Pharmacokinetics of primary atractyligenin metabolites after coffee consumption

IF 4.9 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Nutritional Biochemistry Pub Date : 2025-05-01 Epub Date: 2025-02-15 DOI:10.1016/j.jnutbio.2025.109869
Roman Lang , Melanie Haas , Barbara Danzer , Veronika Somoza , Thomas Skurk
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Abstract

Coffee brew is an integral part of the individual diet worldwide. Roasted coffee contains numerous bioactive substances whose significance for health is investigated in nutritional studies. Food biomarkers are recommended to correlate coffee consumption and health effects in the most unbiased way possible. Metabolites of atractyligenin derivatives from roasted coffee have been suggested as candidate analytes indicating coffee consumption.
UHPLC-MS/MS analysis revealed that atractyligenin (1), 2-O-β-D-glucosylatractyligenin and 3′-O-β-D-glucosyl-2′-O-isovaleryl-2-O-β-D-glucosylatractyligenin were extracted into coffee brew. Their concentrations in filtered and unfiltered coffee did not differ significantly, suggesting independence from the preparation method.
In a coffee intervention study (n=12, female/male 6/6), atractyligenin metabolites were not detectable in plasma after three days of coffee abstinence. After coffee, atractyligenin (1) and atractyligenin-19-O-β-D-glucuronide (M1) were the quantitatively dominant atractyligenin metabolites in plasma and showed two peaks each after 0.5 and 10 h, respectively. Half-live of 1 after the first cmax in plasma was ∼0.31 h. 1 and M1 were detectable in plasma, indicating coffee consumption for up to 24 h after one serving.
Within 10 h, ∼13.7% of the atractyligenin glycosides supplied by coffee brew were excreted in urine as the metabolites 1 and M1. Metabolites 2β‑hydroxy-15-oxoatractylan-4α-carboxy-19-O-β-D-glucuronide (M2) and 2β‑hydroxy-15-oxoatractylan-4α-carboxylic acid-2-O-β-D-glucuronide (M3) were detected in only some samples and appeared unreliable as indicators for coffee consumption. No concentration differences between female and male study participants were observed in plasma and urine.
In conclusion atractyligenin and its 19-O-β-D-glucuronide are promising markers of Arabica coffee consumption in plasma and urine for both men and women, independent of the brewing method.
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咖啡饮用后原发苍木素代谢物的药代动力学。
咖啡是全世界个人饮食中不可或缺的一部分。烘焙咖啡含有大量的生物活性物质,其对健康的重要性在营养学研究中得到了调查。食物生物标志物被推荐以最公正的方式将咖啡消费与健康影响联系起来。从烘焙咖啡中产生的白术脂素衍生物的代谢物被认为是指示咖啡消费的候选分析物。UHPLC-MS/MS分析结果显示,从咖啡中提取了白术脂素(1)、2-O-β- d -葡萄糖酸丙基脂素和3'-O-β- d -葡萄糖酸丙基-2'-O-异戊酸-2-O-β- d -葡萄糖酸丙基脂素。它们在过滤咖啡和未过滤咖啡中的浓度没有显著差异,这表明它们与制备方法无关。在一项咖啡干预研究中(n=12,女性/男性6/6),戒掉咖啡三天后,血浆中检测不到苍术脂素代谢物。咖啡后,白术脂素(1)和白术脂素-19- o - d -葡萄糖醛酸酯(M1)是血浆中白术脂素代谢产物的数量优势,分别在0.5和10 h后出现两个峰。血浆中第一次cmax后的半衰期为~ 0.31 h。1和M1在血浆中可检测到,表明一次咖啡饮用后长达24小时。在10小时内,咖啡冲泡提供的白术脂素苷的约13.7%作为代谢物1和M1从尿液中排出。仅在部分样品中检测到代谢物2β-羟基-15- oxoatractyan -4α-羧酸-19- o -β-d-葡萄糖醛酸(M2)和2β-羟基-15- oxoatractyan -4α-羧酸-2- o -β-d-葡萄糖醛酸(M3),作为咖啡消费量的指标不可靠。女性和男性研究参与者在血浆和尿液中没有观察到浓度差异。综上所述,白术脂素及其19-O-β- d -葡糖苷是男性和女性血浆和尿液中阿拉比卡咖啡消费量的有希望的标志物,与冲泡方法无关。
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
Journal of Nutritional Biochemistry
Journal of Nutritional Biochemistry 医学-生化与分子生物学
CiteScore
9.50
自引率
3.60%
发文量
237
审稿时长
68 days
期刊介绍: Devoted to advancements in nutritional sciences, The Journal of Nutritional Biochemistry presents experimental nutrition research as it relates to: biochemistry, molecular biology, toxicology, or physiology. Rigorous reviews by an international editorial board of distinguished scientists ensure publication of the most current and key research being conducted in nutrition at the cellular, animal and human level. In addition to its monthly features of critical reviews and research articles, The Journal of Nutritional Biochemistry also periodically publishes emerging issues, experimental methods, and other types of articles.
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