Landgraf Dominic, Joiner William J, McCarthy Michael J, Kiessling Silke, Barandas Rita, Young Jared W, Cermakian Nicolas, Welsh David K
VA San Diego Healthcare System, San Diego, CA, USA; Department of Psychiatry, University of California, San Diego, La Jolla, CA, USA; Center for Circadian Biology, University of California, San Diego, La Jolla, CA, USA.
Center for Circadian Biology, University of California, San Diego, La Jolla, CA, USA; Department of Pharmacology, University of California, San Diego, La Jolla, CA, USA.
Neuropharmacology. 2016 Aug;107:262-270. doi: 10.1016/j.neuropharm.2016.03.047. Epub 2016 Mar 28.
Endogenous circadian (∼24 h) clocks regulate key physiological and cognitive processes via rhythmic expression of clock genes. The main circadian pacemaker is the hypothalamic suprachiasmatic nucleus (SCN). Mood disorders, including bipolar disorder (BD), are commonly associated with disturbed circadian rhythms. Dopamine (DA) contributes to mania in BD and has direct impact on clock gene expression. Therefore, we hypothesized that high levels of DA during episodes of mania contribute to disturbed circadian rhythms in BD. The mood stabilizer valproic acid (VPA) also affects circadian rhythms. Thus, we further hypothesized that VPA normalizes circadian disturbances caused by elevated levels of DA. To test these hypotheses, we examined locomotor rhythms and circadian gene cycling in mice with reduced expression of the dopamine transporter (DAT-KD mice), which results in elevated DA levels and mania-like behavior. We found that elevated DA signaling lengthened the circadian period of behavioral rhythms in DAT-KD mice and clock gene expression rhythms in SCN explants. In contrast, we found that VPA shortened circadian period of behavioral rhythms in DAT-KD mice and clock gene expression rhythms in SCN explants, hippocampal cell lines, and human fibroblasts from BD patients. Thus, DA and VPA have opposing effects on circadian period. To test whether the impact of VPA on circadian rhythms contributes to its behavioral effects, we fed VPA to DAT-deficient Drosophila with and without functioning circadian clocks. Consistent with our hypothesis, we found that VPA had potent activity-suppressing effects in hyperactive DAT-deficient flies with intact circadian clocks. However, these effects were attenuated in DAT-deficient flies in which circadian clocks were disrupted, suggesting that VPA functions partly through the circadian clock to suppress activity. Here, we provide in vivo and in vitro evidence across species that elevated DA signaling lengthens the circadian period, an effect remediated by VPA treatment. Hence, VPA may exert beneficial effects on mood by normalizing lengthened circadian rhythm period in subjects with elevated DA resulting from reduced DAT.
内源性昼夜节律(约24小时)时钟通过时钟基因的节律性表达来调节关键的生理和认知过程。主要的昼夜节律起搏器是下丘脑视交叉上核(SCN)。包括双相情感障碍(BD)在内的情绪障碍通常与昼夜节律紊乱有关。多巴胺(DA)在双相情感障碍的躁狂发作中起作用,并对时钟基因表达有直接影响。因此,我们假设躁狂发作期间高水平的多巴胺会导致双相情感障碍患者的昼夜节律紊乱。情绪稳定剂丙戊酸(VPA)也会影响昼夜节律。因此,我们进一步假设丙戊酸可使由多巴胺水平升高引起的昼夜节律紊乱恢复正常。为了验证这些假设,我们研究了多巴胺转运体表达降低的小鼠(DAT-KD小鼠)的运动节律和昼夜节律基因循环,多巴胺转运体表达降低会导致多巴胺水平升高和类似躁狂的行为。我们发现,多巴胺信号增强会延长DAT-KD小鼠行为节律的昼夜周期以及SCN外植体中时钟基因表达的昼夜周期。相反,我们发现丙戊酸缩短了DAT-KD小鼠行为节律的昼夜周期以及SCN外植体、海马细胞系和双相情感障碍患者的人成纤维细胞中时钟基因表达的昼夜周期。因此,多巴胺和丙戊酸对昼夜周期有相反的作用。为了测试丙戊酸对昼夜节律的影响是否有助于其行为效应,我们给有或没有正常昼夜节律时钟的DAT缺陷型果蝇喂食丙戊酸。与我们的假设一致,我们发现丙戊酸对昼夜节律完整的多动DAT缺陷型果蝇有强大的活动抑制作用。然而,在昼夜节律时钟被破坏的DAT缺陷型果蝇中,这些作用减弱了,这表明丙戊酸部分通过昼夜节律时钟发挥作用来抑制活动。在这里,我们提供了跨物种的体内和体外证据,表明多巴胺信号增强会延长昼夜周期,而丙戊酸治疗可纠正这种效应。因此,丙戊酸可能通过使因多巴胺转运体减少导致多巴胺升高的受试者延长的昼夜节律周期恢复正常,从而对情绪产生有益影响。