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叶黄素酯强化发酵乳中游离叶黄素的生物利用度:体内和体外研究。

Lutein bioavailability from lutein ester-fortified fermented milk: in vivo and in vitro study.

机构信息

Unidad de Vitaminas, Servicio de Bioquímica Clínica, Hospital Universitario Puerta de Hierro, 28035-Madrid, Spain.

出版信息

J Nutr Biochem. 2010 Feb;21(2):133-9. doi: 10.1016/j.jnutbio.2008.12.002. Epub 2009 Feb 6.

Abstract

We assessed the bioavailability of lutein from lutein-fortified fermented milk using in vivo and in vitro approaches. Twenty-four volunteers were randomized to take lutein-fortified fermented milk at two levels of fortification. Single-dose bioavailability study (2x100 ml, ca. 8 or 16 mg of lutein) was performed using a three-point approach (baseline, 3.5 and 6.5 h). Multiple-dose study consisted of consuming one serving/day (ca. 4 or 8 mg/100 ml) for 14 days. Blood samples for biochemical, hematological and lutein analysis were drawn at baseline, Day 7 and Day 14. In vitro bioaccessibility was assessed by a static gastrointestinal digestion model. Lutein content, in vitro ester hydrolysis and micellarization, and lutein concentrations achieved in serum were analyzed by HPLC. In vivo, post-prandial response was higher using the high content fermented milk, but the percentage of absorption was not different according to the dose consumed. Net increments at Day 7 and Day 14 were significantly higher on consuming the high-dose milk as well. In vitro, lutein ester hydrolysis was incomplete regardless of the amount initially present. Free lutein released was higher using the high-dose fermented milk, but the percentage of hydrolysis was similar at both levels of fortification. In the micellar phase, the percentage of free and total lutein was not different according to the dose. Our results support the suitability of the fermented milk as a carrier of lutein esters and an in vivo dose-dependent effect upon regular consumption and suggest the usefulness of in vitro models to provide relevant information to predict in vivo responses.

摘要

我们采用体内和体外方法评估了强化发酵乳中叶黄素的生物利用度。24 名志愿者随机分为两组,分别服用两种强化水平的强化发酵乳。采用三点法(基线、3.5 和 6.5 h)进行单次剂量生物利用度研究(2x100 ml,约 8 或 16 mg 叶黄素)。多次剂量研究包括每天服用一份(约 4 或 8 mg/100 ml),持续 14 天。在基线、第 7 天和第 14 天采集用于生化、血液学和叶黄素分析的血样。通过静态胃肠道消化模型评估叶黄素的体外生物可及性。通过 HPLC 分析叶黄素含量、体外酯水解和胶束化以及血清中达到的叶黄素浓度。在体内,高含量发酵乳的餐后反应更高,但根据消耗的剂量,吸收率没有差异。第 7 天和第 14 天的净增量在高剂量牛奶的消耗中明显更高。体外,无论最初存在的量如何,叶黄素酯的水解都不完全。使用高剂量发酵乳释放的游离叶黄素更高,但两种强化水平的水解率相似。在胶束相中,根据剂量,游离和总叶黄素的百分比没有差异。我们的结果支持发酵乳作为叶黄素酯载体的适宜性,以及在常规消费时的体内剂量依赖性效应,并表明体外模型可用于提供相关信息来预测体内反应的有用性。

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