时钟基因表达与CYP2C19、CYP3A4与苯二氮卓类药物的关系。

IF 2.7 4区 医学 Q3 TOXICOLOGY Human & Experimental Toxicology Pub Date : 2023-01-01 DOI:10.1177/09603271231171643
Naoto Tani, Tomoya Ikeda, Takaki Ishikawa
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引用次数: 0

摘要

本研究旨在阐明苯二氮卓类药物(BZD)患者体内参与药物代谢的时钟基因的表达和作用,以及各BZD类型中时钟基因控制的药物代谢调节因子。我们利用bzd尸检病例的肝脏研究时钟基因BMAL1、PER2和DBP的表达与药物代谢酶CYP3A4和CYP2C19的关系。此外,我们还检测了BZD暴露对HepG2人肝癌细胞中各种基因的影响。肝组织中DBP、CYP3A4、CYP2C19的表达在地西泮检测组低于未检测组。此外,BMAL1表达与CYP2C19表达相关。细胞培养实验显示,地西泮和咪达唑仑暴露后,DBP和CYP3A4的表达降低,BMAL1和CYP2C19的表达升高。尸检样本和培养细胞的分析结果表明,DBP在暴露于BZD时调节CYP3A4。了解这些生物钟基因和CYPs之间的关系可能有助于实现个体化药物治疗。
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Relationship between clock gene expression and CYP2C19 and CYP3A4 with benzodiazepines.

The present study aimed to clarify the expressions and roles of clock genes involved in drug metabolism in patients taking benzodiazepines (BZDs), as well as the drug metabolism regulators controlled by clock genes for each BZD type. The relationships between the expressions of the clock genes BMAL1, PER2, and DBP and the drug-metabolizing enzymes CYP3A4 and CYP2C19 were investigated using livers from BZD-detected autopsy cases. In addition, the effect of BZD exposure on various genes was examined in HepG2 human hepatocellular carcinoma cells. The expressions of DBP, CYP3A4, and CYP2C19 in the liver were lower in the diazepam-detected group than in the non-detected group. Furthermore, BMAL1 expression correlated with CYP2C19 expression. Cell culture experiments showed that the expressions of DBP and CYP3A4 decreased, whereas those of BMAL1 and CYP2C19 increased after diazepam and midazolam exposure. The results of the analyses of autopsy samples and cultured cells suggested that DBP regulates CYP3A4 when exposed to BZD. Understanding the relationship between these clock genes and CYPs may help achieve individualized drug therapy.

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来源期刊
CiteScore
5.70
自引率
3.60%
发文量
128
审稿时长
2.3 months
期刊介绍: Human and Experimental Toxicology (HET), an international peer reviewed journal, is dedicated to publishing preclinical and clinical original research papers and in-depth reviews that comprehensively cover studies of functional, biochemical and structural disorders in toxicology. The principal aim of the HET is to publish timely high impact hypothesis driven scholarly work with an international scope. The journal publishes on: Structural, functional, biochemical, and molecular effects of toxic agents; Studies that address mechanisms/modes of toxicity; Safety evaluation of novel chemical, biotechnologically-derived products, and nanomaterials for human health assessment including statistical and mechanism-based approaches; Novel methods or approaches to research on animal and human tissues (medical and veterinary patients) investigating functional, biochemical and structural disorder; in vitro techniques, particularly those supporting alternative methods
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