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miR-150对药物代谢酶CYP3A4的调控作用

刘莉 彭金富 郭成贤 阳喜定 李海刚 阳国平

中国临床药理学与治疗学Issue(7):749-754,6.
中国临床药理学与治疗学Issue(7):749-754,6.DOI:10.12092/j.issn.1009-2501.2018.07.005

miR-150对药物代谢酶CYP3A4的调控作用

Regulative effects of miR-150 on CYP3A4

刘莉 1彭金富 2郭成贤 2阳喜定 3李海刚 1阳国平2

作者信息

  • 1. 长沙医学院药学院,长沙 410200,湖南
  • 2. 中南大学湘雅三医院,长沙 410013
  • 3. 中南大学湘雅二医院,长沙 410011,湖南
  • 折叠

摘要

Abstract

AIM:To explore the role of mi R-150 in the regulation of CYP3 A4 and the underlying mechanism.METHODS:CYP3 A4 m RNA and protein expression were tested by RT-PCR and Western blot when the Chang liver cells were stimulated by FFA containing fatty acids free 1% BSA.Bioinformatics mi RNA databases were used to identify CYP3 A4-related mi RNAs and the wild-type CYP3 A43'-UTR plasmids were constructed, mi R-150 and reporter plasmid were co-transfected into the Chang liver cells to test the expression ratio of the reported fluorescence and the correction fluorescence.Then the mi R-150 mimic were transfected into the Chang liver cells, while mi RNA inhibitor were transfected into the steatosis cells.RT-PCR and Western blot were used to detect CYP3 A4 m RNA and protein expression.RESULTS:The CYP3 A4 m RNA and protein level were statistically significantly decreased (P< 0.05), while the mature mi R-150 levels were increased (P < 0.05) when the Chang liver cells were stimulated after 24 h by 1 mmol/L FFA.CYP3 A4 was found to be the target gene of mi R-150 with a bioinformatics analysis.Then CYP3 A4 m RNA level was significantly decreased (P < 0.05).Meanwhile, the expression level of CYP3 A4 protein also decreased when the mi R-150 mimic were transfected into the Chang liver cells.But CYP3 A4 m RNA expression has no statistical significance (P = 0.071) in mi R-150 inhibitor group.CONCLUSION:The mi R-150 can combine with CYP3 A4 3'-UTR directly, and can further regulate the expression of CYP3 A4 m RNA.

关键词

miR-150/CYP3A4/调控作用

Key words

miR-150/CYP3A4/regulation

分类

医药卫生

引用本文复制引用

刘莉,彭金富,郭成贤,阳喜定,李海刚,阳国平..miR-150对药物代谢酶CYP3A4的调控作用[J].中国临床药理学与治疗学,2018,(7):749-754,6.

基金项目

湖南省教育厅科学研究项目资助(17C0169) (17C0169)

湖南省教育厅科学研究项目资助(15C0160) (15C0160)

国家自然科学基金(81373476) (81373476)

新型药物制剂研发湖南省重点实验室培育基地资助(2016TP1029) (2016TP1029)

中国临床药理学与治疗学

OACSCDCSTPCD

1009-2501

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