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在体外接触拟除虫菊酯类产品会破坏小鼠着床前胚胎的发育。

In vitro exposure to pyrethroid-based products disrupts development of mouse preimplantation embryos.

机构信息

Institute of Animal Physiology, Centre of Biosciences, Slovak Academy of Sciences, Šoltésovej 4-6, 040 01 Košice, Slovak Republic.

Institute of Animal Physiology, Centre of Biosciences, Slovak Academy of Sciences, Šoltésovej 4-6, 040 01 Košice, Slovak Republic.

出版信息

Toxicol In Vitro. 2019 Jun;57:184-193. doi: 10.1016/j.tiv.2019.03.009. Epub 2019 Mar 7.

Abstract

The objective of this study was to evaluate the potential toxicity of pyrethroids (deltamethrin, permethrin, fenvalerate, λ-cyhalothrin), commercial pyrethroid-based products DECIS EW 50 (deltamethrin mixture), TOP SPOT ON STRONGER (permethrin mixture), as well as related secondary ingredients on mouse preimplantation embryo development. Two-cell stage embryos were in vitro cultured with addition of the listed chemicals until blastocyst formation. All active pyrethroids negatively affected embryonic development at 1000 μM concentration. Decreased quality of obtained blastocysts in permethrin, fenvalerate and λ-cyhalothrin-treated embryos was revealed as well. Deltamethrin showed harmful impact on embryo development at 100 μM concentration. Lower concentrations of pyrethroids (1, 10 μM) had no effect on embryo development. The presence of DECIS EW 50 containing deltamethrin at 100 μM caused degeneration of all embryos. Similarly, TOP SPOT ON STRONGER containing 100 μM of permethrin impaired embryonic development and quality of obtained blastocysts. Evaluated secondary ingredients (butylhydroxyanisol, butylhydroxytoluen, butylparaben and cyclohexanone) at corresponding concentrations showed damaging impact on preimplantation embryo development as well. Our results indicate that the embryotoxic potential of active pyrethroids is relatively low, whereas pyrethroid-based products have relatively high potential to impair mouse preimplantation development. Embryotoxicity of commercial products is probably attributable to the presence of secondary ingredients.

摘要

本研究旨在评估拟除虫菊酯(溴氰菊酯、氯菊酯、氰戊菊酯、高效氯氟氰菊酯)、商品化拟除虫菊酯产品 DECIS EW 50(溴氰菊酯混合物)、TOP SPOT ON STRONGER(氯菊酯混合物)以及相关次要成分对小鼠着床前胚胎发育的潜在毒性。将两细胞期胚胎进行体外培养,添加上述化学物质直至囊胚形成。所有活性拟除虫菊酯在 1000µM 浓度下均对胚胎发育产生负面影响。在经氯菊酯、氰戊菊酯和高效氯氟氰菊酯处理的胚胎中,获得的囊胚质量下降。溴氰菊酯在 100µM 浓度下对胚胎发育具有有害影响。较低浓度的拟除虫菊酯(1、10µM)对胚胎发育没有影响。含有 100µM 溴氰菊酯的 DECIS EW 50 的存在导致所有胚胎退化。同样,含有 100µM 氯菊酯的 TOP SPOT ON STRONGER 也损害了胚胎发育和获得的囊胚质量。评估的次要成分(丁基羟基茴香醚、丁基羟基甲苯、丁基对羟基苯甲酸酯和环己酮)在相应浓度下也对着床前胚胎发育产生了损害作用。我们的结果表明,活性拟除虫菊酯的胚胎毒性潜力相对较低,而基于拟除虫菊酯的产品具有较高的损害小鼠着床前发育的潜力。商业产品的胚胎毒性可能归因于次要成分的存在。

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