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建立一个真实的人体皮肤模型,用于研究苯并[a]芘的皮肤吸收,以确定与致癌暴露最相关的生物标志物。

A realistic human skin model to study benzo[a]pyrene cutaneous absorption in order to determine the most relevant biomarker for carcinogenic exposure.

机构信息

Equipe Environnement et Prédiction de la Santé des Populations, Faculté de Médecine, Laboratoire TIMC-IMAG (UMR 5525 UGA-CNRS), Université Grenoble Alpes, 38706, La Tronche, France.

Service de Biochimie Biologie moléculaire Toxicologie de l'Environnement, Unité Médicale de Toxicologie Professionnelle et Environnementale, CHU Grenoble Alpes, 38000, Grenoble, France.

出版信息

Arch Toxicol. 2019 Jan;93(1):81-93. doi: 10.1007/s00204-018-2329-2. Epub 2018 Oct 22.

Abstract

Polycyclic aromatic hydrocarbons (PAH) are ubiquitous pollutants, among which benzo[a]pyrene (B[a]P) is the only compound classified carcinogenic to humans. Besides pulmonary uptake, skin is the major route of PAH absorption during occupational exposure. Health risk due to PAH exposure is commonly assessed among workers using biomonitoring. A realistic human ex vivo skin model was developed to explore B[a]P diffusion and metabolism to determine the most relevant biomarker following dermal exposure. Three realistic doses (0.88, 8.85 and 22.11 nmol/cm) were topically applied for 8, 24, and 48 h. B[a]P and its metabolites were quantified by liquid chromatography coupled with fluorimetric detection. The impact of time, applied dose, and donor age were estimated using a linear mixed-effects model. B[a]P vastly penetrated the skin within 8 h. The major metabolites were 3-hydroxybenzo[a]pyrene (3-OHB[a]P) and 7,8,9,10-tetrahydroxy-7,8,9,10-tetrahydrobenzo[a]pyrene (B[a]P-tetrol). This latter predominantly derives from the most carcinogenic metabolite of B[a]P, benzo[a]pyrene-7,8-diol-9,10-epoxide (BPDE), as well as benzo[a]pyrene-9,10-diol-7,8-epoxide (reverse-BPDE). Benzo[a]pyrene-trans-7,8-dihydrodiol (B[a]P-7,8-diol) was a minor metabolite, and benzo[a]pyrene-trans-4,5-dihydrodiol (B[a]P-4,5-diol) was never quantified. Unmetabolized B[a]P bioavailability was limited following dermal exposure since less than 3% of the applied dose could be measured in the culture medium. B[a]P was continuously absorbed and metabolized by human skin over 48 h. B[a]P-tetrol production became saturated as the applied dose increased, while no effect was measured on the other metabolic pathways. Age had a slight positive effect on B[a]P absorption and metabolism. This work supports the relevance of B[a]P-tetrol to assess occupational exposure and carcinogenic risk after cutaneous absorption of B[a]P.

摘要

多环芳烃(PAH)是普遍存在的污染物,其中苯并[a]芘(B[a]P)是唯一被归类为人类致癌物的化合物。除了肺部摄取外,皮肤是职业暴露期间 PAH 吸收的主要途径。通常使用生物监测来评估职业暴露于 PAH 的健康风险。为了探索 B[a]P 的扩散和代谢,以确定皮肤暴露后最相关的生物标志物,开发了一种现实的人体离体皮肤模型。三种现实剂量(0.88、8.85 和 22.11 nmol/cm)分别在 8、24 和 48 小时内进行局部应用。通过液相色谱-荧光检测定量分析 B[a]P 及其代谢产物。使用线性混合效应模型估计时间、应用剂量和供体年龄的影响。B[a]P 在 8 小时内大量穿透皮肤。主要代谢产物为 3-羟基苯并[a]芘(3-OHB[a]P)和 7,8,9,10-四羟基-7,8,9,10-四氢苯并[a]芘(B[a]P-四醇)。后者主要来自 B[a]P 最具致癌性的代谢物苯并[a]芘-7,8-二醇-9,10-环氧化物(BPDE)以及苯并[a]芘-9,10-二醇-7,8-环氧化物(反向-BPDE)。苯并[a]芘-反-7,8-二氢二醇(B[a]P-7,8-二醇)是一种次要代谢产物,而苯并[a]芘-反-4,5-二氢二醇(B[a]P-4,5-二醇)从未被定量。由于可在培养基中测量的应用剂量不到 3%,因此皮肤暴露后未代谢的 B[a]P 生物利用度有限。B[a]P 在 48 小时内持续被人体皮肤吸收和代谢。随着应用剂量的增加,B[a]P-四醇的产生达到饱和,而其他代谢途径则没有影响。年龄对 B[a]P 的吸收和代谢有轻微的积极影响。这项工作支持 B[a]P-四醇作为评估职业暴露和皮肤吸收 B[a]P 后致癌风险的相关性。

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