Ed by the 1st pulse of reapplied voltage steps after administration of acacetin. This property is different from that in blocking open 125-65-5 biological activity channels of hKv1.5 [17]. The blockade of hKv4.3 and hKv1.5 channels by acacetin is likely from cytoplasmic surface, because both hKv4.3 current and hKv1.5 current were not significantly inhibited by intracellular dialysis 25033180 with the patch pipette solution containing 10 mM acacetin (the authors’ unpublished observations). Therefore, the intrinsic inactivation gating (i.e. ball and chain) of hKv4.3 channels may not be affected by acacetin. Inaddition, acacetin Lixisenatide slightly accelerated the closed-state inactivation of the channel. These are illustrated in the blocking scheme (Fig. 8). Mutagenesis experiments revealed that the inhibitory efficacy of acacetin on the hKv4.3 mutants T366A and T367A of the P-loop of the pore helix was significantly reduced. This implies that acacetin may be trapped into the channel pore and block the open channel. Moreover, the mutants V392A, I395A, and also V399A, of the S6 domain exhibit a significantly reduced response to acacetin, indicating that in addition to binding to the P-helix filter, acacetin may interact with V392, I395, and V399 of the S6 domain. Therefore, the five residues T366, T367, V392, I395, and V399 of the channel are involved in the inhibition of hKv4.3 current by acacetin. These sites are the equivalent residues of T479, T480, V505, 
I508, and V512 of hKv1.5 channels, respectively [17]. However, the blocking binding sites of acacetin for blocking Kv4.3 
channels are slightly different from those for blocking Kv1.5 channels where the P-loop helix (e.g. T480) is not involved in the binding of acacetin [17]. It is generally believed that Ito is relatively larger in the atrial cells than that in the ventricular cells, so that inhibition of Ito may cause a prolongation of repolarization predominantly in the atria more than that in the ventricle [24]. Human cardiac Ito (or Kv4.3) is considered to be a target for developing anti-atrial fibrillationAcacetin Blocks hKv4.3 ChannelsFigure 8. Blocking scheme graph shows that acacetin inhibits hKv4.3 current by interaction with different states of the channel. C, closed states; O, open states; I, inactivated states. The thickness of the arrows suggests the estimated potency of acacetin for different states of the channel. doi:10.1371/journal.pone.0057864.gdrugs [24,25]. Acacetin inhibited hKv4.3 current, especially at high frequencies. Although the blockade of hKv4.3 channels by acacetin is relatively weaker than that of hKv1.5 channels, the combination with its frequency-dependent blockade of hKv1.5/ IKur [17], favors the prolongation 1527786 of atrial action potential duration and/or effective refractory period in human atrial myocytes, which benefits for anti-atrial fibrillation. This effect has been observed in experimental canine model [16]. An increase of Ito has been found to be involved in genesis of cardiac ventricular arrhythmias or Brugada syndrome [15,26?8]. Because Ito plays a crucial role in phase 1 fast repolarization of ventricular action potentials, especially in the midmyocardium and epicardium in humans [8,12,29] and in dogs [7]. Up-regulation of Ito is involved in generation of Brugada syndrome and idiopathic ventricular fibrillation [30] by shifting cardiac repolarization and inducing J-wave syndromes that triggers the life-threatening arrhythmia [15,31]. It has been documented that an increase of Ito amplitude b.Ed by the 1st pulse of reapplied voltage steps after administration of acacetin. This property is different from that in blocking open channels of hKv1.5 [17]. The blockade of hKv4.3 and hKv1.5 channels by acacetin is likely from cytoplasmic surface, because both hKv4.3 current and hKv1.5 current were not significantly inhibited by intracellular dialysis 25033180 with the patch pipette solution containing 10 mM acacetin (the authors’ unpublished observations). Therefore, the intrinsic inactivation gating (i.e. ball and chain) of hKv4.3 channels may not be affected by acacetin. Inaddition, acacetin slightly accelerated the closed-state inactivation of the channel. These are illustrated in the blocking scheme (Fig. 8). Mutagenesis experiments revealed that the inhibitory efficacy of acacetin on the hKv4.3 mutants T366A and T367A of the P-loop of the pore helix was significantly reduced. This implies that acacetin may be trapped into the channel pore and block the open channel. Moreover, the mutants V392A, I395A, and also V399A, of the S6 domain exhibit a significantly reduced response to acacetin, indicating that in addition to binding to the P-helix filter, acacetin may interact with V392, I395, and V399 of the S6 domain. Therefore, the five residues T366, T367, V392, I395, and V399 of the channel are involved in the inhibition of hKv4.3 current by acacetin. These sites are the equivalent residues of T479, T480, V505, I508, and V512 of hKv1.5 channels, respectively [17]. However, the blocking binding sites of acacetin for blocking Kv4.3 channels are slightly different from those for blocking Kv1.5 channels where the P-loop helix (e.g. T480) is not involved in the binding of acacetin [17]. It is generally believed that Ito is relatively larger in the atrial cells than that in the ventricular cells, so that inhibition of Ito may cause a prolongation of repolarization predominantly in the atria more than that in the ventricle [24]. Human cardiac Ito (or Kv4.3) is considered to be a target for developing anti-atrial fibrillationAcacetin Blocks hKv4.3 ChannelsFigure 8. Blocking scheme graph shows that acacetin inhibits hKv4.3 current by interaction with different states of the channel. C, closed states; O, open states; I, inactivated states. The thickness of the arrows suggests the estimated potency of acacetin for different states of the channel. doi:10.1371/journal.pone.0057864.gdrugs [24,25]. Acacetin inhibited hKv4.3 current, especially at high frequencies. Although the blockade of hKv4.3 channels by acacetin is relatively weaker than that of hKv1.5 channels, the combination with its frequency-dependent blockade of hKv1.5/ IKur [17], favors the prolongation 1527786 of atrial action potential duration and/or effective refractory period in human atrial myocytes, which benefits for anti-atrial fibrillation. This effect has been observed in experimental canine model [16]. An increase of Ito has been found to be involved in genesis of cardiac ventricular arrhythmias or Brugada syndrome [15,26?8]. Because Ito plays a crucial role in phase 1 fast repolarization of ventricular action potentials, especially in the midmyocardium and epicardium in humans [8,12,29] and in dogs [7]. Up-regulation of Ito is involved in generation of Brugada syndrome and idiopathic ventricular fibrillation [30] by shifting cardiac repolarization and inducing J-wave syndromes that triggers the life-threatening arrhythmia [15,31]. It has been documented that an increase of Ito amplitude b.