Perkins Edward J, Garcia-Reyero Natàlia, Villeneuve Daniel L, Martinovic Dalma, Brasfield Sandra M, Blake Lindsey S, Brodin Jeffrey D, Denslow Nancy D, Ankley Gerald T
Environmental Laboratory, US Army Engineer Research and Development Center, Vicksburg, MS 39180, USA.
Mar Environ Res. 2008 Jul;66(1):113-5. doi: 10.1016/j.marenvres.2008.02.072. Epub 2008 Mar 5.
Ketoconazole is a fungicidal drug that inhibits function of cytochrome P450s in the synthesis of steroids. To examine if inhibition of P450 function affects gene expression in a dynamic manner, we conducted in vitro exposures of ovary tissue from fathead minnows (Pimephales promelas) to 0.5 microM ketoconazole to investigate effects on steroid production and gene expression over time. Expression of four key steroidogenesis genes was examined at 1, 6, and 12h of exposure. 11 beta- and 20 beta-hydroxysteroid dehydrogenases were down regulated at 1h and Cytochrome P450 17 was down-regulated at 12h, consistent with the absence of steroid production. In contrast, cytochrome P450 19A was up-regulated at 6h, indicating feedback regulation. Microarray analysis of 12h exposures indicated enrichment of biological processes involved in neurotransmitter secretion, lymphocyte cell activation, sodium ion transport, and embryonic development. These data suggest that, with the exception of cytochrome P450 19A, these steroid metabolic genes are regulated in a feed forward manner and that the effects of ketoconazole may be broader than anticipated based on the mechanism of action alone.
酮康唑是一种具有杀菌作用的药物,它在类固醇合成过程中抑制细胞色素P450的功能。为了研究P450功能的抑制是否会动态影响基因表达,我们将黑头软口鲦鱼(Pimephales promelas)的卵巢组织在体外暴露于0.5微摩尔的酮康唑中,以研究随着时间推移对类固醇生成和基因表达的影响。在暴露1、6和12小时时检测了四个关键类固醇生成基因的表达。11β-和20β-羟基类固醇脱氢酶在1小时时下调,细胞色素P450 17在12小时时下调,这与类固醇生成的缺失一致。相比之下,细胞色素P450 19A在6小时时上调,表明存在反馈调节。对12小时暴露的微阵列分析表明,参与神经递质分泌、淋巴细胞活化、钠离子转运和胚胎发育的生物学过程有所富集。这些数据表明,除了细胞色素P450 19A外,这些类固醇代谢基因以前馈方式受到调节,并且酮康唑的作用可能比仅基于作用机制所预期的更为广泛。