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锂影响脉络丛中的生物钟——旧机制的新作用。

Lithium affects the circadian clock in the choroid plexus - A new role for an old mechanism.

机构信息

Laboratory of Biological Rhythms, Institute of Physiology of the Czech Academy of Sciences, Prague, Czech Republic.

Laboratory of Biological Rhythms, Institute of Physiology of the Czech Academy of Sciences, Prague, Czech Republic.

出版信息

Biomed Pharmacother. 2023 Mar;159:114292. doi: 10.1016/j.biopha.2023.114292. Epub 2023 Jan 24.

DOI:10.1016/j.biopha.2023.114292
PMID:36701987
Abstract

Lithium is an effective mood stabilizer, but the mechanism of its therapeutic action is not well understood. We investigated the effect of lithium on the circadian clock located in the ventricle barrier complex containing the choroid plexus (CP), a part of the glymphatic system that influences gross brain function via the production of cerebrospinal fluid. The mPer2 mice were injected with lithium chloride (LiCl) or vehicle, and their effects on the clock gene Nr1d1 in CP were detected by RT qPCR. CP organotypic explants were prepared to monitor bioluminescence rhythms in real time and examine the responses of the CP clock to LiCl and inhibitors of glycogen synthase kinase-3 (CHIR-99021) and protein kinase C (chelerythrine). LiCl affected Nr1d1 expression levels in CP in vivo and dose-dependently delayed the phase and prolonged the period of the CP clock in vitro. LiCl and CHIR-99021 had different effects on 1] CP clock parameters (amplitude, period, phase), 2] dexamethasone-induced phase shifts of the CP clock, and 3] dynamics of PER2 degradation and de novo accumulation. LiCl-induced phase delays were significantly reduced by chelerythrine, suggesting the involvement of PKC activity. The effects on the CP clock may be involved in the therapeutic effects of lithium and hypothetically improve brain function in psychiatric patients by aligning the function of the CP clock-related glymphatic system with the sleep-wake cycle. Importantly, our data argue for personalized timing of lithium treatment in BD patients.

摘要

锂是一种有效的情绪稳定剂,但它的治疗作用机制尚未得到很好的理解。我们研究了锂对位于含有脉络丛(CP)的脑室壁复合体中的生物钟的影响,CP 是神经胶淋巴系统的一部分,通过产生脑脊液来影响大脑的整体功能。用氯化锂(LiCl)或载体处理 mPer2 小鼠,并通过 RT-qPCR 检测 CP 中时钟基因 Nr1d1 的变化。制备 CP 器官型外植体以实时监测生物发光节律,并研究 CP 时钟对 LiCl 和糖原合酶激酶-3(CHIR-99021)和蛋白激酶 C(白屈菜红碱)抑制剂的反应。LiCl 影响体内 CP 中的 Nr1d1 表达水平,并呈剂量依赖性地延迟 CP 时钟的相位并延长其周期。LiCl 和 CHIR-99021 对 CP 时钟参数(振幅、周期、相位)、CP 时钟的地塞米松诱导的相移以及 PER2 降解和从头积累的动力学有不同的影响。白屈菜红碱显著降低了 LiCl 诱导的相移,表明 PKC 活性的参与。对 CP 时钟的影响可能与锂的治疗作用有关,并通过使 CP 时钟相关神经胶淋巴系统的功能与睡眠-觉醒周期相吻合,从而改善精神病患者的大脑功能。重要的是,我们的数据为双相情感障碍患者的锂治疗时间的个性化提供了依据。

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