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2-[(氨丙基)氨基]乙硫醇对裂变中子诱导的DNA损伤和修复的影响。

The effect of 2-[(aminopropyl)amino] ethanethiol on fission-neutron-induced DNA damage and repair.

作者信息

Grdina D J, Sigdestad C P, Dale P J, Perrin J M

机构信息

Biological, Environmental and Medical Research Division, Argonne National Laboratory, IL 60439-4833.

出版信息

Br J Cancer. 1989 Jan;59(1):17-21. doi: 10.1038/bjc.1989.5.

Abstract

The effect(s) of the radioprotector 2-[(aminopropyl)amino] ethanethiol (WR 1065) on fission-neutron-induced DNA damage and repair in V79 Chinese hamster cells was determined by using a neutral filter elution procedure (pH 7.2). When required, WR1065, at a final working concentration of 4 mM, was added to the culture medium, either 30 min before and during irradiation with fission spectrum neutrons (beam energy of 0.85 MeV) from the JANUS research reactor, or for selected intervals of time following exposure. The frequency of neutron-induced DNA strand breaks as measured by neutral elution as a function of dose equalled that observed for 60Co gamma-ray-induced damage (relative biological effectiveness of one). In contrast to the protective effect exhibited by WR1065 in reducing 60Co-induced DNA damage, WR1065 was ineffective in reducing or protecting against induction of DNA strand breaks by JANUS neutrons. The kinetics of DNA double-strand rejoining were measured following neutron irradiation. In the absence of WR1065, considerable DNA degradation by cellular enzymes was observed. This process was inhibited when WR1065 was present. These results indicate that, under the conditions used, the quality (i.e. nature), rather than quantity, of DNA lesions (measured by neutral elution) formed by neutrons was significantly different from that formed by gamma-rays.

摘要

采用中性滤膜洗脱法(pH 7.2)测定了辐射防护剂2-[(氨丙基)氨基]乙硫醇(WR 1065)对V79中国仓鼠细胞中裂变中子诱导的DNA损伤及修复的影响。如有需要,将终浓度为4 mM的WR1065添加到培养基中,要么在使用JANUS研究堆的裂变谱中子(束流能量为0.85 MeV)进行辐照前30分钟及辐照期间添加,要么在辐照后选定的时间段添加。通过中性洗脱法测得的中子诱导的DNA链断裂频率与剂量的关系,与60Coγ射线诱导的损伤情况相同(相对生物效应为1)。与WR1065对减少60Co诱导的DNA损伤所表现出的保护作用相反,WR1065对减少或防止JANUS中子诱导的DNA链断裂无效。在中子辐照后测量了DNA双链重连的动力学。在没有WR1065的情况下,观察到细胞酶导致大量DNA降解。当存在WR1065时,这一过程受到抑制。这些结果表明,在所使用的条件下,中子诱导形成的DNA损伤(通过中性洗脱法测定)的性质而非数量,与γ射线诱导形成的损伤有显著差异。

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