Department of Radiobiology, Institut de Recherche Biomédicale des Armées, La Tronche, France.
Health Phys. 2012 Aug;103(2):143-9. doi: 10.1097/HP.0b013e3182475e54.
This biodosimetry study used irradiated baboons to investigate the efficacy of a kinetic multiparameter (clinical, physical, and biological) approach for discriminating partial-body irradiation (PBI) and total-body irradiation (TBI). Animals were unilaterally (front) exposed to 60Co gamma rays (8 to 32 cGy min) using either TBI or vertical left hemi-body irradiation (HBI), as follows: 2.5 Gy TBI (n = 2), 5 Gy TBI (n = 2), 5 Gy HBI (n = 2), and 10 Gy HBI (n = 2). Midline tissue doses were measured at the anterior iliac crest level with an ionization chamber, and body dosimetry was performed using thermoluminescent dosimeters. Blood samples were collected before exposure and from 1 h until 200 d after irradiation. Clinical status, complete blood cell count, biochemical parameters, and cytogenetic analysis were evaluated. The partial least square discriminant analysis chosen for statistical analysis showed that the four groups of irradiated baboons were clearly separated. However, the dicentric chromosome assay may not distinguish HBI from TBI in confounding situations where equivalent whole-body doses are similar and the time of exposure is sufficient for peripheral blood lymphocyte homogenization. Interestingly, as bone marrow shielding in HBI animals prevented aplasia from happening, hematologic parameters such as the platelet count and Flt-3 ligand level helped to distinguish HBI and TBI. Moreover, the ratio of neutrophil to lymphocyte counts, creatine kinase, and citrulline levels may be discriminating biomarkers of dose or injury. Both early and delayed clinical signs and bioindicators appear to be useful for assessment of heterogeneous irradiation.
本生物剂量学研究使用辐照狒狒来研究一种动力学多参数(临床、物理和生物学)方法对于区分全身局部照射(PBI)和全身照射(TBI)的效果。动物通过单侧(前)暴露于 60Coγ射线(8 至 32 cGy min)接受 TBI 或垂直左侧半身照射(HBI),如下所示:2.5 Gy TBI(n = 2)、5 Gy TBI(n = 2)、5 Gy HBI(n = 2)和 10 Gy HBI(n = 2)。使用电离室测量前髂嵴水平的中线组织剂量,并使用热释光剂量计进行体剂量测量。在照射前和照射后 1 小时至 200 天采集血液样本。评估临床状态、全血细胞计数、生化参数和细胞遗传学分析。选择用于统计分析的偏最小二乘判别分析表明,四组辐照狒狒明显分开。然而,当等效全身剂量相似且暴露时间足以使外周血淋巴细胞均匀化时,双着丝粒染色体试验可能无法区分 HBI 与 TBI。有趣的是,由于 HBI 动物的骨髓屏蔽防止了再生障碍的发生,血小板计数和 Flt-3 配体水平等血液学参数有助于区分 HBI 和 TBI。此外,中性粒细胞与淋巴细胞计数比、肌酸激酶和瓜氨酸水平可能是剂量或损伤的鉴别生物标志物。早期和晚期临床症状和生物标志物似乎都可用于评估不均匀照射。