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Novel non-thermal atrial fibrillation treatment with photosensitization reaction: Possibility of permanent electrical blockade in rat chronic model

机译:具有光敏反应的新型非热心房颤动治疗:大鼠慢性模型永久性电阻断的可能性

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We demonstrated a possibility of electrical conduction block by ex vivo and in vivo experiments using rat models to establish a non-thermal treatment for atrial fibrillation by photosensitization reaction (PR). One hour after the injection of 2 mg/kg Talaporfin sodium to Wistar rat, the right ventricle (1.4 mmT) was extracted. Paced with a stimulation electrode, this tissue was placed in a tissue bath and immersed in irrigated Tyrode's solution of 37°C with 8 μg/ml Talaporfin sodium and the gas mixture bubbling of 95% CO_2 and 5% O_2. The propagated electrical signal was measured by two bipolar electrodes. Exciting light of 670 nm in wavelength was irradiated to the tissue between the bipolar electrodes by the power density of 1 W/cm~2. After this irradiation, propagation signal blockade was obtained and continued up to three hours. Rat atrioventricular (AV) node was employed as a target region for chronic model. The heart of Wistar rat was surgically exposed. External four-lead electrocardiogram of this rat was measured. Thirty minutes after the injection of 10 mg/kg Talaporfin sodium to the rat, exciting light of 663 nm in wavelength was irradiated to the AV node by the power density of 500 mW/cm~2 for ten minutes. Acute AV block was obtained during the irradiation. Two weeks after this procedure, complete AV block was confirmed. The rat was sacrificed to obtain the tissue specimen. We found that the AV node was replaced by scarring tissue under the microscopic observation of the specimen. We verified possibility of permanent electrical conduction block using PR.
机译:我们通过大鼠模型通过离体和体内实验证明了建立电传导阻滞的可能性,该模型通过光敏化反应(PR)建立了非热治疗房颤的方法。向Wistar大鼠注射2 mg / kg他拉泊芬钠1小时后,提取右心室(1.4 mmT)。在刺激电极上跳动,将该组织置于组织浴中,并浸入37°C的Tyrode's溶液(含8μg/ ml Talaporfin钠)和95%CO_2和5%O_2鼓泡的气体混合物中。传播的电信号由两个双极电极测量。波长为670 nm的激发光以1 W / cm〜2的功率密度照射到双极电极之间的组织。辐照后,获得了传播信号阻断,并持续了长达三个小时。大鼠房室(AV)节点被用作慢性模型的目标区域。 Wistar大鼠的心脏通过手术暴露。测量了该大鼠的外部四导联心电图。向大鼠注射10 mg / kg他拉泊芬钠30分钟后,以500 mW / cm〜2的功率密度向AV节点照射波长为663 nm的激发光,持续10分钟。在照射过程中获得了急性AV阻滞。手术后两周,确认完全性房室传导阻滞。处死大鼠以获得组织样本。我们发现,在标本的显微镜观察下,AV结被瘢痕组织代替。我们使用PR验证了永久性电传导阻滞的可能性。

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