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超声照射的EMT6小鼠乳腺肉瘤细胞中胸腺嘧啶碱基损伤的产生。

Production of thymine base damage in ultrasound-exposed EMT6 mouse mammary sarcoma cells.

作者信息

Dooley D A, Sacks P G, Miller M W

出版信息

Radiat Res. 1984 Jan;97(1):71-86.

PMID:6695045
Abstract

Mouse mammary sarcoma cells, line EMT6/Ro, were exposed for 1 min to 1 MHz continuous wave ultrasound over a range of intensities from 0.5 to 30 W/cm2 (spatial peak). The presence of thymine base damage (TBD) products of the 5,6-dihydroxydihydrothymine type was determined by an alkali degradation assay. Production of damage was found to be greatest (approximately 2.7 X 10(-3%) t'/T) at an intensity of 10 W/cm2 and fell off rapidly above and below this intensity. The amount of base damage produced at 10 W/cm2 ultrasound was approximately equivalent to the damage produced by a gamma-ray absorbed dose of 12 krad. Assay of cells immediately after sonication at 10 W/cm2 showed that approximately 14% of the cells had been lysed. Tests showed that it was the DNA of the intact cells, however, which sustained all of the TBD. Survival data demonstrated that of the remaining unlysed cell population approximately 5% were viable, whereas cells exposed to 12 krad showed no survival. Additionally, cells were exposed for up to 5 min at 5 W/cm2. An increase in TBD was demonstrated with increasing time of exposure such that the rate of production at 5 min was approximately three times greater than that of a 1-min exposure. TBD was found to be completely suppressed when cells were sonicated at 10 W/cm2 for 2 min under 4 bar of hydrostatic pressure. Addition of the radical scavengers beta-MEA and cystamine eliminated TBD but had minimal effect on survival. The pressure and scavenger experiments demonstrate that TBD results from cavitation-induced free radicals. Based on the values for both the half-life and diffusion distance of such radicals, our results indicate that at least part of the bubble collapse occurs intracellularly.

摘要

将小鼠乳腺肉瘤细胞系EMT6/Ro,在强度范围为0.5至30W/cm²(空间峰值)的1MHz连续波超声下暴露1分钟。通过碱降解试验确定5,6 - 二羟基二氢胸腺嘧啶类型的胸腺嘧啶碱基损伤(TBD)产物的存在。发现在10W/cm²强度下损伤产生量最大(约2.7×10⁻³%t'/T),在此强度之上和之下损伤量迅速下降。10W/cm²超声产生的碱基损伤量大约相当于12kradγ射线吸收剂量产生的损伤。在10W/cm²超声处理后立即对细胞进行检测表明,约14%的细胞已被裂解。然而,测试表明,是完整细胞的DNA承受了所有的TBD。存活数据表明,在剩余未裂解的细胞群体中,约5%是存活的,而暴露于12krad的细胞则无存活。此外,细胞在5W/cm²下暴露长达五分钟。随着暴露时间增加,TBD增加,使得5分钟时的产生速率大约是1分钟暴露时的三倍。当细胞在4巴静水压力下于10W/cm²超声处理2分钟时,发现TBD被完全抑制。添加自由基清除剂β - MEA和胱胺消除了TBD,但对存活影响最小。压力和清除剂实验表明,TBD是由空化诱导的自由基产生的。基于此类自由基的半衰期和扩散距离值,我们的结果表明,至少部分气泡崩溃发生在细胞内。

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