Elucidating the Metabolism of Chiral PCB95 in Wildtype and Transgenic Mouse Models with Altered Cytochrome P450 Enzymes Using Intestinal Content Screening.

IF 3.7 3区 医学 Q2 CHEMISTRY, MEDICINAL
Chemical Research in Toxicology Pub Date : 2024-12-16 Epub Date: 2024-11-19 DOI:10.1021/acs.chemrestox.4c00350
Xueshu Li, Amanda J Bullert, Binita Gautam, Weiguo Han, Weizhu Yang, Qing-Yu Zhang, Xinxin Ding, Hans-Joachim Lehmler
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引用次数: 0

Abstract

Polychlorinated biphenyls (PCBs), such as 2,2',3,5',6-pentachlorobiphenyl (PCB95), are persistent organic pollutants associated with adverse health outcomes, including developmental neurotoxicity. PCB95 is a chiral neurotoxic PCB congener atropselectively metabolized to potentially neurotoxic metabolites in vivo. However, the metabolic pathways of most PCB congeners, including PCB95, remain unknown. To address this knowledge gap, we analyzed the intestinal contents of mice exposed to PCB95 to elucidate the PCB95 metabolism pathway and assess if genetic manipulation of hepatic drug-metabolizing enzymes affects PCB95 metabolism. Our study exposed male and female wildtype (WT), Cyp2abfgs-null (KO), and CYP2A6-transgenic/Cyp2abfgs-null (KI) mice orally to 1.0 mg/kg body weight of PCB95. Intestinal content was collected 24 h after PCB administration. aS-PCB95 was enriched in all intestinal content samples, irrespective of sex and genotype. Gas chromatography-tandem mass spectrometry (GC-MS/MS) analyses identified 5 mono- (OH-PCB95) and 4 dihydroxylated PCB (diOH-PCB95) metabolites. Liquid chromatography-high-resolution mass spectrometry (LC-HRMS) identified 15 polar hydroxylated, methoxylated, and sulfated PCB95 metabolites, including 3 dechlorinated metabolites. A sex difference in the relative OH-PCB95 levels was observed only for KO in the LC-HRMS analysis. Genotype-dependent differences were observed for female, but not male, mice, with OH-PCB95 levels in female KO (FKO) mice tending to be lower than those in female WT (FWT) and KI (FKI) mice. Based on the GC-MS/MS analysis, these differences are due to the unknown PCB95 metabolites, X1-95 and Y1-95. These findings demonstrate that combining GC-MS/MS analyses and LC-HRMS subject screening of the intestinal content of PCB95-exposed mice can significantly advance our understanding of PCB95 metabolism in vivo.

利用肠道内容物筛查阐明手性 PCB95 在细胞色素 P450 酶发生变化的野生型和转基因小鼠模型中的代谢。
多氯联苯(PCB),如 2,2',3,5',6-五氯联苯(PCB95),是一种与不良健康后果(包括发育神经毒性)相关的持久性有机污染物。PCB95 是一种手性神经毒性多氯联苯同系物,在体内可选择性地代谢成潜在的神经毒性代谢物。然而,包括 PCB95 在内的大多数多氯联苯同系物的代谢途径仍然未知。为了填补这一知识空白,我们分析了暴露于 PCB95 的小鼠的肠道内容物,以阐明 PCB95 的代谢途径,并评估肝脏药物代谢酶的遗传操作是否会影响 PCB95 的代谢。我们的研究让雄性和雌性野生型(WT)、Cyp2abfgs-null(KO)和 CYP2A6 转基因/Cyp2abfgs-null(KI)小鼠口服 1.0 毫克/千克体重的 PCB95。aS-PCB95 在所有肠道样本中都有富集,与性别和基因型无关。气相色谱-串联质谱(GC-MS/MS)分析确定了 5 种单羟基多氯联苯(OH-PCB95)和 4 种二羟基多氯联苯(diOH-PCB95)代谢物。液相色谱-高分辨质谱法(LC-HRMS)确定了 15 种极性羟基化、甲氧基化和硫酸化 PCB95 代谢物,包括 3 种脱氯代谢物。在 LC-HRMS 分析中,只观察到 KO 的 OH-PCB95 相对水平存在性别差异。雌性小鼠的 OH-PCB95 水平往往低于 WT(FWT)和 KI(FKI)雌性小鼠。根据 GC-MS/MS 分析,这些差异是由于未知的 PCB95 代谢物 X1-95 和 Y1-95 造成的。这些研究结果表明,结合 GC-MS/MS 分析和 LC-HRMS 主题筛选暴露于 PCB95 的小鼠肠道内容物,可以极大地促进我们对 PCB95 体内代谢的了解。
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
7.90
自引率
7.30%
发文量
215
审稿时长
3.5 months
期刊介绍: Chemical Research in Toxicology publishes Articles, Rapid Reports, Chemical Profiles, Reviews, Perspectives, Letters to the Editor, and ToxWatch on a wide range of topics in Toxicology that inform a chemical and molecular understanding and capacity to predict biological outcomes on the basis of structures and processes. The overarching goal of activities reported in the Journal are to provide knowledge and innovative approaches needed to promote intelligent solutions for human safety and ecosystem preservation. The journal emphasizes insight concerning mechanisms of toxicity over phenomenological observations. It upholds rigorous chemical, physical and mathematical standards for characterization and application of modern techniques.
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