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In vitro evaluation of baseline and induced DNA damage in human sperm exposed to benzoapyrene or its metabolite benzoapyrene-78-diol-910-epoxide using the comet assay

机译:使用彗星试验体外评估暴露于苯并a py或其代谢产物苯并a py-78-二醇-910-环氧化合物的人类精子的基线和诱导的DNA损伤

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摘要

Exposure to genotoxins may compromise DNA integrity in male reproductive cells, putting future progeny at risk for developmental defects and diseases. To study the usefulness of sperm DNA damage as a biomarker for genotoxic exposure, we have investigated cellular and molecular changes induced by benzo[a]pyrene (B[a]P) in human sperm in vitro, and results have been compared for smokers and non-smokers. Sperm DNA obtained from five smokers was indeed more fragmented than sperm of six non-smokers (mean % Tail DNA 26.5 and 48.8, respectively), as assessed by the alkaline comet assay (P < 0.05). B[a]P-related DNA adducts were detected at increased levels in smokers as determined by immunostaining. Direct exposure of mature sperm cells to B[a]P (10 or 25 μM) caused moderate increases in DNA fragmentation which was independent of addition of human liver S9 mix for enzymatic activation of B[a]P, suggesting some unknown metabolism of B[a]P in ejaculates. In vitro exposure of samples to various doses of B[a]P (with or without S9) did not reveal any significant differences in sensitivity to DNA fragmentation between smokers and non-smokers. Incubations with the proximate metabolite benzo[a]pyrene-r-7,t-8-dihydrodiol-t9,10-epoxide (BPDE) produced DNA fragmentation in a dose-dependent manner (20 or 50 μM), but only when formamidopyrimidine DNA glycosylase treatment was included in the comet assay. These levels of DNA fragmentation were, however, low in relation to very high amounts of BPDE–DNA adducts as measured with 32P postlabelling. We conclude that sperm DNA damage may be useful as a biomarker of direct exposure of sperm using the comet assay adapted to sperm, and as such the method may be applicable to cohort studies. Although the sensitivity is relatively low, DNA damage induced in earlier stages of spermatogenesis may be detected with higher efficiencies.
机译:暴露于基因毒素可能会损害男性生殖细胞中的DNA完整性,使未来的后代处于发育缺陷和疾病的风险中。为了研究精子DNA损伤作为遗传毒性暴露生物标志物的有用性,我们研究了苯并[a] re(B [a] P)在人精子中诱导的细胞和分子变化,并在吸烟者和吸烟者之间进行了比较。不吸烟者。通过碱性彗星试验(P <0.05),从五名吸烟者获得的精子DNA确实比六名不吸烟者的精子更碎(分别为尾巴DNA的平均百分比26.5和48.8)。通过免疫染色测定,在吸烟者中检测到B [a] P相关的DNA加合物水平升高。成熟精细胞直接暴露于B [a] P(10或25μM)会引起DNA片段的适度增加,这与添加人肝S9混合物以酶促B [a] P无关,这表明B的某些未知代谢[a] P射精。样品在体外暴露于各种剂量的B [a] P(有或没有S9)下,吸烟者和非吸烟者对DNA片段敏感性的差异均无显着性差异。与最近的代谢产物苯并[a] py-r-7,t-8-二氢二醇-t9,10-环氧化物(BPDE)一起温育会产生剂量依赖性(20或50μM)的DNA片段化,但仅在甲酰胺嘧啶DNA时彗星试验中包括糖基化酶处理。然而,与 32 P后标记法测得的BPDE-DNA加合物数量相比,这些DNA片段化水平较低。我们得出的结论是,使用适应于精子的彗星试验,精子DNA损伤可用作直接暴露精子的生物标记,因此该方法可能适用于队列研究。尽管敏感性相对较低,但是可以以更高的效率检测在精子发生早期阶段诱导的DNA损伤。

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