Department of Psychology, Center for Studies in Behavioral Neurobiology/FRSQ Groupe de Recherche en Neurobiologie Comportementale, Concordia University, 7141 Sherbrooke Street West, SP-244, Montreal, QC, H4B 1R6, Canada.
J Mol Neurosci. 2011 Oct;45(2):154-61. doi: 10.1007/s12031-010-9469-z. Epub 2010 Nov 10.
The circadian clock in the mammalian suprachiasmatic nucleus (SCN) can be entrained by light cycles longer than the normal 24-h light/dark (LD) cycle, but little is known about the effect of such cycles on circadian clocks outside the SCN. Here we examined the effect of exposure to a 26-h T cycle (T26, 1 h:25 h LD) on patterns of expression of the clock protein, PERIOD2 (PER2), in the SCN and in four regions of the limbic forebrain known to exhibit robust circadian oscillations in PER2: the oval nucleus of the bed nucleus of the stria terminalis (BNSTov), central nucleus of the amygdala (CEA), basolateral amygdala (BLA), and dentate gyrus (DG). All rats showed stable entrainment of running wheel activity rhythms to the T26 cycle. As previously shown, PER2 expression in the SCN was stably entrained, peaking around the onset of locomotor activity. In contrast, exposure to the T26 cycle uncoupled the rhythms of PER2 expression in the BNSTov and CEA from that of the SCN, whereas PER2 rhythms in the BLA and DG were unaffected. These results show that exposure to long light cycles can uncouple circadian oscillators in select nuclei of the limbic forebrain from the SCN clock and suggest that such cycles may be used to study the functional consequences of coupling and uncoupling of brain circadian oscillators.
哺乳动物视交叉上核(SCN)中的生物钟可以被长于正常 24 小时光/暗(LD)周期的光周期重新同步,但对于 SCN 以外的生物钟受此类周期影响的情况知之甚少。在这里,我们研究了暴露于 26 小时 T 周期(T26,1 h:25 h LD)对 SCN 中时钟蛋白 PERIOD2(PER2)表达模式以及四个已知在 PER2 中表现出强烈昼夜节律的边缘前脑区域表达模式的影响:终纹床核的卵圆形核(BNSTov)、杏仁核中央核(CEA)、杏仁核基底外侧核(BLA)和齿状回(DG)。所有大鼠的跑步轮活动节律均稳定地与 T26 周期同步。如前所述,SCN 中的 PER2 表达稳定地与活动开始同步。相比之下,暴露于 T26 周期会使 BNSTov 和 CEA 中的 PER2 表达节律与 SCN 的节律脱钩,而 BLA 和 DG 中的 PER2 节律不受影响。这些结果表明,暴露于长光周期会使边缘前脑的特定核中的生物钟与 SCN 时钟脱钩,并表明此类周期可用于研究大脑生物钟的耦合和脱耦的功能后果。