TY - GEN
T1 - Photosensitization reaction-induced electrophysiological response of myocardial cells dependent on subcellular photosensitizer distribution
AU - Ito, A.
AU - Matsuo, H.
AU - Suenari, T.
AU - Kimura, T.
AU - Miyoshi, S.
AU - Ogawa, S.
AU - Arai, Tsunenori
PY - 2009
Y1 - 2009
N2 - We have demonstrated photosensitization reaction-induced electrical conduction block of myocardial tissue. Subcellular distribution of photosensitizer and electrophysiological cell response to this photosensitization reaction were studied with rat myocardial cells, in order to clarify the mechanism of the myocardial electrical conduction block with photodynamic therapy (PDT). Photofrin® was used as photo sensitizer in this study. The subcellular distribution of the photosensitizer was obtained by microscopic fluorescent observation. The sites of photosensitizer localization were deter mined by organelle fluorescent probe, Rhodamine® 123, to specify the mitochondria location. The myocardial cell response to the photosensitization reaction was studied by the observation of intracellular Ca2+ dynamics. Intracellular free Ca2+concentration in the myocardial cells was measured with fluorescent Ca2+ indicator, Fluo-4 AM, by a high-speed Nipkow type confocal laser microscope during the PDT when the photosensitizer was distributed outside the cells or localized to intracellular compartments. We concluded that the Ca2+ influx accompanied by cell membrane damage when the photosensitizer was distributed outside the cells or on the cell membrane was the possible mechanism of the myocardial electrical conduction block with the photosensitization reaction.
AB - We have demonstrated photosensitization reaction-induced electrical conduction block of myocardial tissue. Subcellular distribution of photosensitizer and electrophysiological cell response to this photosensitization reaction were studied with rat myocardial cells, in order to clarify the mechanism of the myocardial electrical conduction block with photodynamic therapy (PDT). Photofrin® was used as photo sensitizer in this study. The subcellular distribution of the photosensitizer was obtained by microscopic fluorescent observation. The sites of photosensitizer localization were deter mined by organelle fluorescent probe, Rhodamine® 123, to specify the mitochondria location. The myocardial cell response to the photosensitization reaction was studied by the observation of intracellular Ca2+ dynamics. Intracellular free Ca2+concentration in the myocardial cells was measured with fluorescent Ca2+ indicator, Fluo-4 AM, by a high-speed Nipkow type confocal laser microscope during the PDT when the photosensitizer was distributed outside the cells or localized to intracellular compartments. We concluded that the Ca2+ influx accompanied by cell membrane damage when the photosensitizer was distributed outside the cells or on the cell membrane was the possible mechanism of the myocardial electrical conduction block with the photosensitization reaction.
KW - Electrical conduction block
KW - Photodynamic therapy
KW - Photofrin®
KW - Photosensitization reaction
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U2 - 10.1007/978-3-642-03885-3_64
DO - 10.1007/978-3-642-03885-3_64
M3 - Conference contribution
AN - SCOPUS:77949785722
SN - 9783642038846
T3 - IFMBE Proceedings
SP - 229
EP - 231
BT - World Congress on Medical Physics and Biomedical Engineering
PB - Springer Verlag
T2 - World Congress on Medical Physics and Biomedical Engineering: Diagnostic and Therapeutic Instrumentation, Clinical Engineering
Y2 - 7 September 2009 through 12 September 2009
ER -