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      Direct activation of cardiac pacemaker channels by intracellular cyclic AMP.

      Nature

      Biological Clocks, physiology, Cyclic AMP, metabolism, Cyclic CMP, Cyclic GMP, Electrophysiology, GTP-Binding Proteins, In Vitro Techniques, Ion Channels, Myocardium, Phosphorylation, Sinoatrial Node

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          Abstract

          Cyclic AMP acts as a second messenger in the modulation of several ion channels that are typically controlled by a phosphorylation process. In cardiac pacemaker cells, adrenaline and acetylcholine regulate the hyperpolarization-activated current (if), but in opposite ways; this current is involved in the generation and modulation of pacemaker activity. These actions are mediated by cAMP and underlie control of spontaneous rate by neurotransmitters. Whether the cAMP modulation of if is mediated by channel phosphorylation is, however, still unknown. Here we investigate the action of cAMP on if in excised patches of cardiac pacemaker cells and find that cAMP activates if by a mechanism independent of phosphorylation, involving a direct interaction with the channels at their cytoplasmic side. Cyclic AMP activates if by shifting its activation curve to more positive voltages, in agreement with whole-cell results. This is the first evidence of an ion channel whose gating is dually regulated by voltage and direct cAMP binding.

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          Journal
          1709448
          10.1038/351145a0

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