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Am J Physiol Cell Physiol 289: C425-C436, 2005. First published March 30, 2005; doi:10.1152/ajpcell.00450.2004
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MEMBRANE TRANSPORTERS, ION CHANNELS, AND PUMPS

Direct block of cloned hKv1.5 channel by cytochalasins, actin-disrupting agents

Bok Hee Choi,1 Jung-Ah Park,1 Kyung-Ryoul Kim,1 Ggot-Im Lee,1 Yong-Tae Lee,1 Huhn Choe,2 Seong-Hoon Ko,2 Min-Ho Kim,3 Yeon-Ho Seo,3 and Yong-Geun Kwak1

Departments of 1Pharmacology, 2Anesthesiology, and 3Thoracic and Cardiovascular Surgery, Chonbuk National University Medical School, Chonju, Chonbuk, Republic of Korea

Submitted 13 September 2004 ; accepted in final form 25 March 2005

The action of cytochalasins, actin-disrupting agents on human Kv1.5 channel (hKv1.5) stably expressed in Ltk cells was investigated using the whole cell patch-clamp technique. Cytochalasin B inhibited hKv1.5 currents rapidly and reversibly at +60 mV in a concentration-dependent manner with an IC50 of 4.2 µM. Cytochalasin A, which has a structure very similar to cytochalasin B, inhibited hKv1.5 (IC50 of 1.4 µM at +60 mV). Pretreatment with other actin filament disruptors cytochalasin D and cytochalasin J, and an actin filament stabilizing agent phalloidin had no effect on the cytochalasin B-induced inhibition of hKv1.5 currents. Cytochalasin B accelerated the decay rate of inactivation for the hKv1.5 currents. Cytochalasin B-induced inhibition of the hKv1.5 channels was voltage dependent with a steep increase over the voltage range of the channel's opening. However, the inhibition exhibited voltage independence over the voltage range in which channels are fully activated. Cytochalasin B produced no significant effect on the steady-state activation or inactivation curves. The rate constants for association and dissociation of cytochalasin B were 3.7 µM/s and 7.5 s–1, respectively. Cytochalasin B produced a use-dependent inhibition of hKv1.5 current that was consistent with the slow recovery from inactivation in the presence of the drug. Cytochalasin B (10 µM) also inhibited an ultrarapid delayed rectifier K+ current (IK,ur) in human atrial myocytes. These results indicate that cytochalasin B primarily blocks activated hKv1.5 channels and endogenous IK,ur in a cytoskeleton-independent manner as an open-channel blocker.

voltage-gated K+ channel; heart; open channel block



Address for reprint requests and other correspondence: Y.-G. Kwak, Dept. of Pharmacology, Chonbuk National Univ. Medical School, Chonju, Chonbuk 561-180, Republic of Korea (e-mail: ygkwak{at}chonbuk.ac.kr)







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