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Sleep deprivation differentially affects dopamine receptor subtypes in mouse striatum.

机译:睡眠剥夺差异地影响小鼠纹状体中的多巴胺受体亚型。

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The effects of sleep deprivation on dopaminergic systems remain elusive, in part due to the lack of selective ligands for dopamine receptor subtypes. We examined D1, D2, and D3 receptor density in the mouse brain after sleep deprivation by receptor autoradiography using [H]SCH 23390 for D1R, [H]raclopride for D2R, and [H]WC-10 for D3R (a novel D3R-selective compound developed in our laboratory, not previously reported in mouse). Sleep-deprived mice showed a significant decrease in D1R, no change in D2R, and a significant increase in D3R binding in striatum. This pattern of dopamine receptor changes was not seen in mice subjected to restraint stress, suggesting specificity to sleep. These data provide evidence that brain dopaminergic circuits are remodeled after sleep deprivation.
机译:缺乏睡眠对多巴胺能系统的影响仍然难以捉摸,部分原因是缺乏对多巴胺受体亚型的选择性配体。我们通过[X] SCH 23390的D1R,[H] raclopride的D2R和[H] WC-10的D3R(一种新型的D3R-在我们实验室开发的选择性化合物,以前未在小鼠中报道过)。睡眠不足的小鼠显示纹状体中D1R显着降低,D2R无变化,D3R结合显着增加。在受到束缚压力的小鼠中未观察到这种多巴胺受体改变的模式,表明对睡眠具有特异性。这些数据提供了睡眠剥夺后大脑多巴胺能回路被重塑的证据。

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