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本文引用的文献

1
Exposure-Based Validation of an In Vitro Gastrulation Model for Developmental Toxicity Assays.基于暴露的体外原肠胚形成模型用于发育毒性检测的验证。
Toxicol Sci. 2017 May 1;157(1):235-245. doi: 10.1093/toxsci/kfx034.
2
Adverse effect of valproic acid on an in vitro gastrulation model entails activation of retinoic acid signaling.丙戊酸对体外原肠胚形成模型的不良影响需要激活视黄酸信号通路。
Reprod Toxicol. 2016 Dec;66:68-83. doi: 10.1016/j.reprotox.2016.09.015. Epub 2016 Sep 29.
3
A hard look at FDA's review of GRAS notices.深入审视美国食品药品监督管理局对一般认为安全(GRAS)通知的审查。
Regul Toxicol Pharmacol. 2016 Aug;79 Suppl 2:S124-8. doi: 10.1016/j.yrtph.2016.06.011. Epub 2016 Jun 16.
4
A Modified Murine Embryonic Stem Cell Test for Evaluating the Teratogenic Effects of Drugs on Early Embryogenesis.一种用于评估药物对早期胚胎发育致畸作用的改良小鼠胚胎干细胞试验。
PLoS One. 2015 Dec 18;10(12):e0145286. doi: 10.1371/journal.pone.0145286. eCollection 2015.
5
An in vitro gastrulation model recapitulates the morphogenetic impact of pharmacological inhibitors of developmental signaling pathways.体外原肠胚形成模型再现了发育信号通路药理学抑制剂的形态发生影响。
Mol Reprod Dev. 2015 Dec;82(12):1015-36. doi: 10.1002/mrd.22585. Epub 2015 Oct 9.
6
Use of In Vitro Morphogenesis of Mouse Embryoid Bodies to Assess Developmental Toxicity of Therapeutic Drugs Contraindicated in Pregnancy.利用小鼠胚胎体的体外形态发生来评估孕期禁用治疗药物的发育毒性。
Toxicol Sci. 2016 Jan;149(1):15-30. doi: 10.1093/toxsci/kfv209. Epub 2015 Sep 18.
7
Paired Serum and Urine Concentrations of Biomarkers of Diethyl Phthalate, Methyl Paraben, and Triclosan in Rats.大鼠体内邻苯二甲酸二乙酯、对羟基苯甲酸甲酯和三氯生生物标志物的血清和尿液配对浓度
Environ Health Perspect. 2016 Jan;124(1):39-45. doi: 10.1289/ehp.1409586. Epub 2015 Jun 5.
8
Exposure-based validation list for developmental toxicity screening assays.
Birth Defects Res B Dev Reprod Toxicol. 2014 Dec;101(6):423-8. doi: 10.1002/bdrb.21132. Epub 2014 Dec 4.
9
Morphology-based mammalian stem cell tests reveal potential developmental toxicity of donepezil.基于形态学的哺乳动物干细胞测试揭示了多奈哌齐潜在的发育毒性。
Mol Reprod Dev. 2014 Nov;81(11):994-1008. doi: 10.1002/mrd.22423. Epub 2014 Sep 30.
10
Transcriptomic characterization of C57BL/6 mouse embryonic stem cell differentiation and its modulation by developmental toxicants.C57BL/6小鼠胚胎干细胞分化的转录组学特征及其受发育毒物的调控
PLoS One. 2014 Sep 23;9(9):e108510. doi: 10.1371/journal.pone.0108510. eCollection 2014.

使用基于干细胞的体外形态发生模型对常用辅料进行发育毒性评估。

Developmental toxicity assessment of common excipients using a stem cell-based in vitro morphogenesis model.

作者信息

Yuan Chloe J, Marikawa Yusuke

机构信息

University of Hawaii John A. Burns School of Medicine, Department of Anatomy, Biochemistry and Physiology, Institute for Biogenesis Research, Honolulu, HI, 96813, United States.

University of Hawaii John A. Burns School of Medicine, Department of Anatomy, Biochemistry and Physiology, Institute for Biogenesis Research, Honolulu, HI, 96813, United States.

出版信息

Food Chem Toxicol. 2017 Nov;109(Pt 1):376-385. doi: 10.1016/j.fct.2017.09.023. Epub 2017 Sep 18.

DOI:10.1016/j.fct.2017.09.023
PMID:28927898
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5656506/
Abstract

Various chemical compounds can inflict developmental toxicity when sufficiently high concentrations are exposed to embryos at the critical stages of development. Excipients, such as coloring agents and preservatives, are pharmacologically inactive ingredients that are included in various medications, foods, and cosmetics. However, concentrations that may adversely affect embryo development are largely unknown for most excipients. Here, the lowest observed adverse effect level (LOAEL) to inflict developmental toxicity was assessed for three coloring agents (allura red, brilliant blue, and tartrazine) and three preservatives (butylated hydroxyanisole, metabisulfite, and methylparaben). Adverse impact of a compound exposure was determined using the stem cell-based in vitro morphogenesis model, in which three-dimensional cell aggregates, or embryoid bodies (EBs), recapitulate embryonic processes of body axis elongation and patterning. LOAEL to impair EB morphogenesis was 200 μM for methylparaben, 400 μM for butylated hydroxyanisole, 600 μM for allura red and brilliant blue, and 1000 μM for metabisulfite. Gene expression analyses of excipient-treated EBs revealed that butylated hydroxyanisole and methylparaben significantly altered profiles of developmental regulators involved in axial elongation and patterning of the body. The present study may provide a novel in vitro approach to investigate potential developmental toxicity of common excipients with mechanistic insights.

摘要

当在发育的关键阶段将足够高浓度的各种化合物暴露于胚胎时,它们会造成发育毒性。辅料,如着色剂和防腐剂,是包含在各种药物、食品和化妆品中的药理惰性成分。然而,对于大多数辅料而言,可能对胚胎发育产生不利影响的浓度在很大程度上尚不清楚。在此,评估了三种着色剂(诱惑红、亮蓝和柠檬黄)和三种防腐剂(丁基羟基茴香醚、焦亚硫酸盐和对羟基苯甲酸甲酯)造成发育毒性的最低观察到有害作用水平(LOAEL)。使用基于干细胞的体外形态发生模型确定化合物暴露的不利影响,在该模型中,三维细胞聚集体或胚状体(EBs)概括了体轴伸长和模式形成的胚胎过程。对羟基苯甲酸甲酯损害EB形态发生的LOAEL为200μM,丁基羟基茴香醚为400μM,诱惑红和亮蓝为600μM,焦亚硫酸盐为1000μM。对辅料处理的EBs进行基因表达分析表明,丁基羟基茴香醚和对羟基苯甲酸甲酯显著改变了参与身体轴向伸长和模式形成的发育调节因子的谱。本研究可能提供一种新的体外方法,以深入了解常见辅料潜在的发育毒性及其作用机制。