Kreja L, Selig C, Nothdurft W
Institute for Occupational and Social Medicine, University of Ulm, Germany.
Mutat Res. 1996 Jan 16;359(1):63-70. doi: 10.1016/s0165-1161(96)90010-2.
DNA damage in single peripheral blood (pb) and bone marrow (bm) cells was studied in dogs which were exposed to total body X-ray irradiation (TBI) with a lethal dose of 3.9 Gy. The changes in pb and bm cell numbers were measured within 9 days after TBI. Using the alkaline single-cell gel electrophoresis technique ('comet' assay), DNA strand breaks and alkali labile sites were assessed in single cells derived from the blood before TBI, 1 h and 4 h after TBI and on days 1, 3 and 9 after TBI. Bone marrow cells subjected to the assay were collected before and on days 1 and 9 after TBI. Cells expressing the strongest DNA damage were most frequent in the blood 1 h after TBI and in the bone marrow 1 day after exposure. Thereafter, a continuous reduction of DNA damage in individual cells was observed in the course of progressive leukopenia and granulocytopenia.
对接受3.9 Gy致死剂量全身X射线照射(TBI)的犬只,研究了单个外周血(pb)和骨髓(bm)细胞中的DNA损伤。在TBI后9天内测量pb和bm细胞数量的变化。使用碱性单细胞凝胶电泳技术(“彗星”试验),在TBI前、TBI后1小时和4小时以及TBI后第1、3和9天,对血液来源的单个细胞中的DNA链断裂和碱不稳定位点进行评估。进行该试验的骨髓细胞在TBI前以及TBI后第1天和第9天收集。TBI后1小时血液中以及暴露后1天骨髓中表达最强DNA损伤的细胞最为常见。此后,在进行性白细胞减少和粒细胞减少过程中,观察到单个细胞中DNA损伤持续减少。