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用碱性解旋技术测定甲磺酸甲酯和二甲基亚砜诱导的小鼠各器官DNA中的单链断裂。

Single-strand breaks in DNA of various organs of mice induced by methyl methanesulfonate and dimethylsulfoxide determined by the alkaline unwinding technique.

作者信息

Solveig Walles S A, Erixon K

出版信息

Carcinogenesis. 1984 Mar;5(3):319-23. doi: 10.1093/carcin/5.3.319.

Abstract

The method for determination of single-strand breaks (SSB) in DNA by the technique of alkaline unwinding and hydroxylapatite chromatography has been applied for cell nuclei from organs of mice. Male mice were given methyl methane-sulfonate (MMS) and dimethylsulfoxide (DMSO) by i.p. administration. Cell nuclei were prepared from various organs and then lysed in alkali. The amount of DNA was determined by fluorometry using 4',6-diamidino-2-phenylindole.2HCl. The relative level of SSB in DNA was determined in various organs (liver, kidney, lung, spleen, testis and brain) 1-24 h after administration of the agent. After MMS-treatment the number of SSB in DNA increased to about the same extent in all organs 1 h post-treatment but then decreased by time. The SSB persisted for the longest time in brain- and lung-DNA. DMSO induced SSB only in DNA of kidney.

摘要

通过碱性解旋和羟基磷灰石色谱技术测定DNA中单链断裂(SSB)的方法已应用于小鼠器官的细胞核。雄性小鼠经腹腔注射甲基磺酸甲酯(MMS)和二甲基亚砜(DMSO)。从各种器官制备细胞核,然后在碱中裂解。使用4',6-二脒基-2-苯基吲哚二盐酸盐通过荧光法测定DNA的量。在给予药剂后1至24小时,在各种器官(肝脏、肾脏、肺、脾脏、睾丸和大脑)中测定DNA中SSB的相对水平。MMS处理后,处理后1小时所有器官中DNA的SSB数量增加到大致相同的程度,但随后随时间减少。SSB在脑和肺DNA中持续时间最长。DMSO仅在肾脏DNA中诱导产生SSB。

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