The Cytochrome P450 2C8*3 Variant (rs11572080) Is Associated with Improved Asthma Symptom Control in Children and Altered Lipid Mediator Production and Inflammatory Response in Human Bronchial Epithelial Cells.

IF 4.4 3区 医学 Q1 PHARMACOLOGY & PHARMACY Drug Metabolism and Disposition Pub Date : 2024-07-16 DOI:10.1124/dmd.124.001684
Marysol Almestica-Roberts, Nam D Nguyen, Lili Sun, Samantha N Serna, Emmanuel Rapp, Katherine L Burrell-Gerbers, Tosifa A Memon, Bryan L Stone, Flory L Nkoy, John G Lamb, Cassandra E Deering-Rice, Joseph E Rower, Christopher A Reilly
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Abstract

This study investigated an association between the cytochrome P450 (CYP) 2C8*3 polymorphism with asthma symptom control in children and changes in lipid metabolism and pro-inflammatory signaling by human bronchial epithelial cells (HBECs) treated with cigarette smoke condensate (CSC). CYP genes are inherently variable in sequence, and while such variations are known to produce clinically relevant effects on drug pharmacokinetics and pharmacodynamics, the effects on endogenous substrate metabolism and associated physiologic processes are less understood. In this study, CYP2C8*3 was associated with improved asthma symptom control among children: Mean asthma control scores were 3.68 (n = 207) for patients with one or more copies of the CYP2C8*3 allele versus 4.42 (n = 965) for CYP2C8*1/*1 (P = 0.0133). In vitro, CYP2C8*3 was associated with an increase in montelukast 36-hydroxylation and a decrease in linoleic acid metabolism despite lower mRNA and protein expression. Additionally, CYP2C8*3 was associated with reduced mRNA expression of interleukin-6 (IL-6) and C-X-C motif chemokine ligand 8 (CXCL-8) by HBECs in response to CSC, which was replicated using the soluble epoxide hydrolase inhibitor, 12-[[(tricyclo[3.3.1.13,7]dec-1-ylamino)carbonyl]amino]-dodecanoic acid. Interestingly, 9(10)- and 12(13)- dihydroxyoctadecenoic acid, the hydrolyzed metabolites of 9(10)- and 12(13)- epoxyoctadecenoic acid, increased the expression of IL-6 and CXCL-8 mRNA by HBECs. This study reveals previously undocumented effects of the CYP2C8*3 variant on the response of HBECs to exogenous stimuli. SIGNIFICANCE STATEMENT: These findings suggest a role for CYP2C8 in regulating the epoxyoctadecenoic acid:dihydroxyoctadecenoic acid ratio leading to a change in cellular inflammatory responses elicited by environmental stimuli that exacerbate asthma.

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细胞色素 P450 (CYP) 2C8*3 变异(rs11572080)与儿童哮喘症状控制的改善以及人类支气管上皮细胞脂质介质生成和炎症反应的改变有关。
本研究调查了细胞色素 P450(CYP)2C8*3 多态性与儿童哮喘症状控制之间的关系,以及经香烟烟雾冷凝物(CSC)处理的人类支气管上皮细胞(HBECs)在脂质代谢和促炎症信号转导方面的变化。CYP 基因在序列上具有固有的可变性,虽然已知这种变异会对药物的药代动力学和药效学产生临床相关的影响,但对内源性底物代谢和相关生理过程的影响却不甚了解。在这项研究中,CYP2C8*3 与儿童哮喘症状控制的改善有关:具有一个或多个 CYP2C8*3 等位基因拷贝的患者的平均哮喘控制评分为 3.68 [n=207] 分,而具有 CYP2C8*1/*1 等位基因拷贝的患者的平均哮喘控制评分为 4.42 [n=965] 分(p=0.0133)。在体外,CYP2C8*3 与孟鲁司特 36- 羟基化的增加和亚油酸(LA)代谢的减少有关,尽管其 mRNA 和蛋白表达较低。此外,CYP2C8*3 与 HBECs 对 CSC 反应时白细胞介素-6(IL-6)和 C-X-C motif 趋化因子配体 8(CXCL-8)的 mRNA 表达减少有关,使用可溶性环氧化物水解酶抑制剂 AUDA 复制了这一结果。有趣的是,9(10)- 和 12(13)-EpOME 的水解代谢产物 9(10)- 和 12(13)-DiHOME 增加了 HBECs IL-6 和 CXCL-8 mRNA 的表达。这项研究揭示了 CYP2C8*3 变体对 HBECs 对外源刺激反应的影响,而这种影响以前未被记录。意义声明 这些研究结果表明,CYP2C8 在调节 EpOME:DiHOME 比率中的作用导致了由环境刺激引起的细胞炎症反应的变化,而环境刺激会加重哮喘。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.50
自引率
12.80%
发文量
128
审稿时长
3 months
期刊介绍: An important reference for all pharmacology and toxicology departments, DMD is also a valuable resource for medicinal chemists involved in drug design and biochemists with an interest in drug metabolism, expression of drug metabolizing enzymes, and regulation of drug metabolizing enzyme gene expression. Articles provide experimental results from in vitro and in vivo systems that bring you significant and original information on metabolism and disposition of endogenous and exogenous compounds, including pharmacologic agents and environmental chemicals.
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