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重离子对兔组织的影响:高剂量辐射诱导视网膜光感受器细胞中的DNA链断裂

Effects of heavy ions on rabbit tissues: induction of DNA strand breaks in retinal photoreceptor cells by high doses of radiation.

作者信息

Lett J T, Keng P C, Bergtold D S, Howard J

出版信息

Radiat Environ Biophys. 1987;26(1):23-36. doi: 10.1007/BF01211362.

Abstract

Excised retinas from New Zealand white (NZW) rabbits were irradiated at 0 degrees C with 9-260 Gy (depending on the type of radiation) of 300 kVp X-rays, or the first 5 cm (range: approximately 14 cm in water) of 365 MeV/u Ne ions or 530 MeV/u Ar ions (LET infinity's: approximately 1, 35 +/- 3 and 90 +/- 5 keV/micron, respectively). Other positions (LET infinity's) in the Ne-ion beam (Bragg curve) were employed in more limited experiments. The retinas were frozen and stored in liquid nitrogen until analysis. Total strand breakage in the DNA of retinal photoreceptor (sensory) cells was determined from sedimentation profiles obtained by velocity sedimentation through reoriented alkaline sucrose gradients under conditions free from anomalies related to rotor speed. For the radiation doses employed: the reciprocal of the number average molecular weight, Mn, was related linearly to dose for each radiation quality and extrapolation to zero dose in each case gave positive intercepts for which the mean unirradiated molecular weight, M0, was 6.1 +/- 1.0 X 10(8) daltons; the efficiencies of total strand breakage for the different radiations were 50 +/- 3, 110 +/- 2 and 240 +/- 6 eV/strand break, respectively. For the heavy ions, accurate analogous calculations for other positions in the Bragg curves were precluded by beam degeneration due to fragmentation of the primary particles, etc. Overall, the experimental results support the concept that ionizing radiations damage cellular DNA by two general processes. One process causes localized damage, which under our experimental conditions is revealed as strand breaks and/or alkali-labile bonds in regions between molecules of size circa 10(9) daltons (subunits); the other causes essentially random damage. Base damage caused by either process would not have been delineated in our experiments.

摘要

将来自新西兰白兔(NZW)的切除视网膜在0摄氏度下用300 kVp的X射线9 - 260 Gy(取决于辐射类型),或365 MeV/u的氖离子或530 MeV/u的氩离子(无限线性能量转移分别约为1、35±3和90±5 keV/微米)照射前5厘米(在水中范围:约14厘米)。在更有限的实验中采用了氖离子束(布拉格曲线)中的其他位置(无限线性能量转移)。视网膜被冷冻并储存在液氮中直至分析。视网膜光感受器(感觉)细胞DNA中的总链断裂是根据在无与转子速度相关异常的条件下,通过重新定向的碱性蔗糖梯度进行速度沉降获得的沉降谱来确定的。对于所采用的辐射剂量:数均分子量Mn的倒数与每种辐射质量的剂量呈线性关系,并且在每种情况下外推至零剂量都得到正截距,其平均未照射分子量M0为6.1±1.0×10⁸道尔顿;不同辐射的总链断裂效率分别为50±(3)、110±2和240±6 eV/链断裂。对于重离子,由于初级粒子的碎片化等导致束流退化,使得无法对布拉格曲线中的其他位置进行准确的类似计算。总体而言,实验结果支持这样的概念,即电离辐射通过两个一般过程损伤细胞DNA。一个过程导致局部损伤,在我们的实验条件下表现为大小约为10⁹道尔顿(亚基)的分子之间区域的链断裂和/或碱不稳定键;另一个过程导致基本随机的损伤。在我们的实验中,任何一个过程引起的碱基损伤都不会被描绘出来。

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