Shin Sung Eun, Li Hongliang, Kim Han Sol, Kim Hye Won, Seo Mi Seon, Ha Kwon-Soo, Han Eun-Taek, Hong Seok-Ho, Firth Amy L, Choi Il-Whan, Bae Young Min, Park Won Sun
Department of Physiology, Kangwon National University School of Medicine, Chuncheon 24341, Korea.
Department of Molecular and Cellular Biochemistry, Kangwon National University School of Medicine, Chuncheon 24341, Korea.
Korean J Physiol Pharmacol. 2017 Mar;21(2):225-232. doi: 10.4196/kjpp.2017.21.2.225. Epub 2017 Feb 21.
We demonstrated the effect of nortriptyline, a tricyclic antidepressant drug and serotonin reuptake inhibitor, on voltage-dependent K (Kv) channels in freshly isolated rabbit coronary arterial smooth muscle cells using a whole-cell patch clamp technique. Nortriptyline inhibited Kv currents in a concentration-dependent manner, with an apparent IC value of 2.86±0.52 µM and a Hill coefficient of 0.77±0.1. Although application of nortriptyline did not change the activation curve, nortriptyline shifted the inactivation current toward a more negative potential. Application of train pulses (1 or 2 Hz) did not change the nortriptyline-induced Kv channel inhibition, suggesting that the effects of nortiprtyline were not use-dependent. Preincubation with the Kv1.5 and Kv2.1/2.2 inhibitors, DPO-1 and guangxitoxin did not affect nortriptyline inhibition of Kv channels. From these results, we concluded that nortriptyline inhibited Kv channels in a concentration-dependent and state-independent manner independently of serotonin reuptake.
我们使用全细胞膜片钳技术,在新鲜分离的兔冠状动脉平滑肌细胞中,证明了三环类抗抑郁药和5-羟色胺再摄取抑制剂去甲替林对电压依赖性钾(Kv)通道的作用。去甲替林以浓度依赖性方式抑制Kv电流,其表观半数抑制浓度值为2.86±0.52µM,希尔系数为0.77±0.1。尽管应用去甲替林并未改变激活曲线,但去甲替林使失活电流向更负的电位移动。施加串刺激(1或2Hz)并未改变去甲替林诱导的Kv通道抑制,这表明去甲替林的作用并非使用依赖性。用Kv1.5和Kv2.1/2.2抑制剂DPO-1和广西毒素预孵育,并不影响去甲替林对Kv通道的抑制作用。根据这些结果,我们得出结论,去甲替林以浓度依赖性和状态非依赖性方式抑制Kv通道,且与5-羟色胺再摄取无关。