首页> 外文期刊>International Journal of Radiation Biology: Covering the Physical, Chemical, Biological, and Medical Effects of Ionizing and Non-ionizing Radiations >The effect of radiation dose on the onset and progression of radiation-induced brain necrosis in the rat model
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The effect of radiation dose on the onset and progression of radiation-induced brain necrosis in the rat model

机译:辐射剂量对大鼠模型辐射诱导脑坏死发作和进展的影响

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Purpose: To provide a comprehensive understanding of how the selection of radiation dose affects the temporal and spatial progression of radiation-induced necrosis in the rat model.Materials and methods: Necrosis was induced with a single fraction of radiation exposure, at doses ranging between 20 and 60Gy, to the right hemisphere of 8-week-old Fischer rats from a linear accelerator. The development and progression of necrosis in the rats was monitored and quantified every other week with T1- and T2-weighted gadolinium contrast-enhanced MRI studies.Results: The time to onset of necrosis was found to be dose-dependent, but after the initial onset, the necrosis progression rate and total volume generated was constant across different doses ranging between 30 and 60Gy. Radiation doses less than 30Gy did not develop necrosis within 33 weeks after treatment, indicating a dose threshold existing between 20 and 30Gy.Conclusion: The highest dose used in this study led to the shortest time to onset of radiation-induced necrosis, while producing comparable disease progression dynamics after the onset. Therefore, for the radiation-induced necrosis rat model using a linear accelerator, the most optimum results were generated from a dose of 60Gy.
机译:目的:为了全面了解辐射剂量选择如何影响大鼠模型中辐射诱导的坏死的时间和空间进展。材料和方法:用单一的辐射曝光诱导坏死,剂量在20之间和60Gy,到来自线性加速器的8周龄Fischer大鼠的右半球。大鼠中坏死的发育和进展每隔一周监测和量化,用T1和T2加权钆对比增强的MRI研究。结果:发现坏死的发生时间是依赖的,但在初始之后发病,在30到60Gy之间的不同剂量范围内,产生的坏死进展率和产生的总体积是恒定的。辐射剂量小于30Gy的治疗后33周内没有发育坏死,表明存在于20至30Gy之间的剂量阈值。结论:本研究中使用的最高剂量导致了辐射诱导的坏死的最短时间,同时产生可比性发病后疾病进展动态。因此,对于使用线性加速器的辐射诱导的坏死大鼠模型,从60Gy的剂量产生最佳结果。

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