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Featured researches published by Tetsuo Kitamura.


Journal of Pharmacological and Toxicological Methods | 2015

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

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

INTRODUCTION 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. METHODS 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. RESULTS 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. DISCUSSION 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.


Alcoholism: Clinical and Experimental Research | 2001

How Is the Liver Primed or Sensitized for Alcoholic Liver Disease

Hidekazu Tsukamoto; Yoshiyuki Takei; Craig J. McClain; Swati Joshi-Barve; Daniell B. Hill; Jack Schmidt; Ion V. Deaciuc; S Barve; Anna Colell; Carmen García-Ruiz; Neil Kaplowitz; José C. Fernández-Checa; Hirokazu Yokoyama; Yukishige Okamura; Yuji Nakamura; Hiromasa Ishii; Rajendar K. Chawla; Walter H. Watson; Wendy Nelson; Min Lin; Mitsuru Ohata; Kenta Motomura; Nobuyuki Enomoto; Kenichi Ikejima; Tetsuo Kitamura; Hirosumi Oide; Miyoko Hirose; Blair U. Bradford; Chantal A. Rivera; Hiroaki Kono


Archive | 1972

Gantry mill free from the effects of thermal deformation of a bridge member

Tetsuo Kitamura; Akira Tamai


Journal of Pharmacological and Toxicological Methods | 2016

Usefulness of motion vector prediction system for evaluating drug-induced functional changes of human induced pluripotent stem cell-derived cardiomyocytes

Masaki Honda; Akihiro Ishitomi; Yoshiko Okai; Tetsuo Kitamura; Takehito Isobe; Keiko Matsune; Seiichi Araki


Journal of Pharmacological and Toxicological Methods | 2018

Trial for data analysis of drug responses in primary rodent neurons and human-induced pluripotent stem cell-derived neurons using MEA and deep learning

Norimasa Miyamoto; Atsuko Ojima; Tetsuo Kitamura; Tomoharu Osada; Tadashi Kadowaki; Takashi Yoshinaga


Journal of Pharmacological and Toxicological Methods | 2017

Pacing of Human iPS Cell-Derived Cardiomyocytes (hiPSC-CMs) is Effective for Detecting Chronic Arrhythmogenic Risk of Pharmaceutical Compounds

Tomoharu Osada; Tetsuo Kitamura; Kimihito Yoshikawa; Fumihide Bunai; Mayumi Obo; Hideomi Uchida; Yasuyuki Onishi; Hideaki Hiratsuka; Hiroaki Inoue


Journal of Pharmacological and Toxicological Methods | 2014

Field potential measurement using iPS cell-derived cardiomyocytes for the prediction of cardiotoxicity in vitro

Mototsugu Sakakibara; Tetsuo Kitamura; Makoto Otsuki; Fumihide Bunai; Daisuke Minami; Yukiko Fujisaki; Masaru Sekijima; Tomoharu Osada


Journal of Pharmacological and Toxicological Methods | 2011

Availability of recording field potential of human stem cell-derived cardiomyocytes by multi-electrode array system

Mototsugu Sakakibara; Mikiko Koike; Tetsuo Kitamura; Minoru Tateno; Tomoharu Osada; Fumimasa Nomura; Tomoyuki Kaneko; Masaru Sekijima; Kenji Yasuda


Journal of Pharmacological and Toxicological Methods | 2010

A new in vitro model to detect proarrhythmic effects of drugs on human heart cells

Atsushi Sugiyama; Tetsuo Kitamura; Fumimasa Nomura; Tomoyuki Kaneko; Yuji Nakamura; Peter Sartipy; Kenji Yasuda


Biophysical Journal | 2010

Development of Novel System for the Functional Analysis of the Cardiomyocytes Network Model Using On-Chip Cellomics Technology

Fumimasa Nomura; Tetsuo Kitamura; Tomoyuki Kaneko; Kenji Yasuda

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Kenji Yasuda

Tokyo Medical and Dental University

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Fumimasa Nomura

Tokyo Medical and Dental University

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Kentaro Ando

Tokyo Medical and Dental University

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