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色满醇293B对人心房肌细胞瞬时外向和超快速延迟整流钾电流的影响。

Effects of chromanol 293B on transient outward and ultra-rapid delayed rectifier potassium currents in human atrial myocytes.

作者信息

Du Xin-Ling, Lau Chu-Pak, Chiu Shui-Wah, Tse Hung-Fat, Gerlach Uwe, Li Gui-Rong

机构信息

Institute of Cardiovascular Science and Medicine, Department of Medicine, University of Hong Kong, SAR, Hong Kong, China.

出版信息

J Mol Cell Cardiol. 2003 Mar;35(3):293-300. doi: 10.1016/s0022-2828(03)00007-5.

Abstract

It is unclear whether chromanol 293B, a selective inhibitor of slow component of delayed rectifier K(+) current (I(Ks)), may affect other K(+) currents in human atrium. With whole-cell patch configuration, we evaluated effects of 293B on transient outward K(+) current (I(to1)) and ultra-rapid delayed rectifier K(+) current (I(Kur)) in isolated human atrial myocytes. It was found that 293B inhibited I(to1) and I(Kur) in a concentration-dependent manner. At 10 microM 293B suppressed I(to1) to 3.4 +/- 0.4 from 5.1 +/- 0.3 pA/pF (P < 0.01), and I(Kur) to 1.5 +/- 0.2 from 2.1 +/- 0.3 pA/pF (P < 0.01) at +50 mV. The inhibition of I(to1) and I(Kur) was independent of depolarizing voltage, and the concentration of 50% inhibition was 31.2 microM for I(to1), and 30.9 microM for I(Kur). 293B blocked I(to1) and I(Kur) with the same concentration range, and the significant effect was observed from the concentration of 1 microM. The maximum inhibitive effect was 88% for I(to1) and 96% for I(Kur) at 250 microM. Voltage dependence of activation and inactivation, and time-dependent recovery from inactivation of I(to1) were not altered by 293B; however, time to peak and time-dependent inactivation of I(to1) was significantly accelerated. The results indicate that 293B significantly inhibits the major repolarization K(+) currents I(to1) and I(Kur) in human atrial myocytes.

摘要

尚不清楚延迟整流钾电流慢成分(I(Ks))的选择性抑制剂色满醇293B是否会影响人心房中的其他钾电流。采用全细胞膜片钳记录模式,我们评估了293B对分离的人心房肌细胞瞬时外向钾电流(I(to1))和超快速延迟整流钾电流(I(Kur))的影响。结果发现,293B以浓度依赖性方式抑制I(to1)和I(Kur)。在10 μM时,293B将+50 mV时的I(to1)从5.1±0.3 pA/pF抑制至3.4±0.4 pA/pF(P<0.01),将I(Kur)从2.1±0.3 pA/pF抑制至1.5±0.2 pA/pF(P<0.01)。I(to1)和I(Kur)的抑制与去极化电压无关,I(to1)的50%抑制浓度为31.2 μM,I(Kur)为30.9 μM。293B在相同浓度范围内阻断I(to1)和I(Kur),在1 μM浓度时即可观察到显著作用。在250 μM时,I(to1)的最大抑制作用为88%,I(Kur)为96%。293B未改变I(to1)的激活和失活电压依赖性以及失活后的时间依赖性恢复;然而,I(to1)的峰值时间和时间依赖性失活显著加快。结果表明,293B显著抑制人心房肌细胞中的主要复极化钾电流I(to1)和I(Kur)。

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