Meredith Andrea L, Wiler Steven W, Miller Brooke H, Takahashi Joseph S, Fodor Anthony A, Ruby Norman F, Aldrich Richard W
Department of Molecular and Cellular Physiology and Howard Hughes Medical Institute, Stanford University, Stanford, California 94305, USA.
Nat Neurosci. 2006 Aug;9(8):1041-9. doi: 10.1038/nn1740. Epub 2006 Jul 16.
Spontaneous action potentials in the suprachiasmatic nucleus (SCN) are necessary for normal circadian timing of behavior in mammals. The SCN exhibits a daily oscillation in spontaneous firing rate (SFR), but the ionic conductances controlling SFR and the relationship of SFR to subsequent circadian behavioral rhythms are not understood. We show that daily expression of the large conductance Ca(2+)-activated K(+) channel (BK) in the SCN is controlled by the intrinsic circadian clock. BK channel-null mice (Kcnma1(-/-)) have increased SFRs in SCN neurons selectively at night and weak circadian amplitudes in multiple behaviors timed by the SCN. Kcnma1(-/-) mice show normal expression of clock genes such as Arntl (Bmal1), indicating a role for BK channels in SCN pacemaker output, rather than in intrinsic time-keeping. Our findings implicate BK channels as important regulators of the SFR and suggest that the SCN pacemaker governs the expression of circadian behavioral rhythms through SFR modulation.
视交叉上核(SCN)中的自发动作电位对于哺乳动物行为的正常昼夜节律至关重要。SCN的自发放电率(SFR)呈现每日振荡,但控制SFR的离子电导以及SFR与随后昼夜行为节律的关系尚不清楚。我们发现SCN中大通量钙激活钾通道(BK)的每日表达受内在生物钟控制。BK通道缺失小鼠(Kcnma1(-/-))在夜间SCN神经元中的SFR选择性增加,并且在由SCN定时的多种行为中昼夜节律幅度减弱。Kcnma1(-/-)小鼠显示时钟基因如Arntl(Bmal1)的正常表达,表明BK通道在SCN起搏器输出中起作用,而非在内在计时中起作用。我们的研究结果表明BK通道是SFR的重要调节因子,并提示SCN起搏器通过SFR调节来控制昼夜行为节律的表达。