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非常规放疗方案下小鼠口腔黏膜的再增殖反应

Repopulation response of mouse oral mucosa during unconventional radiotherapy protocols.

作者信息

Dörr W, Weber-Frisch M

机构信息

GSF-Institut für Strahlenbiologie, Oberschleissheim, Germany.

出版信息

Radiother Oncol. 1995 Dec;37(3):230-6. doi: 10.1016/0167-8140(95)01666-x.

Abstract

Repopulation in mouse tongue epithelium was determined during unconventional fractionation schedules, i.e., hyperfractionation (2 x 1.5 and 2 x 1.75 Gy/day) and accelerated treatment (2 x 3 Gy/day). The residual tolerance of the epithelium at defined days of the fractionated treatment was tested by graded single test doses (top-up design). The dose required to induce complete epithelial denudation in 50% of the animals (ED50) was used to calculate the number of fractions repopulated during the preceding treatment. After the first week of hyperfractionation, tolerance was reduced compared to untreated epithelium. However, subsequently no further change was observed, indicating complete compensation of the weekly dose with all doses per fraction used. Epithelial cell density, defined by histological examination in additional experiments, in all fractionation arms decreased similarly by approximately 40% during the first week and remained constant at 60-80% in the subsequent 2 weeks. During accelerated fractionation, the residual mucosal tolerance decreased continuously with treatment time and resulted in epithelial denudation after 12 fractions. However, a substantial repopulation effect was observed, compensating 1.5 fractions by day 2, and 5 fractions by day 5, respectively. After cessation of the therapy the repopulation rate clearly decelerated to compensate a dose equivalent to about 0.5 fractions per day. Cell density decreased linearly during the treatment with 5, 10 or 12 fractions at a rate close to normal cell loss. Marked cell production, dependent on the total fractionated dose, was seen from one day after the last fraction in each experimental arm. These results indicate that maximum stem cell repopulation occurs predominantly during treatment, while major production of differentiating cells take place in treatment splits.

摘要

在非常规分割方案(即超分割,每天2次,每次1.5 Gy和1.75 Gy;以及加速治疗,每天2次,每次3 Gy)期间,对小鼠舌上皮的再增殖情况进行了测定。通过分级单次测试剂量(补充设计)来检测在分割治疗的特定天数时上皮的残余耐受性。用在50%的动物中诱导完全上皮剥脱所需的剂量(ED50)来计算在前一治疗期间再增殖的分割次数。超分割治疗第一周后,与未治疗的上皮相比,耐受性降低。然而,随后未观察到进一步变化,表明每周剂量与所用的每次分割剂量完全补偿。在额外实验中通过组织学检查确定的上皮细胞密度,在所有分割组中,第一周均类似地下降约40%,并在随后2周保持在60 - 80%不变。在加速分割期间,残余黏膜耐受性随治疗时间持续下降,12次分割后导致上皮剥脱。然而,观察到显著的再增殖效应,分别在第2天补偿1.5次分割,第5天补偿5次分割。治疗停止后,再增殖率明显减慢,以补偿相当于每天约0.5次分割的剂量。在进行5次、10次或12次分割治疗期间,细胞密度以接近正常细胞丢失的速率呈线性下降。在每个实验组最后一次分割后一天,可见明显的细胞生成,其依赖于总分割剂量。这些结果表明,最大程度的干细胞再增殖主要发生在治疗期间,而分化细胞的主要生成发生在治疗间隙。

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