Division of Brain Sciences, Institute for Advanced Medical Research, Keio University School of Medicine, Shinjuku-ku, Tokyo 160-8582, Japan
Faculty of Science and Technology, Keio University, Kohoku-ku, Yokohama, Kanagawa 223-8522, Japan.
eNeuro. 2023 Sep 28;10(9). doi: 10.1523/ENEURO.0327-23.2023. Print 2023 Sep.
Dopamine receptor type 2-expressing medium spiny neurons (D2-MSNs) in the medial part of the ventral striatum (VS) induce non-REM (NREM) sleep from the wake state in animals. However, it is unclear whether D2-MSNs in the lateral part of the VS (VLS), which is anatomically and functionally different from the medial part of the VS, contribute to sleep-wake regulation. This study aims to clarify whether and how D2-MSNs in the VLS are involved in sleep-wake regulation. Our study found that specifically removing D2-MSNs in the VLS led to an increase in wakefulness time in mice during the dark phase using a diphtheria toxin-mediated cell ablation/dysfunction technique. D2-MSN ablation throughout the VS further increased dark phase wakefulness time. These findings suggest that VLS D2-MSNs may induce sleep during the dark phase with the medial part of the VS. Next, our fiber photometric recordings revealed that the population intracellular calcium (Ca) signal in the VLS D2-MSNs increased during the transition from wake to NREM sleep. The mean Ca signal level of VLS D2-MSNs was higher during NREM and REM sleep than during the wake state, supporting their sleep-inducing role. Finally, optogenetic activation of the VLS D2-MSNs during the wake state always induced NREM sleep, demonstrating the causality of VLS D2-MSNs activity with sleep induction. Additionally, activation of the VLS D1-MSNs, counterparts of D2-MSNs, always induced wake from NREM sleep, indicating a wake-promoting role. In conclusion, VLS D2-MSNs could have an NREM sleep-inducing function in coordination with those in the medial VS.
腹侧纹状体(VS)内侧部表达多巴胺受体 2 的中型棘状神经元(D2-MSNs)可在动物从清醒状态诱导非快速眼动(NREM)睡眠。然而,尚不清楚在 VS 外侧部(VLS)的 D2-MSNs 是否有助于睡眠-觉醒调节,因为 VLS 在解剖学和功能上与 VS 内侧部不同。本研究旨在阐明 VLS 的 D2-MSNs 是否以及如何参与睡眠-觉醒调节。我们的研究发现,使用白喉毒素介导的细胞消融/功能障碍技术,特异性去除 VLS 中的 D2-MSNs 会导致小鼠在暗期清醒时间增加。整个 VS 中的 D2-MSN 消融进一步增加了暗期觉醒时间。这些发现表明,VLS 的 D2-MSNs 可能与 VS 的内侧部一起在暗期诱导睡眠。接下来,我们的光纤光度记录显示,VLS 的 D2-MSNs 中的群体细胞内钙(Ca)信号在从觉醒到 NREM 睡眠的转变过程中增加。VLS 的 D2-MSNs 的平均 Ca 信号水平在 NREM 和 REM 睡眠期间高于觉醒状态,支持其诱导睡眠的作用。最后,在觉醒状态下光遗传学激活 VLS 的 D2-MSNs 总是诱导 NREM 睡眠,证明了 VLS 的 D2-MSNs 活性与诱导睡眠之间的因果关系。此外,VLS 的 D1-MSNs(D2-MSNs 的对应物)的激活总是会将 NREM 睡眠唤醒,表明其具有促进觉醒的作用。总之,VLS 的 D2-MSNs 可能与 VS 内侧部的 D2-MSNs 协调发挥诱导 NREM 睡眠的作用。