Kalisch C, Reiter M, Mally A
Department of Toxicology, University of Würzburg, Versbacher Str. 9, 97078, Würzburg, Germany.
Arch Toxicol. 2025 Apr 4. doi: 10.1007/s00204-025-04022-2.
Humans are continuously exposed to furan, a hepatotoxic and carcinogenic process-related food contaminant. Considerable uncertainties associated with current exposure estimates based on the content of furan in food underscore the need to explore biomarker monitoring as an alternative or complementary approach to furan exposure assessment. Previous work in rats demonstrated a linear correlation between furan dose and several urinary furan metabolites, whereby N-[4-carboxy-4-(3-mercapto-1H-pyrrol-1-yl)-1-oxobutyl]-L-cysteinylglycine (GSH-BDA), the glutathione (GSH) conjugate of the reactive furan metabolite cis-2-butene-1,4-dial (BDA), was identified as a specific biomarker of exogenous furan exposure. To further test the validity of GSH-BDA as a biomarker of furan exposure, the present study was designed to monitor urinary excretion of furan metabolites in human volunteers after consumption of diets with low vs. high furan content using stable isotope dilution LC-MS/MS, and to investigate if analysis of GSH-BDA in human urine is suitable for translating biomarker levels into probable daily intakes. Ten healthy volunteers (n = 5/sex) consumed a low-furan diet for three days (day 1-3), followed by consumption of foods with high furan content for three days (day 4-6) and returned to a low-furan diet for a further three days (7-9). Urinary GSH-BDA excretion significantly increased during periods of a high-furan diet, and rapidly declined upon returning to a low-furan diet. Probable daily intakes estimated from GSH-BDA excretion in non-smoking subjects and excretion rates previously determined in F344/DuCrl rats ranged from 0.05 to 0.31 µg/kg bw/d during periods of low-furan diet and increased to 0.18-1.20 µg/kg bw/d during consumption of a high-furan diet. These estimates are in good agreement with exposures reported by the European Food Safety Authority (EFSA), which range between 0.11 to 0.75 µg/kg bw per day (minimum LB to maximum UB) for the average adult and 0.20 to 1.22 µg/kg bw per day (minimum LB to maximum UB) for highly exposed adult consumers (95th percentile). Interestingly, higher excretion of GSH-BDA was observed in smoking compared to non-smoking individuals, highlighting tobacco smoke as a significant source of furan exposure and confounding factor when estimating furan exposure via diet. In contrast to GSH-BDA, high urinary background levels of lysine adducts of BDA and BDA-derived cysteine-lysine crosslinks limit their suitability as biomarkers of exogenous furan exposure.
人类持续接触呋喃,这是一种与肝毒性和致癌过程相关的食品污染物。基于食品中呋喃含量的当前暴露估计存在相当大的不确定性,这突出表明需要探索生物标志物监测作为呋喃暴露评估的替代或补充方法。先前在大鼠身上进行的研究表明,呋喃剂量与几种尿中呋喃代谢物之间存在线性相关性,据此,N-[4-羧基-4-(3-巯基-1H-吡咯-1-基)-1-氧代丁基]-L-半胱氨酰甘氨酸(GSH-BDA),即活性呋喃代谢物顺式-2-丁烯-1,4-二醛(BDA)的谷胱甘肽(GSH)共轭物,被确定为外源性呋喃暴露的特异性生物标志物。为了进一步检验GSH-BDA作为呋喃暴露生物标志物的有效性,本研究旨在通过稳定同位素稀释液相色谱-串联质谱法监测人类志愿者食用低呋喃含量与高呋喃含量饮食后尿中呋喃代谢物的排泄情况,并研究分析人尿中的GSH-BDA是否适合将生物标志物水平转化为可能的每日摄入量。10名健康志愿者(男女各5名)食用低呋喃饮食3天(第1 - 3天),随后食用高呋喃含量食物3天(第4 - 6天),然后再食用低呋喃饮食3天(第7 - 9天)。在高呋喃饮食期间,尿中GSH-BDA排泄量显著增加,而恢复到低呋喃饮食后迅速下降。根据非吸烟受试者的GSH-BDA排泄量以及先前在F344/DuCrl大鼠中测定的排泄率估算的可能每日摄入量,在低呋喃饮食期间为0.05至0.31 μg/kg体重/天,在食用高呋喃饮食期间增加到0.18 - 1.20 μg/kg体重/天。这些估计值与欧洲食品安全局(EFSA)报告的暴露量高度一致,EFSA报告的平均成年人每日暴露量在0.11至0.75 μg/kg体重之间(最低下限到最高上限),高暴露成年消费者(第95百分位数)的每日暴露量在0.20至1.22 μg/kg体重之间(最低下限到最高上限)。有趣的是,与非吸烟个体相比,吸烟个体中观察到GSH-BDA的排泄量更高,这突出表明烟草烟雾是呋喃暴露的重要来源,也是通过饮食估算呋喃暴露时的混杂因素。与GSH-BDA不同,BDA的赖氨酸加合物和BDA衍生的半胱氨酸-赖氨酸交联物在尿中的背景水平较高,限制了它们作为外源性呋喃暴露生物标志物 的适用性。