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Acid hydrolysis of jaboticaba ( Myrciaria jaboticaba ) peel and seed powder increases urolithin excretion in a cross-over clinical trial with normoweight subjects

生物利用度 化学 新陈代谢 食品科学 水解 排泄 临床试验 生物化学 多酚 膳食补充剂 健康福利 药理学 人类健康 植物代谢 药代动力学 羟基酪醇
作者
Rafael Bizarelo,Kim Ohanna Pimenta Inada,Daniel Perrone,Mariana Monteiro
出处
期刊:Food & Function [Royal Society of Chemistry]
卷期号:17 (9): 3986-3995
标识
DOI:10.1039/d5fo04952k
摘要

), and exhibit beneficial health effects primarily through urolithins, their gut-derived metabolites. However, the bioavailability and metabolism of ellagitannins are limited by their structural complexity and strong binding to the food matrix, which may attenuate their biological activity. Therefore, this study evaluated the impact of acid hydrolysis of jaboticaba peel and seeds on ellagitannin metabolism in normoweight subjects. In a randomized cross-over clinical trial, 23 subjects consumed capsules containing either 3 g of non-hydrolyzed jaboticaba peel and seed powder (JPSP) or 3 g of hydrolyzed jaboticaba peel and seed powder (HJPSP), separated by a 14-day washout period. Urine samples were collected at different intervals up to 72 h post-intake. The HJPSP intervention provided a 3.2-fold higher dose of free ellagic acid compared to JPSP (57.1 mg and 17.8 mg, respectively). On average, glucuronidated urolithins accounted for 85% of the total excreted amount. Urolithin A 3/8-glucuronide was the main metabolite, comprising 54% (JPSP) and 57% (HJPSP) of total urolithin excretion over 72 h. Although urolithins were only detected in urine samples 8 h after the intake of HJPSP, the time to maximal urolithin excretion did not differ between interventions (29.2 h for JPSP and 28.3 h for HJPSP). Finally, acid hydrolysis increased total urolithin excretion by up to 69% over 0-48 h after HJPSP intake compared to JPSP, with a 50% increase in total excretion over 72 h of urine collection. In conclusion, acid hydrolysis of jaboticaba peel and seeds enhances the production of urolithins in normoweight subjects, probably by increasing the availability of ellagic acid and low-polymerization ellagitannins for gut microbial conversion.
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