Improvement of acquisition and analysis methods in multi-electrode array experiments with iPS cell-derived cardiomyocytes

电生理学 波形 化学 电极 电极阵列 特非那定 分析化学(期刊) 生物医学工程 材料科学 电压 色谱法 医学 药理学 内科学 物理 物理化学 量子力学
作者
Keiichi Asakura,Seiji Hayashi,Atsuko Ojima,Tomohiko Taniguchi,Norimasa Miyamoto,Chiaki Nakamori,Chiho Nagasawa,Tetsuo Kitamura,Tomoharu Osada,Yayoi Honda,Chieko Kasai,Hiroyuki Ando,Yasunari Kanda,Yuko Sekino,Kohei Sawada
出处
期刊:Journal of Pharmacological and Toxicological Methods [Elsevier]
卷期号:75: 17-26 被引量:123
标识
DOI:10.1016/j.vascn.2015.04.002
摘要

Multi-electrode array (MEA) systems and human induced pluripotent stem (iPS) cell-derived cardiomyocytes are frequently used to characterize the electrophysiological effects of drug candidates for the prediction of QT prolongation and proarrhythmic potential. However, the optimal experimental conditions for obtaining reliable experimental data, such as high-pass filter (HPF) frequency and cell plating density, remain to be determined.Extracellular field potentials (FPs) were recorded from iPS cell-derived cardiomyocyte sheets by using the MED64 and MEA2100 multi-electrode array systems. Effects of HPF frequency (0.1 or 1Hz) on FP duration (FPD) were assessed in the presence and absence of moxifloxacin, terfenadine, and aspirin. The influence of cell density on FP characteristics recorded through a 0.1-Hz HPF was examined. The relationship between FP and action potential (AP) was elucidated by simultaneous recording of FP and AP using a membrane potential dye.Many of the FP waveforms recorded through a 1-Hz HPF were markedly deformed and appeared differentiated compared with those recorded through a 0.1-Hz HPF. The concentration-response curves for FPD in the presence of terfenadine reached a steady state at concentrations of 0.1 and 0.3μM when a 0.1-Hz HPF was used. In contrast, FPD decreased at a concentration of 0.3μM with a characteristic bell-shaped concentration-response curve when a 1-Hz HPF was used. The amplitude of the first and second peaks in the FP waveform increased with increasing cell plating density. The second peak of the FP waveform roughly coincided with AP signal at 50% repolarization, and the negative deflection at the second peak of the FP waveform in the presence of E-4031 corresponded to early afterdepolarization and triggered activity.FP can be used to assess the QT prolongation and proarrhythmic potential of drug candidates; however, experimental conditions such as HPF frequency are important for obtaining reliable data.
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