Kim Han Sol, Li Hongliang, Kim Hye Won, Shin Sung Eun, Jung Won-Kyo, Ha Kwon-Soo, Han Eun-Taek, Hong Seok-Ho, Firth Amy L, Choi Il-Whan, Park Won Sun
Institute of Medical Sciences, Department of Physiology, Kangwon National University School of Medicine, Chuncheon, South Korea.
Department of Biomedical Engineering and Center for Marine-Integrated Biomedical Technology (BK21 Plus), Pukyong National University, Busan, South Korea.
Clin Exp Pharmacol Physiol. 2017 Apr;44(4):480-487. doi: 10.1111/1440-1681.12723.
We investigated the inhibitory effect of dapoxetine, a selective serotonin reuptake inhibitor (SSRI), on voltage-dependent K (Kv) channels using native smooth muscle cells from rabbit coronary arteries. Dapoxetine inhibited Kv channel currents in a concentration-dependent manner, with an IC value of 2.68±0.94 μmol/L and a slope value (Hill coefficient) of 0.63±0.11. Application of 10 μmol/L dapoxetine accelerated the rate of inactivation of Kv currents. Although dapoxetine did not modify current activation kinetics, it caused a significant negative shift in the inactivation curves. Application of train step (1 or 2 Hz) progressively increased the inhibitory effect of dapoxetine on Kv channels. In addition, the recovery time constant was extended in its presence, suggesting that the longer recovery time constant from inactivation underlies a use-dependent inhibition of the channel. From these results, we conclude that dapoxetine inhibits Kv channels in a dose-, time-, use-, and state (open)-dependent manner, independent of serotonin reuptake inhibition.
我们使用来自兔冠状动脉的天然平滑肌细胞,研究了选择性5-羟色胺再摄取抑制剂(SSRI)达泊西汀对电压依赖性钾(Kv)通道的抑制作用。达泊西汀以浓度依赖性方式抑制Kv通道电流,其半数抑制浓度(IC)值为2.68±0.94 μmol/L,斜率值(希尔系数)为0.63±0.11。应用10 μmol/L达泊西汀可加速Kv电流的失活速率。虽然达泊西汀未改变电流激活动力学,但它使失活曲线发生显著负向位移。应用串刺激(1或2 Hz)可逐渐增强达泊西汀对Kv通道的抑制作用。此外,在其存在的情况下,恢复时间常数延长,这表明失活后较长的恢复时间常数是该通道使用依赖性抑制的基础。从这些结果中,我们得出结论,达泊西汀以剂量、时间、使用和状态(开放)依赖性方式抑制Kv通道,与5-羟色胺再摄取抑制无关。