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首页> 外文期刊>Hereditas >Genotoxic effects of ethyl methanesulfonate and X‐rays at different stages of rat spermatogenesis, studied by inhibition of DNA synthesis and induction of DNA repair in vitro
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Genotoxic effects of ethyl methanesulfonate and X‐rays at different stages of rat spermatogenesis, studied by inhibition of DNA synthesis and induction of DNA repair in vitro

机译:通过抑制DNA合成并诱导体外DNA修复研究了甲磺酸乙酯和X射线在大鼠精子形成不同阶段的遗传毒性作用

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摘要

Novel in vitro techniques have been developed for evaluation of genetic effects in rat spermatogenesis. The effects of chemical and physical model mutagens, ethyl methanesulfonate (EMS) and X-rays, on DNA synthesis have been compared at different stages of the seminiferous epithelial cycle. Inhibition of DNA synthesis, measured by (3H)-thymidine (3HTdR) and (125I)-iododeoxyuridine (125IUdR) incorporation assays, was observed in all stages in a dose dependent manner after EMS administration, whereas X-rays had only a slight inhibiting action. Unscheduled DNA synthesis (UDS) was analyzed by autoradiography of spermatogenic cell squashes. EMS induced UDS in all cell types except the most mature spermatids (steps 13–19). Highest induction was found in mid- and late pachytene primary spermatocytes at stages VII-XII, and a variable response in haploid cells. Step-12 spermatids were particularly sensitive, showing high induction of UDS. X-irradiation mainly affected mid- and late pachytene spermatocytes, but spermatids were only slightly affected.During meiosis and spermiogenesis, DNA is most susceptible to mutagen insult during maximal transcriptional activity at late steps of meiotic prophase. In addition, nuclear condensation phase at steps 9–12 of spermiogenesis is sensitive, which suggests a capacity of the germ cells to repair their genetic damage before the final inactivation of their chromatin.
机译:已经开发了新的体外技术来评估大鼠精子发生中的遗传效应。化学和物理模型诱变剂,甲磺酸乙酯(EMS)和X射线,在生精上皮循环的不同阶段比较了对DNA合成的影响。在EMS给药后,在各个阶段均以剂量依赖性的方式观察到通过(3H)-胸苷(3HTdR)和(125I)-碘脱氧尿苷(125IUdR)掺入法测定的DNA合成抑制作用,而X射线仅具有轻微的抑制作用行动。通过放射自显影生精细胞南瓜分析计划外的DNA合成(UDS)。 EMS可以诱导除最成熟的精子细胞之外的所有细胞类型的UDS(步骤13-19)。在VII-XII期的中期和后期的粗线初生精母细胞中发现了最高的诱导作用,并且在单倍体细胞中有不同的反应。第12步精子特别敏感,显示出对UDS的高度诱导。 X射线辐射主要影响中晚期的粗线期精母细胞,但精子只受到轻微影响。在减数分裂和生精过程中,DNA在减数分裂前期后期的最大转录活性期间最易受到诱变剂的侵害。此外,精子发生步骤9-12的核浓缩阶段很敏感,这表明生殖细胞有能力在染色质最终失活之前修复其遗传损伤。

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