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光敏化反应诱导的心肌组织电传导阻滞

Photosensitization reaction-induced electrical blockade in myocardial tissue.

作者信息

Ito A, Hosokawa S, Miyoshi S, Soejima K, Arai T

机构信息

School of Fundamental Science and Technology, Graduate School of Science and Technology, Keio University, Japan.

出版信息

Annu Int Conf IEEE Eng Med Biol Soc. 2008;2008:4361-3. doi: 10.1109/IEMBS.2008.4650176.

Abstract

We proposed the application of photodynamic therapy (PDT) as a new type of atrial fibrillation treatment. PDT is well known as a practical cancer treatment using cytotoxicity of reactive oxygen species generated by the photochemical interaction. We predicted that the photocytotoxic effect induced by PDT might cause electrical blockade in myocardial tissue. We studied the electrical blockade induced by the PDT with talaporfin sodium in vitro, ex vivo, and in vivo. The cell lethality measurement using rat cardiac myocytes confirmed the PDT-induced photocytotoxic effect and its dependence on the loading time of the photosensitizer. In ex vivo experiment using rat right ventricle, the PDT caused a shutdown of the stimulated electrical signal propagation. The long-lasting atrioventricular block induced by the PDT was obtained in vivo experiment with rat heart. These results revealed the possibility of atrial fibrillation treatment with the PDT.

摘要

我们提出将光动力疗法(PDT)应用于新型心房颤动治疗。光动力疗法作为一种利用光化学相互作用产生的活性氧的细胞毒性的实用癌症治疗方法而广为人知。我们预测光动力疗法诱导的光细胞毒性作用可能导致心肌组织电传导阻滞。我们在体外、离体和体内研究了用替拉泊芬钠进行光动力疗法诱导的电传导阻滞。使用大鼠心肌细胞进行的细胞杀伤力测量证实了光动力疗法诱导的光细胞毒性作用及其对光敏剂加载时间的依赖性。在使用大鼠右心室的离体实验中,光动力疗法导致刺激电信号传播中断。在大鼠心脏的体内实验中获得了光动力疗法诱导的持久性房室传导阻滞。这些结果揭示了用光动力疗法治疗心房颤动的可能性。

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