TY - JOUR
T1 - The Myocardial Electrical Blockade Induced by Photosensitization Reaction
AU - Ito, Arisa
AU - Hosokawa, Shuntaro
AU - Arai, Tsunenori
AU - Miyoshi, Shunichiro
AU - Soejima, Kyoko
AU - Ogawa, Satoshi
N1 - Funding Information:
Manuscript received September 30, 2008; revised March 2, 2009 and July 26, 2009. First published September 18, 2009; current version published January 20, 2010. This work was supported in part by the Supporting Program for Creating University Ventures (#1904) of the Japan Science and Technology Agency. Asterisk indicates corresponding author.
PY - 2010/2
Y1 - 2010/2
N2 - The authors studied the application of photosensitization-reaction-induced cytotoxicity to establish electrical blockade of myocardial tissue. This photosensitization-reaction-induced cytotoxicity, i.e., photodynamic therapy (PDT) was performed with chlorine photosensitizer, talaporfin sodium, and a red (670 nm) diode laser. The cytotoxicity on rat cardiac myocytes and the electrical blockade by PDT using rat myocardial tissue were confirmed. The mechanism of PDT-induced electrical blockade was investigated. The photosensitization-reaction-induced cytotoxicity in normal rat cardiac myocytes was obtained in cell lethality measurement. The ex vivo experiment with rat-isolated myocardial tissue demonstrated the immediate electrical blockade by PDT. Moreover, the possibility of permanent electrical blockade by PDT using rat atrioventricular blockade model was confirmed. To study the mechanism of the acute electrical blockade obtained in the ex vivo study, intracellular Ca2+ concentration changes in rat cardiac myocytes were measured by the intensity of the fluorescent Ca2+ indicator Fluo-4 AM. A rapid increase in fluorescence intensity during the photosensitization reaction and a change in cell morphology after the photosensitization reaction were observed. These results indicate that cell membrane damage, Ca2+ influx, and eventually cell death are caused by the photosensitization reaction. The necrosis-like cell death induced by the photosensitization reaction can explain a permanent electrical blockade of the myocardial tissue in vivo by PDT.
AB - The authors studied the application of photosensitization-reaction-induced cytotoxicity to establish electrical blockade of myocardial tissue. This photosensitization-reaction-induced cytotoxicity, i.e., photodynamic therapy (PDT) was performed with chlorine photosensitizer, talaporfin sodium, and a red (670 nm) diode laser. The cytotoxicity on rat cardiac myocytes and the electrical blockade by PDT using rat myocardial tissue were confirmed. The mechanism of PDT-induced electrical blockade was investigated. The photosensitization-reaction-induced cytotoxicity in normal rat cardiac myocytes was obtained in cell lethality measurement. The ex vivo experiment with rat-isolated myocardial tissue demonstrated the immediate electrical blockade by PDT. Moreover, the possibility of permanent electrical blockade by PDT using rat atrioventricular blockade model was confirmed. To study the mechanism of the acute electrical blockade obtained in the ex vivo study, intracellular Ca2+ concentration changes in rat cardiac myocytes were measured by the intensity of the fluorescent Ca2+ indicator Fluo-4 AM. A rapid increase in fluorescence intensity during the photosensitization reaction and a change in cell morphology after the photosensitization reaction were observed. These results indicate that cell membrane damage, Ca2+ influx, and eventually cell death are caused by the photosensitization reaction. The necrosis-like cell death induced by the photosensitization reaction can explain a permanent electrical blockade of the myocardial tissue in vivo by PDT.
KW - Electrical blockade
KW - photodynamic therapy (PDT)
KW - photosensitization reaction
KW - photosensitizer
KW - talaporfin sodium
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U2 - 10.1109/TBME.2009.2031315
DO - 10.1109/TBME.2009.2031315
M3 - Article
C2 - 19770088
AN - SCOPUS:77950366127
SN - 0018-9294
VL - 57
SP - 488
EP - 495
JO - IEEE Transactions on Biomedical Engineering
JF - IEEE Transactions on Biomedical Engineering
IS - 2
ER -