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[建立用于评估发育神经毒性的胚胎干细胞并测试胚胎干细胞的验证]

[Establishment of embryonic stem cell for evaluation of development neurotoxicity and test the validation of embryonic stem cell].

作者信息

Yu Zhou, Xu Haibin

机构信息

Institute of Nutrition and Food Safety, China CDC, Beijing 100021, China.

出版信息

Wei Sheng Yan Jiu. 2010 Nov;39(6):685-8.

Abstract

OBJECTIVE

To establish embryonic stem cell (EST) for evaluation of developmental neurontoxicity and test the validation of EST.

METHODS

RT-PCR method was used to study the influence of fluorouracil (5-FU), diphenylhydantoin (DPH) and Penicillin G at the different concentrations on neuron cells with nestin expression that differentiate from embryonic stem cells (ES). With the results of cells viability (ES and BALB/c) assessed by MTT, the developmental neurotoxicty characteristics of 5-FU, DPH and Penicillin G may be identified clearly. RESULTS; The ID50 D3 nestin concentration of three embryotoxicants were 0.017, 49.4 and 1139 microg/ml. Penicillin G, DPH and 5-FU were discriminated as none-, weak- and strong- developmental neurotoxicity. CONCLUSION; Test compounds among three classes were discriminated correctly. The EST on developmental neurontoxicity could be applied to the safety evaluation in vitro.

摘要

目的

建立用于评估发育性神经毒性的胚胎干细胞(EST)并测试其有效性。

方法

采用逆转录聚合酶链反应(RT-PCR)方法,研究不同浓度的氟尿嘧啶(5-FU)、苯妥英(DPH)和青霉素G对从胚胎干细胞(ES)分化而来的表达巢蛋白的神经细胞的影响。通过MTT法评估细胞活力(ES和BALB/c)结果,可明确5-FU、DPH和青霉素G的发育神经毒性特征。结果:三种胚胎毒性物质的ID50 D3巢蛋白浓度分别为0.017、49.4和1139微克/毫升。青霉素G、DPH和5-FU分别被判定为无、弱和强发育神经毒性。结论:三类受试化合物被正确区分。发育性神经毒性的EST可用于体外安全性评估。

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