Tiboni Gian Mario, Marotta Francesca, Carletti Erminia
Sezione di Ostetricia e Ginecologia, Dipartimento di Medicina e Scienze dell'Invecchiamento, Facoltà di Medicina e Chirurgia, Università G. d'Annunzio di Chieti-Pescara, Italy.
Reprod Toxicol. 2009 Apr;27(2):199-202. doi: 10.1016/j.reprotox.2009.01.001. Epub 2009 Jan 21.
Disruption of embryonal retinoic acid homeostasis has been postulated to represent an etiological factor involved in the onset of fluconazole-induced teratogenesis. In the present study the impact of a teratogenic pulse of fluconazole on the gene expression of cytochrome P450 (CYP) 26 isoforms, which plays a central role in maintaining proper retinoic acid levels by mediating its degradation, was investigated. ICR pregnant mice were orally administered with 0 (vehicle) or 700mg/kg of fluconazole on gestation day 8. Embryos were collected 12, 24 and 48h after treatment. Quantitative real-time reverse-transcription polymerase chain reaction (quantitative real-time RT-PCR) assay was used to quantify the mRNA expression of CYP26a1, CYP26b1 and CYP26c1 in embryos. As result, fluconazole exposure was associated to an up-regulation of CYP26a1, CYP26b1, whereas no significant change was identified for the CYP26c1 isoform. This study demonstrates the capacity of fluconazole to alter CYP26 gene expression in mouse embryos.
胚胎维甲酸稳态的破坏被认为是氟康唑诱导致畸作用发生的一个病因学因素。在本研究中,研究了氟康唑致畸脉冲对细胞色素P450(CYP)26亚型基因表达的影响,该亚型通过介导维甲酸降解在维持适当的维甲酸水平中起核心作用。在妊娠第8天,对ICR怀孕小鼠口服给予0(赋形剂)或700mg/kg氟康唑。在处理后12、24和48小时收集胚胎。采用定量实时逆转录聚合酶链反应(定量实时RT-PCR)测定法对胚胎中CYP26a1、CYP26b1和CYP26c1的mRNA表达进行定量。结果显示,氟康唑暴露与CYP26a1、CYP26b1的上调有关,而CYP26c1亚型未发现显著变化。本研究证明了氟康唑改变小鼠胚胎中CYP26基因表达的能力。