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Acute cell death rate of vascular smooth muscle cells during or after short heating up to 20 s ranging 50 to 60℃ as a basic study of thermal angioplasty

机译:作为热血管成形术的基础研究,在短短的加热过程中或短时间加热至20 s或50到60℃时,血管平滑肌细胞的急性细胞死亡率

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摘要

We studied the relations between the time history of smooth muscle cells (SMCs) death rate and heating condition in vitro to clarify cell death mechanism in heating angioplasty, in particular under the condition in which intimal hyperplasia growth had been prevented in vivo swine experiment. A flow heating system on the microscope stage was used for the SMCs death rate measurement during or after the heating. The cells were loaded step-heating by heated flow using a heater equipped in a Photo-thermo dynamic balloon. The heating temperature was set to 37, 50-60℃. The SMCs death rate was calculated by a division of PI stained cell number by Hoechst33342 stained cell number. The SMCs death rate increased 5-10% linearly during 20 s with the heating. The SMCs death rate increased with duration up to 15 min after 5 s heating. Because fragmented nuclei were observed from approximately 5 min after the heating, we defined that acute necrosis and late necrosis were corresponded to within 5 min after the heating and over 5 min after the heating, respectively. This late necrosis is probably corresponding to apoptosis. The ratio of necrotic interaction divided the acute necrosis rate by the late necrosis was calculated based on this consideration as 1.3 under the particular condition in which intimal hyperplasia growth was prevented in vivo previous porcine experiment. We think that necrotic interaction rate is larger than expected rate to obtain intimal hyperplasia suppression.
机译:我们研究了平滑肌细胞(SMCs)的死亡率的时间历史与体外加热条件之间的关系,以阐明加热血管成形术中的细胞死亡机制,特别是在体内猪实验中防止内膜增生生长的情况下。显微镜载物台上的流动加热系统用于加热期间或加热后SMC的死亡率测量。使用装备在光热动态气球中的加热器通过加热流对电池进行分步加热。加热温度设定为37,50-60℃。通过PI染色的细胞数除以Hoechst33342染色的细胞数来计算SMC的死亡率。随着加热,SMC的死亡率在20 s内线性增加5-10%。加热5秒后,SMC的死亡率随着持续时间的增加而增加,持续时间长达15分钟。由于加热后约5分钟观察到细胞核碎裂,我们定义急性坏死和晚期坏死分别对应于加热后5分钟内和加热后5分钟以上。晚期坏死可能对应于细胞凋亡。基于这种考虑,在特定的条件下,在体内先前的猪实验中阻止了内膜增生的生长,坏死相互作用的比率除以急性坏死率除以晚期坏死的比率为1.3。我们认为坏死的相互作用速率大于预期的内膜增生抑制率。

著录项

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  • 会议地点 San Francisco CA(US)
  • 作者单位

    School of Fundamental Science and Technology, Graduate School of Science and Technology, Keio University, 3-14-1, Hiyoshi, Kohoku-ku, Yokohama City, Kanagawa, 223-8522, Japan;

    School of Fundamental Science and Technology, Graduate School of Science and Technology, Keio University, 3-14-1, Hiyoshi, Kohoku-ku, Yokohama City, Kanagawa, 223-8522, Japan;

    School of Fundamental Science and Technology, Graduate School of Science and Technology, Keio University, 3-14-1, Hiyoshi, Kohoku-ku, Yokohama City, Kanagawa, 223-8522, Japan;

    School of Fundamental Science and Technology, Graduate School of Science and Technology, Keio University, 3-14-1, Hiyoshi, Kohoku-ku, Yokohama City, Kanagawa, 223-8522, Japan;

    School of Fundamental Science and Technology, Graduate School of Science and Technology, Keio University, 3-14-1, Hiyoshi, Kohoku-ku, Yokohama City, Kanagawa, 223-8522, Japan;

  • 会议组织
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    smooth muscle cell (SMC); short heating; necrosis; apoptosis; intimal hyperplasia;

    机译:平滑肌细胞(SMC);加热时间短坏死细胞凋亡内膜增生;
  • 入库时间 2022-08-26 13:44:41

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