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对H295R细胞进行类固醇分析,以识别可能干扰肾上腺类固醇生成的化学物质。

Steroid profiling in H295R cells to identify chemicals potentially disrupting the production of adrenal steroids.

作者信息

Strajhar Petra, Tonoli David, Jeanneret Fabienne, Imhof Raphaella M, Malagnino Vanessa, Patt Melanie, Kratschmar Denise V, Boccard Julien, Rudaz Serge, Odermatt Alex

机构信息

Division of Molecular and Systems Toxicology, Department of Pharmaceutical Sciences, University of Basel, Klingelbergstrasse 50, 4056 Basel, Switzerland; Swiss Centre for Applied Human Toxicology (SCAHT), Universities of Basel and Geneva, Basel, Switzerland.

School of Pharmaceutical Sciences, University of Geneva and University of Lausanne, Pavillon des Isotopes 20, Boulevard d'Yvoy, 1211 Geneva, Switzerland; Swiss Centre for Applied Human Toxicology (SCAHT), Universities of Basel and Geneva, Basel, Switzerland.

出版信息

Toxicology. 2017 Apr 15;381:51-63. doi: 10.1016/j.tox.2017.02.010. Epub 2017 Feb 22.

Abstract

The validated OECD test guideline 456 based on human adrenal H295R cells promotes measurement of testosterone and estradiol production as read-out to identify potential endocrine disrupting chemicals. This study aimed to establish optimal conditions for using H295R cells to detect chemicals interfering with the production of key adrenal steroids. H295R cells' supernatants were characterized by liquid chromatography-mass spectrometry (LC-MS)-based steroid profiling, and the influence of experimental conditions including time and serum content was assessed. Steroid profiles were determined before and after incubation with reference compounds and chemicals to be tested for potential disruption of adrenal steroidogenesis. The H295R cells cultivated according to the OECD test guideline produced progestins, glucocorticoids, mineralocorticoids and adrenal androgens but only very low amounts of testosterone. However, testosterone contained in Nu-serum was metabolized during the 48h incubation. Thus, inclusion of positive and negative controls and a steroid profile of the complete medium prior to the experiment (t=0h) was necessary to characterize H295R cells' steroid production and indicate alterations caused by exposure to chemicals. Among the tested chemicals, octyl methoxycinnamate and acetyl tributylcitrate resembled the corticosteroid induction pattern of the positive control torcetrapib. Gene expression analysis revealed that octyl methoxycinnamate and acetyl tributylcitrate enhanced CYP11B2 expression, although less pronounced than torcetrapib. Further experiments need to assess the toxicological relevance of octyl methoxycinnamate- and acetyl tributylcitrate-induced corticosteroid production. In conclusion, the extended profiling and appropriate controls allow detecting chemicals that act on steroidogenesis and provide initial mechanistic evidence for prioritizing chemicals for further investigations.

摘要

基于人肾上腺H295R细胞的经验证的经合组织测试指南456促进了睾酮和雌二醇生成量的测量,以此作为识别潜在内分泌干扰化学物质的指标。本研究旨在确定使用H295R细胞检测干扰关键肾上腺类固醇生成的化学物质的最佳条件。通过基于液相色谱 - 质谱(LC-MS)的类固醇谱分析对H295R细胞的上清液进行表征,并评估包括时间和血清含量在内的实验条件的影响。在与参考化合物和待测化学物质孵育之前和之后测定类固醇谱,以检测对肾上腺类固醇生成的潜在干扰。按照经合组织测试指南培养的H295R细胞产生孕激素、糖皮质激素、盐皮质激素和肾上腺雄激素,但睾酮产量极低。然而,Nu - 血清中的睾酮在48小时孵育期间被代谢。因此,在实验前(t = 0小时)纳入阳性和阴性对照以及完全培养基的类固醇谱对于表征H295R细胞的类固醇生成并指示化学物质暴露引起的变化是必要的。在所测试的化学物质中,甲氧基肉桂酸辛酯和乙酰柠檬酸三丁酯类似于阳性对照托彻普贝的皮质类固醇诱导模式。基因表达分析表明,甲氧基肉桂酸辛酯和乙酰柠檬酸三丁酯增强了CYP11B2的表达,尽管不如托彻普贝明显。进一步的实验需要评估甲氧基肉桂酸辛酯和乙酰柠檬酸三丁酯诱导的皮质类固醇生成的毒理学相关性。总之,扩展的谱分析和适当的对照能够检测作用于类固醇生成的化学物质,并为优先选择化学物质进行进一步研究提供初步的机制证据。

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