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首页> 外文期刊>The American Journal of Clinical Nutrition: Official Journal of the American Society for Clinical Nutrition >Plasma kinetics of lutein, zeaxanthin, and 3-dehydro-lutein after multiple oral doses of a lutein supplement.
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Plasma kinetics of lutein, zeaxanthin, and 3-dehydro-lutein after multiple oral doses of a lutein supplement.

机译:在多次口服叶黄素补充剂后,叶黄素,玉米黄质和3-脱氢叶黄素的血浆动力学。

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BACKGROUND: Adequate intake of lutein is postulated to reduce the risk of age-related macular degeneration, but kinetic information for developing a dosing regimen is sparse. OBJECTIVE: The objective was to characterize lutein plasma kinetics in a multiple dosing design and to assess the effects of lutein intake on concentrations of other plasma carotenoids. DESIGN: After a run-in period of 7 d, 19 healthy volunteers were assigned to receive daily oral doses of 4.1 mg lutein (n = 8; group 1) or 20.5 mg lutein (n = 8; group 2) for 42 d or no lutein (n = 3; control group). The supplement contained 8.3% zeaxanthin relative to lutein (100%). The time profiles of plasma xanthophyll concentrations were monitored over the dosing phase, and samples were collected frequently on day 42 and for 24 d after dosing. RESULTS: Average plasma all-E-lutein concentrations increased from 0.14 to 0.52 +/- 0.13 and 1.45 +/- 0.69 mumol/L in groups 1 and 2, respectively. Dose-normalized lutein bioavailability in group 2 was approximately 60% of that in group 1. Kinetic disposition half-life did not differ significantly between groups. On average, dosing for 18 d was required to reach a >90% fraction of the steady state concentration, which is consistent with an effective half-life for accumulation of approximately 5.6 d. Plasma kinetics of all-E-lutein were paralleled by those of all-E-3-dehydro-lutein. Kinetic analysis indicated formation of all-E-3-dehydro-lutein from lutein. Lutein was well tolerated and did not affect the concentrations of other carotenoids. CONCLUSION: Long-term supplementation with 4.1 and 20.5 mg lutein as beadlets increased plasma lutein concentrations approximately 3.5- and 10-fold, respectively.
机译:背景:叶黄素的摄入被认为可以减少与年龄相关的黄斑变性的风险,但是制定剂量方案的动力学信息很少。目的:目的是通过多次给药设计表征叶黄素血浆动力学,并评估叶黄素摄入对其他血浆类胡萝卜素浓度的影响。设计:经过7天的磨合期,分配了19名健康志愿者接受42 d或每天口服剂量的4.1 mg叶黄素(n = 8;第1组)或20.5 mg叶黄素(n = 8;第2组)。没有叶黄素(n = 3;对照组)。该补充剂相对于叶黄素(100%)含有8.3%的玉米黄质。在给药阶段监测血浆叶黄素浓度的时间曲线,并在给药后第42天和给药后24 d频繁收集样品。结果:第1组和第2组的血浆全E叶黄素平均浓度分别从0.14和0.52 +/- 0.13和1.45 +/- 0.69 mumol / L增加。第2组的剂量标准化叶黄素生物利用度约为第1组的60%。动力学处置半衰期在各组之间无显着差异。平均而言,需要给药18天才能达到稳态浓度的> 90%,这与累积约5.6天的有效半衰期相符。全E-叶黄素的血浆动力学与全E-3-脱氢叶黄素的血浆动力学平行。动力学分析表明由叶黄素形成全E-3-脱氢叶黄素。叶黄素耐受性好,不影响其他类胡萝卜素的浓度。结论:长期补充4.1和20.5 mg叶黄素作为小球,可使血浆叶黄素浓度分别增加约3.5倍和10倍。

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