Travis E L, Peters L J, McNeill J, Thames H D, Karolis C
Radiother Oncol. 1985 Dec;4(4):341-51. doi: 10.1016/s0167-8140(85)80122-5.
The effect of low dose-rate total body irradation (TBI) on hemopoietic and nonhemopoietic lethality has been studied in BALB/c mice using dose-rates ranging from 25 to 1 cGy/min. Deaths were scored at 10 days, 30 days, and one year after irradiation, and dose-response curves were constructed to determine the dose-rate dependence of deaths from the gastrointestinal syndrome, hemopoietic syndrome, and late lethal syndrome(s), respectively. A plot of the LD50S for each of these lethal syndromes versus dose-rate showed the dose-rate dependence for late lethality to be somewhat greater than that for gut death, but both of these endpoints were markedly more dose-rate dependent than was hemopoietic lethality, particularly at dose rates less than 5 cGy/min. To determine which late responding normal tissues might be critical for low dose-rate TBI, complete necropsies were performed on all mice dying later than 60 days after irradiation and on all mice surviving at one year; all tissues were examined histologically. Morphologic evidence of radiation injury was present in only three tissues, lung (fibrosis and scarring) kidney (tubule depletion), and liver (presence of mitoses). Subjectively, the lung changes were most severe up to 9 months while kidney changes became more prominent after this time, suggesting that late death after low dose-rate TBI may not be entirely attributable to lung injury. However, regardless of which late responding normal tissue is dose-limiting, it is clear that low dose-rate TBI preferentially spares these tissues compared with hemopoietic stem cells.
利用25至1 cGy/分钟的剂量率,在BALB/c小鼠中研究了低剂量率全身照射(TBI)对造血和非造血致死率的影响。在照射后10天、30天和1年时记录死亡情况,并构建剂量反应曲线,以分别确定胃肠道综合征、造血综合征和晚期致死综合征导致死亡的剂量率依赖性。针对每种致死综合征的LD50与剂量率的关系图显示,晚期致死率的剂量率依赖性略高于肠道死亡,但这两个终点的剂量率依赖性均明显高于造血致死率,尤其是在剂量率低于5 cGy/分钟时。为了确定哪些晚期反应正常组织可能对低剂量率TBI至关重要,对所有在照射后60天以后死亡的小鼠以及所有存活1年的小鼠进行了完整的尸检;对所有组织进行了组织学检查。仅在三个组织中发现了辐射损伤的形态学证据,即肺(纤维化和瘢痕形成)、肾(肾小管缺失)和肝(有丝分裂存在)。主观上,肺的变化在9个月内最为严重,而此后肾的变化变得更加明显,这表明低剂量率TBI后的晚期死亡可能并非完全归因于肺损伤。然而,无论哪个晚期反应正常组织是剂量限制因素,显然与造血干细胞相比,低剂量率TBI能优先保护这些组织。