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首页> 外文期刊>Mutagenesis >Radiation-induced DNA damage and the relative biological effectiveness of 18F-FDG in wild-type mice.
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Radiation-induced DNA damage and the relative biological effectiveness of 18F-FDG in wild-type mice.

机译:辐射诱导的DNA损伤和18F-FDG在野生型小鼠中的相对生物效果。

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摘要

Clinically, the most commonly used positron emission tomography (PET) radiotracer is the glucose analog 2-[(18)F] fluoro-2-deoxy-D-glucose ((18)F-FDG), however little research has been conducted on the biological effects of (18)F-FDG injections. The induction and repair of DNA damage and the relative biological effectiveness (RBE) of radiation from (18)F-FDG relative to 662 keV γ-rays were investigated. The study also assessed whether low-dose radiation exposure from (18)F-FDG was capable of inducing an adaptive response. DNA damage to the bone marrow erythroblast population was measured using micronucleus formation and lymphocyte γH2A.X levels. To test the RBE of (18)F-FDG, mice were injected with a range of activities of (18)F-FDG (0-14.80 MBq) or irradiated with Cs-137 γ-rays (0-100 mGy). The adaptive response was investigated 24h after the (18)F-FDG injection by 1 Gy in vivo challenge doses for micronucleated reticulocyte (MN-RET) formation or 1, 2 and 4 Gy in vitro challenges doses for γH2A.X formation. A significant increase in MN-RET formation above controls occurred following injection activities of 3.70, 7.40 or 14.80 MBq (P < 0.001) which correspond to bone marrow doses of ~35, 75 and 150 mGy, respectively. Per unit dose, the Cs-137 radiation exposure induced significantly more damage than the (18)F-FDG injections (RBE = 0.79 ± 0.04). A 20% reduction in γH2A.X fluorescence was observed in mice injected with a prior adapting low dose of 14.80 MBq (18)F-FDG relative to controls (P < 0.019). A 0.74 MBq (18)F-FDG injection, which gives mice a dose approximately equal to a typical human PET scan, did not cause a significant increase in DNA damage nor did it generate an adaptive response. Typical (18)F-FDG injection activities used in small animal imaging (14.80 MBq) resulted in a decrease in DNA damage, as measured by γH2A.X formation, below spontaneous levels observed in control mice. The (18)F-FDG RBE was <1.0, indicating that the mixed radiation quality and/or low dose rate from PET scans is less damaging than equivalent doses of gamma radiation.
机译:临床上,最常用的正电子发射断层扫描(PET)辐射酸酯是葡萄糖类似物2 - [(18)F]氟-2-脱氧-D-葡萄糖((18)F-FDG),但是对研究进行了很少的研究(18)F-FDG注射的生物学效应。研究了DNA损伤的诱导和修复和来自(18)F-FDG相对于662keVγ射线的辐射的相对生物效果(RBE)。该研究还评估了来自(18)F-FDG的低剂量辐射暴露是否能够诱导适应性反应。使用微核形成和淋巴细胞γH2a.x水平测量对骨髓红细胞群的DNA损伤。为了测试(18)F-FDG的RBE,用(18)F-FDG(0-14.80mbq)的一系列活性注射小鼠,或用CS-137γ射线(0-100 MGO)照射。在(18)F-FDG注射后,在体内挑战剂量(Mn-RET)形成或1,2和4 Gy的体外挑战剂量中,对(18)F-FDG注射剂进行了1Gy,在γH2a.x的体外挑战剂量的体外攻击剂量中进行了γ攻击剂量的1Gy,进行了治疗响应。在注射活性的3.70,70或14.80 MBQ(P <0.001)的注射活性后,对对照的对照进行显着增加,该骨髓剂量分别对应于〜35,75和150 MGY的骨髓剂量。每单位剂量,CS-137辐射暴露诱导损伤明显多于(18)F-FDG注射(RBE = 0.79±0.04)。在注射的小鼠中观察到γH2A.x荧光的20%降低,所述小鼠相对于对照(P <0.019)。 0.74 MBQ(18)F-FDG注射液,其给小鼠的剂量大约等于典型的人PET扫描,没有导致DNA损伤的显着增加也没有产生适应性响应。小动物成像中使用的典型(18)F-FDG注射活性导致DNA损伤的降低,通过γH2A.x形成,低于对照小鼠观察到的自发水平。 (18)F-FDG RBE为<1.0,表明来自PET扫描的混合辐射质量和/或低剂量率比当量的γ辐射的损伤较小。

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