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高脂肪饮食对非酒精性脂肪肝疾病小鼠模型肝脏基因表达谱的影响。

Impact of high-fat diet on liver genes expression profiles in mice model of nonalcoholic fatty liver disease.

机构信息

Department of Basic Veterinary Science, College of Veterinary Medicine, Northeast Agricultural University, Harbin 150030, PR China; Faculty of Life Science and Technology, Mudanjiang Normal University, Mudanjiang 157012, PR China.

Department of Basic Veterinary Science, College of Veterinary Medicine, Northeast Agricultural University, Harbin 150030, PR China; State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, Harbin 150001, PR China.

出版信息

Environ Toxicol Pharmacol. 2016 Jul;45:52-62. doi: 10.1016/j.etap.2016.05.014. Epub 2016 May 19.

Abstract

Evidences have shown that NAFLD influences expression of some drug metabolic enzyme genes. This study aims to investigate the role of HFD-induced NAFLD in regulating the transcription of genes, particularly the drug metabolizing genes variation. Transcriptome analysis demonstrated that HFD feeding caused the 150 genes expression to change, most genes associated with lipid metabolism, inflammatory, oxidative stress and oxidoreductase activity up-regulated, whereas most genes involved in nucleic acid metabolism repressed. The genes involved in drug metabolism had 16 down-regulated and 21 up-regulated in NAFLD. The over-4-fold change genes included the down-regulation of Cyp8b1, Cyp7a1, Sult3a1, Sult1e1, Cyp17a1, Cyp3a41a, Gstt3, Cyp51, Cyp2c54 and Cyp4f14, and the up-regulation of Asns, Past1, Cyp2c55, Gstm2, Cyp2e1 and Gstaα1. In conclusion, significant alterations in the expression of drug metabolizing enzymes may affect the clearance of therapeutic drugs, with the potential to result in adverse drug reactions or drug toxicity in nonalcoholic fatty liver disease.

摘要

有证据表明,NAFLD 会影响一些药物代谢酶基因的表达。本研究旨在探讨 HFD 诱导的 NAFLD 在调节基因转录中的作用,特别是药物代谢基因的变化。转录组分析表明,HFD 喂养导致 150 个基因的表达发生变化,大多数与脂质代谢、炎症、氧化应激和氧化还原酶活性相关的基因上调,而大多数与核酸代谢相关的基因受到抑制。参与药物代谢的基因中有 16 个下调和 21 个上调。变化超过 4 倍的基因包括 Cyp8b1、Cyp7a1、Sult3a1、Sult1e1、Cyp17a1、Cyp3a41a、Gstt3、Cyp51、Cyp2c54 和 Cyp4f14 的下调,以及 Asns、Past1、Cyp2c55、Gstm2、Cyp2e1 和 Gstaα1 的上调。总之,药物代谢酶表达的显著改变可能会影响治疗药物的清除率,从而导致非酒精性脂肪性肝病患者发生不良反应或药物毒性。

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