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利用斑马鱼胚胎毒性试验对石油物质进行产前发育毒性测试。

Prenatal developmental toxicity testing of petroleum substances using the zebrafish embryotoxicity test.

机构信息

Division of Toxicology, Wageningen University and Research, Wageningen, The Netherlands.

Animal Sciences Group, Cell Biology and Immunology, Wageningen University and Research, Wageningen, The Netherlands.

出版信息

ALTEX. 2019;36(2):245-260. doi: 10.14573/altex.1808121. Epub 2018 Dec 7.

Abstract

The present study evaluates the applicability of the zebrafish embryotoxicity test (ZET) to assess prenatal developmental toxicity (PDT) potency of the DMSO-extracts of 9 petroleum substances (PS), with variable polycyclic aromatic hydrocarbon (PAH) content, and 2 gas-to-liquid (GTL) products, without any PAHs but otherwise similar properties to PS. The results showed that all PS extracts induced concentration-dependent in vitro PDT, as quantified in the ZET and that this potency is associated with their 3-5 ring PAH content. In contrast and as expected, GTL products did not induce any effect at all. The potencies obtained in the ZET correlated with those previously reported for the embryonic stem cell test (EST) (R2=0.61), while the correlation with potencies reported in in vivo studies were higher for the EST (R2=0.85) than the ZET (R2=0.69). Combining the results of the ZET with those previously reported for the EST (Kamelia et al., 2017), the aryl hydrocarbon (AhR) CALUX assay (Kamelia et al., 2018), and the PAH content, ranked and clustered the test compounds in line with their in vivo potencies and chemical characteristics. To conclude, our findings indicate that the ZET does not outperform the EST as a stand-alone assay for testing PDT of PS, but confirms the hypothesis that PAHs are the major inducers of PDT by some PS, while they also indicate that the ZET is a useful addition to a battery of in vitro tests able to predict the in vivo PDT of PS.

摘要

本研究评估了斑马鱼胚胎毒性测试(ZET)在评估 9 种石油物质(PS)和 2 种气转液(GTL)产品的 DMSO 提取物的产前发育毒性(PDT)效力方面的适用性,这些 PS 提取物的多环芳烃(PAH)含量不同,而 GTL 产品则不含任何 PAH,但具有与 PS 相似的性质。结果表明,所有 PS 提取物均诱导了浓度依赖性的体外 PDT,这在 ZET 中得到了量化,并且这种效力与它们的 3-5 环 PAH 含量有关。相比之下,正如预期的那样,GTL 产品根本没有引起任何影响。在 ZET 中获得的效力与先前报道的胚胎干细胞测试(EST)中的效力相关(R2=0.61),而与体内研究中报道的效力的相关性在 EST 中更高(R2=0.85)比 ZET(R2=0.69)。将 ZET 的结果与先前报道的 EST(Kamelia 等人,2017)、芳烃(AhR)CALUX 测定(Kamelia 等人,2018)和 PAH 含量相结合,根据它们的体内效力和化学特征对测试化合物进行了排序和聚类。总之,我们的研究结果表明,ZET 作为一种独立的 PDT 测试方法并不优于 EST,但证实了这样一种假设,即某些 PS 中的 PAH 是 PDT 的主要诱导剂,同时也表明 ZET 是一系列体外测试的有用补充,这些测试能够预测 PS 的体内 PDT。

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