BK calcium-activated potassium channels regulate circadian behavioral rhythms and pacemaker output

被引:198
作者
Meredith, Andrea L.
Wiler, Steven W.
Miller, Brooke H.
Takahashi, Joseph S.
Fodor, Anthony A.
Ruby, Norman F.
Aldrich, Richard W.
机构
[1] Stanford Univ, Dept Mol & Cellular Physiol, Stanford, CA 94305 USA
[2] Stanford Univ, Howard Hughes Med Inst, Stanford, CA 94305 USA
[3] Northwestern Univ, Dept Neurobiol & Physiol, Evanston, IL 60208 USA
[4] Northwestern Univ, Howard Hughes Med Inst, Evanston, IL 60208 USA
[5] Stanford Univ, Dept Biol Sci, Stanford, CA 94305 USA
关键词
D O I
10.1038/nn1740
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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 Ca2+ 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 Arnt1 (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.
引用
收藏
页码:1041 / 1049
页数:9
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