Department of Pharmacology, Institute for Medical Sciences, Chonbuk National University Medical School, Jeonbuk 561-180, Republic of Korea.
Biol Pharm Bull. 2010;33(6):977-82. doi: 10.1248/bpb.33.977.
The voltage-gated K(+) channel Kv1.5 was expressed in Chinese hamster ovary cells, and its interaction with fluvoxamine was studied using a whole-cell patch-clamp technique. Fluvoxamine reduced Kv1.5 whole-cell currents in a reversible, concentration-dependent manner, with an IC(50) value of 2.0 microM, and a Hill coefficient of 0.7. Fluvoxamine-induced inhibition of Kv1.5 caused a time-dependent blockade without modifying the kinetics of current activation. Fluvoxamine additionally inhibited Kv1.5 in a closed/resting or nonconducting state after deactivation. Inhibition increased steeply between -30 and 0 mV, corresponding to the voltage range for channel opening. Inhibition displayed an additional voltage dependence at voltages greater than 0 mV, consistent with an electrical distance of 0.16. Fluvoxamine slowed the deactivation time course and a tail crossover phenomenon was observed when the tail currents, recorded in the presence and absence of fluvoxamine, were superimposed. Inhibition of Kv1.5 by fluvoxamine was use-dependent. These results suggest that fluvoxamine strongly inhibits Kv1.5 currents and the inhibition of Kv1.5 by fluvoxamine is mixed channel-state dependent.
电压门控钾 (K+) 通道 Kv1.5 在中华仓鼠卵巢细胞中表达,使用全细胞膜片钳技术研究了其与氟伏沙明的相互作用。氟伏沙明以可逆、浓度依赖的方式降低 Kv1.5 全细胞电流,IC50 值为 2.0 μM,Hill 系数为 0.7。氟伏沙明诱导的 Kv1.5 抑制作用引起时间依赖性阻断,而不改变电流激活的动力学。氟伏沙明在去激活后还抑制失活或非传导状态下的 Kv1.5。抑制作用在 -30 至 0 mV 之间急剧增加,与通道开放的电压范围相对应。在大于 0 mV 的电压下,抑制作用表现出额外的电压依赖性,与 0.16 的电距离一致。氟伏沙明减慢失活时间过程,当在存在和不存在氟伏沙明的情况下记录尾电流时,观察到尾电流交叉现象。氟伏沙明对 Kv1.5 的抑制作用是使用依赖性的。这些结果表明,氟伏沙明强烈抑制 Kv1.5 电流,氟伏沙明对 Kv1.5 的抑制作用是混合通道状态依赖性的。