内分泌干扰效应模型:人类胎盘类固醇生成

IF 2.7 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Line Mathiesen, Dea Sandal, Ida Elise Moelgaard Hammer, Bjarne Styrishave, Lisbeth E. Knudsen
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引用次数: 0

摘要

随着流行病学研究报告暴露与胎儿生长不良影响的关联,怀孕期间的内分泌干扰引起了越来越多的关注,随后对正在成长的儿童产生影响,最终对成人产生影响。在研究妊娠期内分泌干扰时,由于人类胎盘具有独特的细胞摄取胆固醇、高水平孕酮产生和芳香化酶表达的途径,因此很难建立胎盘类固醇生成的模型。测试内分泌干扰的模型应尊重物种差异,优先于人类风险评估的人类模型。在这里,我们介绍了现有的关于胎盘甾体形成和其他胎盘激素的研究,包括:胎盘灌注、胎盘外植体、碎片、微粒体和囊泡、原代细胞培养、干细胞、胎盘芯片和绒毛膜癌细胞培养:BeWo、HTR-8/SVneo、Jar、JEG-3和ACH-3P。我们得出的结论是,缺乏对胎盘类固醇生成和内分泌干扰化合物影响的研究。讨论了现有模型的优点和局限性,并提出了未来的发展方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Models of Endocrine-Disrupting Effects: Human Placental Steroidogenesis

Models of Endocrine-Disrupting Effects: Human Placental Steroidogenesis

Endocrine disruption during pregnancy has gained increasing interest as epidemiological studies report associations of exposures and adverse effects on fetal growth, followed by effects on the growing child and ultimately in the adult. When studying endocrine disruption during pregnancy, the placental steroidogenesis is difficult to model, as the human placenta is unique in the pathway of cellular uptake of cholesterol, the high levels of progesterone production and the expression of aromatase. Models to test for endocrine disruption should respect species differences, with preference to human models for human risk assessment. Here, we present existing research of placental steroidogenesis and other placental hormones using human placental models: placental perfusion, placental explants, fragments, microsomes and vesicles, primary cell culture, stem cells, placenta on a chip and choriocarcinoma cell cultures: BeWo, HTR-8/SVneo, Jar, JEG-3 and ACH-3P. We conclude that there is a lack of research focused on placental steroidogenesis and the effects of endocrine-disrupting compounds. Advantages and limitations of existing models are discussed, and future directions suggested.

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来源期刊
CiteScore
5.60
自引率
6.50%
发文量
126
审稿时长
1 months
期刊介绍: Basic & Clinical Pharmacology and Toxicology is an independent journal, publishing original scientific research in all fields of toxicology, basic and clinical pharmacology. This includes experimental animal pharmacology and toxicology and molecular (-genetic), biochemical and cellular pharmacology and toxicology. It also includes all aspects of clinical pharmacology: pharmacokinetics, pharmacodynamics, therapeutic drug monitoring, drug/drug interactions, pharmacogenetics/-genomics, pharmacoepidemiology, pharmacovigilance, pharmacoeconomics, randomized controlled clinical trials and rational pharmacotherapy. For all compounds used in the studies, the chemical constitution and composition should be known, also for natural compounds.
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