Department of Nutrition, Norwich Medical School, University of East Anglia, Norwich, United Kingdom.
Am J Clin Nutr. 2013 May;97(5):995-1003. doi: 10.3945/ajcn.112.049247.
Evidence suggests that the consumption of anthocyanin-rich foods beneficially affects cardiovascular health; however, the absorption, distribution, metabolism, and elimination (ADME) of anthocyanin-rich foods are relatively unknown.
We investigated the ADME of a (13)C5-labeled anthocyanin in humans.
Eight male participants consumed 500 mg isotopically labeled cyanidin-3-glucoside (6,8,10,3',5'-(13)C5-C3G). Biological samples were collected over 48 h, and (13)C and (13)C-labeled metabolite concentrations were measured by using isotope-ratio mass spectrometry and liquid chromatography-tandem mass spectrometry.
The mean ± SE percentage of (13)C recovered in urine, breath, and feces was 43.9 ± 25.9% (range: 15.1-99.3% across participants). The relative bioavailability was 12.38 ± 1.38% (5.37 ± 0.67% excreted in urine and 6.91 ± 1.59% in breath). Maximum rates of (13)C elimination were achieved 30 min after ingestion (32.53 ± 14.24 μg(13)C/h), whereas (13)C-labeled metabolites peaked (maximum serum concentration: 5.97 ± 2.14 μmol/L) at 10.25 ± 4.14 h. The half-life for (13)C-labeled metabolites ranged between 12.44 ± 4.22 and 51.62 ± 22.55 h. (13)C elimination was greatest between 0 and 1 h for urine (90.30 ± 15.28 μg/h), at 6 h for breath (132.87 ± 32.23 μg/h), and between 6 and 24 h for feces (557.28 ± 247.88 μg/h), whereas the highest concentrations of (13)C-labeled metabolites were identified in urine (10.77 ± 4.52 μmol/L) and fecal samples (43.16 ± 18.00 μmol/L) collected between 6 and 24 h. Metabolites were identified as degradation products, phenolic, hippuric, phenylacetic, and phenylpropenoic acids.
Anthocyanins are more bioavailable than previously perceived, and their metabolites are present in the circulation for ≤48 h after ingestion. This trial was registered at clinicaltrials.gov as NCT01106729.
有证据表明,摄入富含花色苷的食物有益于心血管健康;然而,富含花色苷的食物的吸收、分布、代谢和消除(ADME)情况尚不清楚。
我们研究了人类对(13)C5 标记花色苷的 ADME。
8 名男性参与者摄入 500mg 同位素标记的矢车菊素-3-葡萄糖苷(6,8,10,3',5'-(13)C5-C3G)。在 48 小时内收集生物样本,并通过同位素比质谱和液相色谱-串联质谱法测量(13)C 和(13)C 标记代谢物的浓度。
尿液、呼气和粪便中(13)C 的回收率平均值±标准误为 43.9±25.9%(参与者之间的范围为 15.1-99.3%)。相对生物利用度为 12.38±1.38%(5.37±0.67%在尿液中排泄,6.91±1.59%在呼气中排泄)。摄入后 30 分钟达到(13)C 消除的最大速率(32.53±14.24μg(13)C/h),而(13)C 标记代谢物达到峰值(最大血清浓度:5.97±2.14μmol/L)在 10.25±4.14 h。(13)C 标记代谢物的半衰期在 12.44±4.22 到 51.62±22.55 h 之间。尿液中(13)C 的排泄在 0 到 1 小时之间最大(90.30±15.28μg/h),呼气中在 6 小时时最大(132.87±32.23μg/h),粪便中在 6 到 24 小时之间最大(557.28±247.88μg/h),而尿液(10.77±4.52μmol/L)和粪便样本(43.16±18.00μmol/L)中(13)C 标记代谢物的浓度在 6 到 24 小时之间最高。代谢物被鉴定为降解产物、酚类、马尿酸、苯乙酸和苯丙烯酸。
花色苷的生物利用度高于先前的认知,摄入后其代谢物在循环中存在≤48 小时。该试验在 clinicaltrials.gov 上注册为 NCT01106729。