Calcium Channel Inhibitor, Verapamil, Inhibits the Voltage-Dependent K+ Channels in Rabbit Coronary Smooth Muscle Cellsopen access
- Authors
- Ko, Eun A.; Park, Won Sun; Son, Youn Kyoung; Ko, Jae-Hong; Choi, Tae-Hoon; Jung, In Duk; Park, Yeong-Min; Hong, Da Hye; Kim, Nari; Han, Jin
- Issue Date
- Jan-2010
- Publisher
- PHARMACEUTICAL SOC JAPAN
- Keywords
- verapamil; voltage-dependent K+ channel; coronary arterial smooth muscle cell
- Citation
- BIOLOGICAL & PHARMACEUTICAL BULLETIN, v.33, no.1, pp 47 - 52
- Pages
- 6
- Journal Title
- BIOLOGICAL & PHARMACEUTICAL BULLETIN
- Volume
- 33
- Number
- 1
- Start Page
- 47
- End Page
- 52
- URI
- https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/22712
- DOI
- 10.1248/bpb.33.47
- ISSN
- 0918-6158
1347-5215
- Abstract
- We investigated the effect of the phenylalkylamine Ca2+ channel inhibitor verapamil on voltage-dependent K+ (Kv) channels in rabbit coronary arterial smooth muscle cells using a whole-cell patch clamp technique. Verapamil reduced the Kv current amplitude in a concentration-depenent manner. The apparent K-d value for Kv channel inhibition was 0.82 mu m. Although verapamil had no effect on the activation kinetics, it accelerated the decay rate of Kv channel inactivation. The rate constants of association and dissociation by verapamil were 2.20 +/- 0.02 mu M-1 s(-1), and 1.79 +/- 0.26 s(-1), respectively. The steady-state activation and inactivation curves were unaffected by verapamil. The application of train pulses increased the verapamil-induced Kv channel inhibition. Furthermore, verapamil increased the recovery time constant, suggesting that the inhibitory effect of this agent was use-dependent. The inhibitory effect of verapamil was not affected by intracellular and extracellular Ca2+-free conditions. Another Ca2+ channel inhibitor, nifedipine (10 mu m) did not affect the Kv current, and did not alter the inhibitory effect of verapamil. Based on these results, we concluded that verapamil inhibited Kv current in a state-, time-, and use-dependent manner, independent of Ca2+ channel inhibition.
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