利用缺口翻译试验测定暴露于环境烟草烟雾的吸烟者和非吸烟者淋巴细胞DNA单链断裂。

M Einhaus, O Holz, R Meissner, T Krause, K Warncke, I Held, G Scherer, A R Tricker, F Adlkofer, H W Rüdiger
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引用次数: 5

摘要

在人类单核白细胞(MWBC) DNA单链断裂(SSB)的检测使用改进版本的缺口翻译试验提出。该试验允许快速和敏感的检查SSB只使用5毫升肝素化血8倍测定。用已知基因毒性物质n -甲基-n′-硝基-n -亚硝基胍(MNNG)体外孵育MBWC,使该方法标准化。MWBC与MNNG的体外孵育诱导了5至500微米MNNG剂量下DNA-SSB的剂量依赖性增加。该方法的检出限为5 μ m - MNNG。为了评估该方法在体内检测SSB的适用性,我们进行了一项对照研究,将自愿吸烟者(n = 5)、暴露于环境烟草烟雾(ETS)的非吸烟者(n = 5)和非吸烟者对照(n = 5)进行比较。试验期4 d,对照组2 d,暴露期2 d。在对照日(第1天和第3天),吸烟者和不吸烟者在不通风的45立方米房间里坐8小时。在暴露日(第2天和第4天),5名吸烟者在8小时内每人吸24支烟,而5名不吸烟者暴露在吸烟志愿者产生的ETS中。通过碳氧血红蛋白(CO-Hb)、血浆尼古丁和可替宁水平的剂量测定证实了高暴露于烟草烟雾。在所有4天的实验中,每次暴露前后均抽血,在血细胞分离后立即测定淋巴细胞中的DNA-SSB。(摘要删节250字)
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Determination of DNA single-strand breaks in lymphocytes of smokers and nonsmokers exposed to environmental tobacco smoke using the nick translation assay.

The detection of DNA single-strand breaks (SSB) in human mononucleated white blood cells (MWBC) using a modified version of the nick translation assay is presented. This assay allows rapid and sensitive examination of SSB using only 5 ml heparinized blood for an eightfold determination. The assay was standardized by incubation of MBWC in vitro with N-methyl-N'-nitro-N-nitrosoguanidine (MNNG), a known genotoxic agent. In vitro incubation of MWBC with MNNG induced a dose-dependent increase in DNA-SSB at doses between 5 and 500 microM MNNG. The detection limit for the assay was 5 microM MNNG. To assess the suitability of this assay to detect SSB in vivo a controlled study was performed in which volunteer smokers (n = 5), nonsmokers (n = 5) exposed to environmental tobacco smoke (ETS), and nonsmokers controls (n = 5) were compared. The study lasted 4 experimental days, 2 control and 2 exposure days. On control days (days 1 and 3) smokers and nonsmokers sat in an unventilated 45 m3 room for 8 h. On the exposure days (days 2 and 4) each of the five smokers smoked 24 cigarettes in 8 h, while the five nonsmokers were exposed to the ETS generated by the smoking volunteers. High exposure to tobacco smoke was confirmed by dosimetry of carboxyhemoglobin (CO-Hb), plasma nicotine and cotinine levels. Blood was drawn before and after each exposure on all 4 experimental days for determination of DNA-SSB in lymphocytes immediately after isolation of blood cells.(ABSTRACT TRUNCATED AT 250 WORDS)

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