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苯并[a]芘二醇环氧化物-DNA加合物的同步荧光分光光度法:一种检测因接触苯并[a]芘而导致的体外和体内DNA损伤的工具。

Synchronous fluorescence spectrophotometry of benzo[a]pyrene diol epoxide-DNA adducts: a tool for detection of in-vitro and in-vivo DNA damage by exposure to benzo[a]pyrene.

作者信息

Vähäkangas K, Pelkonen O, Harris C C

机构信息

Department of Pharmacology, University of Oulu, Finland.

出版信息

IARC Sci Publ. 1988(89):208-12.

PMID:3143671
Abstract

We have applied synchronous fluorescence spectrophotometry (SFS) to study benzo[a]pyrene diol epoxide (BPDE)-DNA adducts in biological samples. Adducts are measured as benzo[a]pyrene (BP) tetrols after acid hydrolysis, and give a peak at 374 nm of emission with a 34-nm wavelength difference. In vitro and in animal studies, there is a positive correlation between the amount of adducts and the BP dose. In cell culture studies, the amount of adducts is increased by increasing both the dose of BP and the time of culture with BP. In preliminary human studies, BPDE-DNA has been found by SFS in placental DNA from some but not all smoking mothers and in blood cell DNA from some individuals in occupationally exposed groups.

摘要

我们已应用同步荧光分光光度法(SFS)来研究生物样品中的苯并[a]芘二醇环氧化物(BPDE)-DNA加合物。加合物在酸水解后作为苯并[a]芘(BP)四醇进行测量,并在发射波长为374nm、波长差为34nm处出现一个峰值。在体外和动物研究中,加合物的量与BP剂量之间存在正相关。在细胞培养研究中,增加BP剂量和与BP一起培养的时间都会使加合物的量增加。在初步的人体研究中,通过SFS在部分但并非全部吸烟母亲的胎盘DNA以及职业暴露组中部分个体的血细胞DNA中发现了BPDE-DNA。

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