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建立造血急性辐射综合征和急性辐射暴露延迟效应的儿科小鼠模型。

Establishing Pediatric Mouse Models of the Hematopoietic Acute Radiation Syndrome and the Delayed Effects of Acute Radiation Exposure.

机构信息

Department of a Medicine, Indiana University School of Medicine, Indianapolis, Indiana.

Department of Biostatistics, Indiana University School of Medicine, Indianapolis, Indiana.

出版信息

Radiat Res. 2021 Apr 1;195(4):307-323. doi: 10.1667/RADE-20-00259.1.

Abstract

Medical countermeasures (MCMs) for hematopoietic acute radiation syndrome (H-ARS) should be evaluated in well-characterized animal models, with consideration of at-risk populations such as pediatrics. We have developed pediatric mouse models of H-ARS and delayed effects of acute radiation exposure (DEARE) for efficacy testing of MCMs against radiation. Male and female C57BL/6J mice aged 3, 4, 5, 6, 7 and 8 weeks old (±1 day) were characterized for baseline hematopoietic and gastrointestinal parameters, radiation response, efficacy of a known MCM, and DEARE at six and 12 months after total-body irradiation (TBI). Weanlings (age 3 weeks) were the most radiosensitive age group with an estimated LD50/30 of 712 cGy, while mice aged 4 to 8 weeks were more radioresistant with an estimated LD50/30 of 767-787 cGy. Female weanlings were more radiosensitive than males at 3 and 4 weeks old but became significantly more radioresistant after the pubertal age of 5 weeks. The most dramatic increase in body weight, RBC counts and intestinal circumference length occurred from 3 to 5 weeks of age. The established radiomitigator Neulasta® (pegfilgrastim) significantly increased 30-day survival in all age groups, validating these models for MCM efficacy testing. Analyses of DEARE among pediatric survivors revealed depressed weight gain in males six months post-TBI, and increased blood urea nitrogen at 12 months post-TBI which was more severe in females. Hematopoietic DEARE at six months post-TBI appeared to be less severe in survivors from the 3- and 4-week-old groups but was equally severe in all age groups by 12 months of age. Similar to our other acute radiation mouse models, there was no appreciable effect of Neulasta used as an H-ARS MCM on the severity of DEARE. In summary, these data characterize a pediatric mouse model useful for assessing the efficacy of MCMs against ARS and DEARE in children.

摘要

造血急性辐射综合征 (H-ARS) 的医学对策 (MCM) 应在特征明确的动物模型中进行评估,并考虑儿科等高危人群。我们已经开发了小儿 H-ARS 和急性辐射暴露延迟效应 (DEARE) 的小鼠模型,用于针对辐射的 MCM 功效测试。3、4、5、6、7 和 8 周龄(±1 天)的雄性和雌性 C57BL/6J 小鼠用于基线造血和胃肠道参数、辐射反应、一种已知 MCM 的功效以及全身照射 (TBI) 后 6 个月和 12 个月的 DEARE 特征描述。3 周龄的幼鼠(年龄 3 周)是最敏感的年龄组,估计 LD50/30 为 712 cGy,而 4 至 8 周龄的小鼠则更具辐射抗性,估计 LD50/30 为 767-787 cGy。3 和 4 周龄时,雌性幼鼠比雄性幼鼠更敏感,但在 5 周龄的青春期后,雌性幼鼠的辐射抗性显著增强。体重、RBC 计数和肠围长度的最大增加发生在 3 至 5 周龄之间。既定的辐射缓解剂 Neulasta®(聚乙二醇化粒细胞集落刺激因子)显著提高了所有年龄组的 30 天存活率,验证了这些模型用于 MCM 功效测试。儿科幸存者的 DEARE 分析显示,TBI 后 6 个月雄性体重增加减少,TBI 后 12 个月血尿素氮增加,女性更为严重。6 个月时的造血 DEARE 在 3 至 4 周龄组的幸存者中似乎不那么严重,但在 12 个月时所有年龄组的严重程度相同。与我们的其他急性辐射小鼠模型一样,Neulasta 作为 H-ARS MCM 对 DEARE 严重程度没有明显影响。总之,这些数据描述了一种小儿小鼠模型,可用于评估针对儿童 ARS 和 DEARE 的 MCM 的功效。

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