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新型铁-乳清蛋白微球可保护肠道上皮细胞免受铁相关氧化应激和损伤,并改善空腹成年人的铁吸收。

Novel Iron-Whey Protein Microspheres Protect Gut Epithelial Cells from Iron-Related Oxidative Stress and Damage and Improve Iron Absorption in Fasting Adults.

作者信息

Wang Jun, Radics Gabor, Whelehan Michael, OʼDriscoll Aoibhe, Healy Anne Marie, Gilmer John F, Ledwidge Mark

机构信息

School of Pharmacy and Pharmaceutical Sciences, Trinity College Dublin, Dublin, Ireland.

出版信息

Acta Haematol. 2017;138(4):223-232. doi: 10.1159/000480632. Epub 2018 Jan 5.

Abstract

BACKGROUND

Iron food fortification and oral iron formulations are frequently limited by poor absorption, resulting in the widespread use of high-dose oral iron, which is poorly tolerated.

METHODS

We evaluated novel iron-denatured whey protein (Iron-WP) microspheres on reactive oxygen species (ROS) and viability in gut epithelial (HT29) cells. We compared iron absorption from Iron-WP versus equimolar-dose (25 mg elemental iron) ferrous sulphate (FeSO4) in a prospective, randomised, cross-over study in fasting volunteers (n = 21 per group) dependent on relative iron depletion (a ferritin level ≤/>30 ng/mL).

RESULTS

Iron-WP caused less ROS generation and better HT29 cell viability than equimolar FeSO4. Iron-WP also showed better absorption with a maximal 149 ± 39% increase in serum iron compared to 65 ± 14% for FeSO4 (p = 0.01). The response to both treatments was dependent on relative iron depletion, and multi-variable analysis showed that better absorption with Iron-WP was independent of baseline serum iron, ferritin, transferrin saturation, and haemoglobin in the overall group and in the sub-cohort with relative iron depletion at baseline (p < 0.01).

CONCLUSIONS

Novel Iron-WP microspheres may protect gut epithelial cells and improve the absorption of iron versus FeSO4. Further evaluation of this approach to food fortification and supplementation with iron is warranted.

摘要

背景

铁强化食品和口服铁制剂常常因吸收不佳而受到限制,导致高剂量口服铁的广泛使用,但其耐受性较差。

方法

我们评估了新型铁变性乳清蛋白(Iron-WP)微球对肠道上皮(HT29)细胞中活性氧(ROS)和细胞活力的影响。在一项前瞻性、随机、交叉研究中,我们比较了Iron-WP与等摩尔剂量(25毫克元素铁)硫酸亚铁(FeSO4)在空腹志愿者(每组n = 21)中的铁吸收情况,这些志愿者依赖于相对铁缺乏(铁蛋白水平≤/>30纳克/毫升)。

结果

与等摩尔的FeSO4相比,Iron-WP产生的ROS更少,HT29细胞活力更好。Iron-WP的吸收也更好,血清铁最大增加149±39%,而FeSO4为65±14%(p = 0.01)。两种治疗的反应均取决于相对铁缺乏,多变量分析表明,在整个组以及基线时相对铁缺乏的亚组中,Iron-WP更好的吸收与基线血清铁、铁蛋白、转铁蛋白饱和度和血红蛋白无关(p < 0.01)。

结论

新型Iron-WP微球可能保护肠道上皮细胞,并比FeSO4提高铁的吸收。有必要对这种食品强化和铁补充方法进行进一步评估。

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