even though the striatum densely expresses adenosine A2A receptors (A2ARs), which are essential for adenosine-induced sleep. Here we showed that chemogenetic activation of A2AR neurons in specific subregions of the striatum induced a remarkable increase in non-rapid eye movement (NREM) sleep. Anatomical mapping and immunoelectron microscopy revealed that striatal A2AR neurons innervated the external globus pallidus (GPe) in a topographically organized manner and preferentially formed inhibitory synapses with GPe parvalbumin (PV) neurons. Moreover, lesions of GPe PV neurons abolished the sleep-promoting effect of striatal A2AR neurons. In addition, chemogenetic inhibition of striatal A2AR neurons led to a significant decrease of NREM sleep at active period, but not inactive period of mice. These findings reveal a prominent contribution of striatal A2AR neuron/GPe PV neuron circuit in sleep control.
机译:纹状体功能障碍通常与睡眠障碍有关。但是,即使纹状体密集表达腺苷诱导的睡眠所必需的腺苷A2A受体(A2ARs),其在睡眠觉醒调节中的作用也很少受到关注。在这里,我们显示了纹状体特定子区域中A2AR神经元的化学生成激活,导致非快速眼动(NREM)睡眠显着增加。解剖图和免疫电子显微镜显示,纹状体A2AR神经元以地形组织方式支配了外部苍白球(GPe),并优先与GPe小白蛋白(PV)神经元形成抑制性突触。此外,GPe PV神经元的损伤消除了纹状体A2AR神经元的促睡眠作用。此外,纹状体A2AR神经元的化学发生抑制作用导致小鼠活动期而非活动期的NREM睡眠显着减少。这些发现揭示了纹状体A2AR神经元/ GPe PV神经元回路在睡眠控制中的显着贡献。

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