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光致敏反应引起的心肌电阻滞。

The myocardial electrical blockade induced by photosensitization reaction.

机构信息

Graduate School of Science and Technology, Keio University, Yokohama 223-0061, Japan.

出版信息

IEEE Trans Biomed Eng. 2010 Feb;57(2):488-95. doi: 10.1109/TBME.2009.2031315. Epub 2009 Sep 18.

Abstract

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.

摘要

作者研究了光致敏反应诱导的细胞毒性在建立心肌组织电阻断中的应用。这种光致敏反应诱导的细胞毒性,即光动力疗法(PDT),使用氯光敏剂、替拉泊芬钠和红色(670nm)二极管激光进行。确认了 PDT 对大鼠心肌细胞的细胞毒性和对大鼠心肌组织的电阻断作用。研究了 PDT 诱导电阻断的机制。通过细胞致死性测量获得了正常大鼠心肌细胞中光致敏反应诱导的细胞毒性。离体大鼠心肌组织的体外实验证明了 PDT 可立即引起电阻断。此外,通过大鼠房室传导阻滞模型证实了 PDT 永久性电阻断的可能性。为了研究体外研究中获得的急性电阻断的机制,通过荧光 Ca2+指示剂 Fluo-4 AM 测量了大鼠心肌细胞内 Ca2+浓度的变化。在光致敏反应过程中观察到荧光强度的快速增加,以及光致敏反应后细胞形态的变化。这些结果表明,细胞膜损伤、Ca2+内流,最终导致细胞死亡是由光致敏反应引起的。光致敏反应诱导的坏死样细胞死亡可以解释 PDT 在体内对心肌组织的永久性电阻断。

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