Qi Zhi-Ping, Shi Shan-Shan, Zhao Xue-Ling, Zhao Wen-Xiao, Bai Yun-Long, Lü Yan-Jie, Li Bao-Xin, Yang Bao-Feng
Department of Pharmacology, Bio-pharmaceutical Key Laboratory of Heilongjiang Province-Incubator of State Key Laboratory, Harbin Medical University, Harbin 150086, China.
Yao Xue Xue Bao. 2008 Jan;43(1):44-9.
Human ether-a-go-go-related gene (HERG) encodes the rapid component of the cardiac delayed rectifier K+ current, which has an important effect on both proarrhythmia and antiarrhythmia. To investigate the effect of sophocarpine (SC) on HERG channel stably expressing in human embryonic kidney-293 (HEK293) cells, whole-cell patch-clamp technique was used to record HERG current and kinetic curves. As the result, it was found that SC inhibited HERG current in a concentration-dependent manner (10, 30, 100, and 300 micromol x L(-1)). At 0 mV, 10, 30, 100, and 300 micromol x L(-1) SC respectively inhibited IHERG by Istep ( 10.7 +/- 2.8)% , (11.3 +/- 5.5)% , (47.0 +/- 2.3)% and (53.7 +/- 2.5)% , and Itail (1.1 +/- 3.0)%, (17.1 +/- 3.3)%, (32.7 +/- 1.9)% (P < 0.05, n = 12) and (56.0 +/- 2.4)% (P < 0.05, n = 13). The time constants of inactivation, recovery from inactivation and onset of inactivation were accelerated. SC did not change other channel kinetics (activation and deactivation). It is concluded that SC inhibited the transfected HERG channels by influencing the inactivation state, which is the probable anti-arrhythmic mechanism.
人醚 - 去极化相关基因(HERG)编码心脏延迟整流钾电流的快速成分,这对致心律失常和抗心律失常都有重要作用。为研究槐果碱(SC)对在人胚肾 - 293(HEK293)细胞中稳定表达的HERG通道的影响,采用全细胞膜片钳技术记录HERG电流和动力学曲线。结果发现,SC以浓度依赖性方式抑制HERG电流(10、30、100和300 μmol·L⁻¹)。在0 mV时,10、30、100和300 μmol·L⁻¹的SC分别使IHERG的阶跃电流抑制(10.7±2.8)%、(11.3±5.5)%、(47.0±2.3)%和(53.7±2.5)%,尾电流抑制(1.1±3.0)%、(17.1±3.3)%、(32.7±1.9)%(P<0.05,n = 12)和(56.0±2.4)%(P<0.05,n = 13)。失活时间常数、从失活恢复的时间常数和失活起始时间常数均加快。SC未改变其他通道动力学(激活和去激活)。结论是,SC通过影响失活状态抑制转染的HERG通道,这可能是其抗心律失常机制。