人类细胞色素 P450 抑制数据在评估药物引起的肝损伤中的实用性。

IF 1.3 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Xenobiotica Pub Date : 2024-07-01 Epub Date: 2024-08-21 DOI:10.1080/00498254.2024.2312505
Shunnosuke Kaito, Jun-Ichi Takeshita, Misaki Iwata, Takamitsu Sasaki, Takuomi Hosaka, Ryota Shizu, Kouichi Yoshinari
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引用次数: 0

摘要

1.药物性肝损伤(DILI)是导致药物研发中止和撤出市场的一个主要原因,但目前还没有DILI风险评估的金标准方法。由于我们发现了 DILI 与 CYP1A1 或 CYP1B1 抑制之间的关联,因此我们利用决策树分析法进一步评估了细胞色素 P450(P450)抑制检测数据在 DILI 风险评估中的实用性。 使用重组酶和发光底物评估了有 DILI 风险的药物(DILI 药物)和无 DILI 风险的药物(无 DILI 药物)对 10 种人类 P450 的抑制活性。还使用 HepG2 细胞对这些药物进行了细胞毒性试验和高含量分析。分子描述符由 alvaDesc.3 计算得出。以获得的数据为变量,结合或不结合 P450 抑制活性进行决策树分析,以区分 DILI 药物和非 DILI 药物。加入 P450 抑制活性后,准确率明显提高。经过决策树判别后,再根据 P450 抑制活性进一步判别药物。结果表明,利用 P450 抑制活性数据可以正确区分许多假阳性和假阴性药物。 这些结果表明,P450 抑制活性检测数据有助于 DILI 风险评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Utility of human cytochrome P450 inhibition data in the assessment of drug-induced liver injury.

Drug-induced liver injury (DILI) is a major cause of drug development discontinuation and drug withdrawal from the market, but there are no golden standard methods for DILI risk evaluation. Since we had found the association between DILI and CYP1A1 or CYP1B1 inhibition, we further evaluated the utility of cytochrome P450 (P450) inhibition assay data for DILI risk evaluation using decision tree analysis.The inhibitory activity of drugs with DILI concern (DILI drugs) and no DILI concern (no-DILI drugs) against 10 human P450s was assessed using recombinant enzymes and luminescent substrates. The drugs were also subjected to cytotoxicity assays and high-content analysis using HepG2 cells. Molecular descriptors were calculated by alvaDesc.Decision tree analysis was performed with the data obtained as variables with or without P450-inhibitory activity to discriminate between DILI drugs and no-DILI drugs. The accuracy was significantly higher when P450-inhibitory activity was included. After the decision tree discrimination, the drugs were further discriminated with the P450-inhibitory activity. The results demonstrated that many false-positive and false-negative drugs were correctly discriminated by using the P450 inhibition data.These results suggest that P450 inhibition assay data are useful for DILI risk evaluation.

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来源期刊
Xenobiotica
Xenobiotica 医学-毒理学
CiteScore
3.80
自引率
5.60%
发文量
96
审稿时长
2 months
期刊介绍: Xenobiotica covers seven main areas, including:General Xenobiochemistry, including in vitro studies concerned with the metabolism, disposition and excretion of drugs, and other xenobiotics, as well as the structure, function and regulation of associated enzymesClinical Pharmacokinetics and Metabolism, covering the pharmacokinetics and absorption, distribution, metabolism and excretion of drugs and other xenobiotics in manAnimal Pharmacokinetics and Metabolism, covering the pharmacokinetics, and absorption, distribution, metabolism and excretion of drugs and other xenobiotics in animalsPharmacogenetics, defined as the identification and functional characterisation of polymorphic genes that encode xenobiotic metabolising enzymes and transporters that may result in altered enzymatic, cellular and clinical responses to xenobioticsMolecular Toxicology, concerning the mechanisms of toxicity and the study of toxicology of xenobiotics at the molecular levelXenobiotic Transporters, concerned with all aspects of the carrier proteins involved in the movement of xenobiotics into and out of cells, and their impact on pharmacokinetic behaviour in animals and manTopics in Xenobiochemistry, in the form of reviews and commentaries are primarily intended to be a critical analysis of the issue, wherein the author offers opinions on the relevance of data or of a particular experimental approach or methodology
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