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首页> 外文期刊>Toxicologic pathology >Characterization of polybrominated diphenyl ether toxicity in wistar han rats and use of liver microarray data for predicting disease susceptibilities
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Characterization of polybrominated diphenyl ether toxicity in wistar han rats and use of liver microarray data for predicting disease susceptibilities

机译:wistar han大鼠中多溴联苯醚毒性的表征以及肝脏微阵列数据在预测疾病易感性中的应用

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The toxicity of polybrominated diphenyl ethers (PBDEs), flame-retardant components, was characterized in offspring from Wistar Han dams exposed by gavage to a PBDE mixture (DE71) starting at gestation day 6 and continuing to weaning on postnatal day (PND) 21. Offspring from the dams underwent PBDE direct dosing by gavage at the same dose as their dams from PND 12 to PND 21, and then after weaning for another thirteen weeks. Liver samples were collected at PND 22 and week 13 for liver gene expression analysis (Affymetrix Rat Genome 230 2.0 Array). Treatment with PBDE induced 1,066 liver gene transcript changes in females and 1,200 transcriptional changes in males at PND 22 (false discovery rate < 0.01), but only 263 liver transcriptional changes at thirteen weeks in male rats (false discovery rate < 0.05). No significant differences in dose response were found between male and female pups. Transcript changes at PND 22 coded for proteins in xenobiotic, sterol, and lipid metabolism, and cell cycle regulation, and overlapped rodent liver transcript patterns after a high-fat diet or phenobarbital exposure. These findings, along with the observed PBDE-induced liver hypertrophy and vacuolization, suggest that long-term PBDE exposure has the potential to modify cell functions that contribute to metabolic disease and/or cancer susceptibilities.
机译:多溴联苯醚(PBDEs)是阻燃剂的毒性,其特征是Wistar Han大坝的后代从管胎暴露于PBDE混合物(DE71),从妊娠第6天开始,到出生后第21天继续断奶。水坝的后代通过强饲法以与水坝相同的剂量从PND 12到PND 21进行PBDE直接给药,然后在断奶后再维持13周。在PND 22和第13周收集肝样品用于肝基因表达分析(Affymetrix Rat Genome 230 2.0 Array)。在PND 22时,PBDE处理可诱导雌性1,066肝基因转录物变化,雄性导致1200转录变化(假发现率<0.01),但在雄性大鼠的第13周,仅263肝脏转录变化(假发现率<0.05)。雄性和雌性幼崽之间在剂量反应方面没有发现显着差异。在高脂饮食或苯巴比妥暴露后,PND 22的转录本变化编码为异种生物,固醇和脂质代谢以及细胞周期调节中的蛋白质,并且与啮齿动物肝脏的转录方式重叠。这些发现以及观察到的PBDE诱导的肝肥大和空泡化表明,长期暴露于PBDE可能会改变导致代谢疾病和/或癌症易感性的细胞功能。

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