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高温治疗期间EMT-6肿瘤的非侵入性体内电阻抗:与形态学及肿瘤生长延迟的相关性

Non-invasive, in-vivo electrical impedance of EMT-6 tumours during hyperthermia: correlation with morphology and tumour-growth-delay.

作者信息

McRae D A, Esrick M A, Mueller S C

机构信息

Department of Radiation Medicine, Georgetown University, Washington, D.C. 20057, USA.

出版信息

Int J Hyperthermia. 1997 Jan-Feb;13(1):1-20. doi: 10.3109/02656739709056426.

Abstract

The electrical impedance at frequencies from 100 Hz to 40 MHz of EMT-6 tumours was measured non-invasively, in vivo, during hyperthermia using an apparatus constructed for this purpose. Histology and morphometry were performed on tumours harvested periodically during the heating. A ratio of conductivities at two frequencies (sigma (10MHz)/sigma (10kHz)), which minimizes the tissues temperature-coefficient effects, was used to correlate impedance changes with the histopathological changes. The bulk of the cell population followed a necrotic cell death sequence during heating. Initial increase of the sigma-ratio correlated with cell swelling, and a reversal of the rate of this increase correlated with the appearance of small membrane breaks and evidence of mitochondrial damage. A continued, slowing sigma-ratio increase to a maximum correlated with continued cell swelling accompanied by increasing membrane disruption. The subsequent decrease in sigma-ratio correlated with continued general cell lysing. Between the appearance of the first membrane breaks (sigma-ratio peak) and the evidence of general lysing (sigma-ratio peak), the tumour-growth-delay increased non-linearly. Because the sigma-ratio consistently discerned these events, these measurements were able to predict the fate of this cell population when subjected to hyperthermia. Knowledge of temperature or time of heating was not required.

摘要

使用为此目的构建的仪器,在热疗期间对EMT - 6肿瘤在100 Hz至40 MHz频率下的电阻抗进行了体内非侵入性测量。在加热过程中定期采集的肿瘤上进行组织学和形态测量。使用两个频率下的电导率之比(σ(10MHz)/σ(10kHz)),该比值可使组织温度系数效应最小化,用于将阻抗变化与组织病理学变化相关联。在加热过程中,大部分细胞群体遵循坏死性细胞死亡序列。σ比值的初始增加与细胞肿胀相关,而该增加速率的逆转与小的膜破裂的出现和线粒体损伤的证据相关。σ比值持续缓慢增加至最大值与持续的细胞肿胀以及膜破坏增加相关。随后σ比值的下降与持续的总体细胞溶解相关。在第一次膜破裂出现(σ比值峰值)和总体溶解证据(σ比值峰值)之间,肿瘤生长延迟呈非线性增加。由于σ比值始终能够识别这些事件,这些测量能够预测该细胞群体在热疗时的命运。不需要知道加热温度或时间。

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