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Assessment of 1,2-propanediol (PrOH) genotoxicity on mouse oocytes by comet assay.

机译:通过彗星试验评估1,2-丙二醇(PrOH)对小鼠卵母细胞的遗传毒性。

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OBJECTIVE: To assess the genotoxicity of 1,2-propanediol (PrOH) on mouse oocytes by comet assay. DESIGN: In vitro assay using murine model. SETTING: Biogenotoxicology research laboratory. ANIMAL(S): CD1 female mice. INTERVENTION(S): Three 40-oocyte groups were exposed to different PrOH concentrations (5%, 7.5%, and 15%). Each concentration was tested during both long and short exposures (1-2 hours and 1-5 minutes) in comparison with control groups. DNA damage was evaluated by a single-cell gel electrophoresis assay, also called "comet assay," and analyzed with Komet software. MAIN OUTCOME MEASURE(S): DNA damage was quantified as Olive tail moment (OTM). Interpretation was done on OTM with the use of chi(2). RESULT(S): High PrOH concentrations (7.5% and 15%) induced significant DNA damage on mouse oocytes. The OTM chi(2) values were 4.16 +/- 0.40 and 6.80 +/- 0.4 with 7.5% PrOH at 1 and 2 hours, respectively, 24.35 +/- 1.60 with 15% at 1 hour, and for 2h at 15% the DNA damage was too drastic to calculate OTM chi(2). After 1 and 5 minutes, the OTM chi(2) values were, respectively, 5.19 +/- 0.26 and 6.06 +/- 0.42 with 7.5%, and 7.53 +/- 0.33 and 16.81 +/- 0.67 with 15%. CONCLUSION(S): High concentrations of PrOH (7.5% and 15%) induced significant DNA damage on mouse oocytes, whatever the exposure duration. These results should be interpreted with caution, because additional data are needed to evaluate PrOH genotoxicity and DNA oocyte reparation after exposure to high PrOH concentrations.
机译:目的:通过彗星试验评估1,2-丙二醇(PrOH)对小鼠卵母细胞的遗传毒性。设计:使用鼠模型进行体外测定。单位:生物遗传毒理学研究实验室。动物:CD1雌性小鼠。干预:三个40卵母细胞组暴露于不同的PrOH浓度(5%,7.5%和15%)。与对照组相比,在长时间和短期暴露(1-2小时和1-5分钟)中都测试了每种浓度。通过单细胞凝胶电泳测定法(也称为“彗星测定法”)评估DNA损伤,并使用Komet软件进行分析。主要观察指标:DNA损伤定量为橄榄尾矩(OTM)。使用chi(2)在OTM上进行解释。结果:高PrOH浓度(7.5%和15%)对小鼠卵母细胞产生明显的DNA损伤。 OTM chi(2)值分别为1.16和2小时,含7.5%PrOH的4.16 +/- 0.40和6.80 +/- 0.4,1小时为15%的24.35 +/- 1.60和15%的2h。 DNA损伤太严重,无法计算OTM chi(2)。 1分钟和5分钟后,OTM chi(2)值分别为5.19 +/- 0.26和6.06 +/- 0.42(7.5%)和7.53 +/- 0.33和16.81 +/- 0.67(15%)。结论:无论暴露时间长短,高浓度的PrOH(分别为7.5%和15%)都会对小鼠卵母细胞造成明显的DNA损伤。应谨慎解释这些结果,因为在暴露于高浓度的PrOH后,还需要其他数据来评估PrOH的遗传毒性和DNA卵母细胞修复。

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