Antifungal climbazole alters androgenic pathways in mammalian cells

IF 2.6 3区 医学 Q3 TOXICOLOGY
Dieynaba Ndiaye, Marie Perceau, Mylène Lorcin, Flavien Denis, Laurent Gaté
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引用次数: 0

Abstract

Among antifungal agents used in pharmaceuticals and personal care products, the synthetic azole climbazole (CBZ; 1-(4-Chlorophenoxy)-1-(imidazol-1-yl)-3,3-dimethylbutan-2-one) acts on the fungus Malassezia. Despite concerns surrounding its effects on health, based on alterations to reproduction and steroidogenesis found in fish, little is known about its mechanism of action as an endocrine disrupting chemical (EDC) in mammalian cells.

In this study, using OECD test guidelines, we investigated the effects of CBZ (i) in H295R cells, on the production of estradiol and testosterone, as well as intermediate metabolites in steroidogenesis pathway, and (ii) in HeLa9903 and AR-EcoScreen cell lines, on the transactivation of estrogen and androgen receptors.

Our results are the first evidence in H295R cells, that CBZ treatment (from 0.3 μM) decreased secreted levels of testosterone and estradiol. This was associated with reduced 17α-hydroxypregnenolone and 17α-hydroxyprogesterone levels. The altered levels of these metabolites were associated with a decrease in cytochrome P450 17α-hydroxylase/17,20-lyase (Cyp17A1) activity without any effect on its protein level. CBZ was also found to exert antagonistic effects toward androgen and estrogen α receptors. These results give insights into the toxicological mechanism of action of CBZ. Many azoles share structural similarities; therefore, caution should be adopted due to their potential toxicity.

抗真菌剂康巴唑改变哺乳动物细胞中的雄激素通路
在药品和个人护理产品中使用的抗真菌剂中,合成唑类攀唑(CBZ;1-(4-氯苯氧基)-1-(咪唑-1-基)-3,3-二甲基丁-2-酮)可作用于马拉色菌。尽管人们担心它对健康的影响,因为它改变了鱼类的生殖和类固醇生成,但人们对它作为内分泌干扰化学物质(EDC)在哺乳动物细胞中的作用机制却知之甚少。在这项研究中,我们采用 OECD 测试指南,研究了 CBZ(i)在 H295R 细胞中对雌二醇和睾酮以及类固醇生成途径中的中间代谢产物产生的影响,以及(ii)在 HeLa9903 和 AR-EcoScreen 细胞系中对雌激素和雄激素受体转活的影响。这与 17α-hydroxypregnenolone 和 17α-hydroxyprogesterone 水平的降低有关。这些代谢物水平的改变与细胞色素 P450 17α- 羟化酶/17,20-赖氨酸酶(Cyp17A1)活性的降低有关,但对其蛋白质水平没有任何影响。还发现 CBZ 对雄激素和雌激素 α 受体有拮抗作用。这些结果使人们对 CBZ 的毒理学作用机制有了更深入的了解。许多唑类药物结构相似,因此应谨慎使用,以免产生潜在毒性。
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来源期刊
Toxicology in Vitro
Toxicology in Vitro 医学-毒理学
CiteScore
6.50
自引率
3.10%
发文量
181
审稿时长
65 days
期刊介绍: Toxicology in Vitro publishes original research papers and reviews on the application and use of in vitro systems for assessing or predicting the toxic effects of chemicals and elucidating their mechanisms of action. These in vitro techniques include utilizing cell or tissue cultures, isolated cells, tissue slices, subcellular fractions, transgenic cell cultures, and cells from transgenic organisms, as well as in silico modelling. The Journal will focus on investigations that involve the development and validation of new in vitro methods, e.g. for prediction of toxic effects based on traditional and in silico modelling; on the use of methods in high-throughput toxicology and pharmacology; elucidation of mechanisms of toxic action; the application of genomics, transcriptomics and proteomics in toxicology, as well as on comparative studies that characterise the relationship between in vitro and in vivo findings. The Journal strongly encourages the submission of manuscripts that focus on the development of in vitro methods, their practical applications and regulatory use (e.g. in the areas of food components cosmetics, pharmaceuticals, pesticides, and industrial chemicals). Toxicology in Vitro discourages papers that record reporting on toxicological effects from materials, such as plant extracts or herbal medicines, that have not been chemically characterized.
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