Suppr超能文献

在动态体外胃肠模型中测定发现,强化牛奶中的叶酸和5-甲基四氢叶酸具有生物可及性。

Folic acid and 5-methyltetrahydrofolate in fortified milk are bioaccessible as determined in a dynamic in vitro gastrointestinal model.

作者信息

Verwei Miriam, Arkbåge Karin, Havenaar Robert, van den Berg Henk, Witthöft Cornelia, Schaafsma Gertjan

机构信息

TNO-WU Center for Micronutrient Research, 3700 AJ Zeist, The Netherlands.

出版信息

J Nutr. 2003 Jul;133(7):2377-83. doi: 10.1093/jn/133.7.2377.

Abstract

Dairy products are a potential matrix for folate fortification to enhance folate consumption in the Western world. Milk folate-binding proteins (FBP) are especially interesting because they seem to be involved in folate bioavailability. In this study, folate bioaccessibility was investigated using a dynamic computer-controlled gastrointestinal model [TNO gastrointestinal model (TIM)]. We used both ultrahigh temperature (UHT)-processed milk and pasteurized milk, differing in endogenous FBP concentrations and fortified with folic acid or 5-methyltetrahydrofolate (5-CH(3)-H(4)folate). To study FBP stability during gastrointestinal passage and the effect of additional FBP on folate bioaccessibility, FBP-fortified UHT and pasteurized milk products were also tested. Folate bioaccessibility and FBP stability were measured by taking samples along the compartments of the gastrointestinal model and measuring their folate and FBP concentrations. Folate bioaccessibility from folic acid-fortified milk products without additional FBP was 58-61%. This was lower (P < 0.05) than that of the 5-CH(3)-H(4)folate-fortified milk products (71%). Addition of FBP reduced (P < 0.05) folate bioaccessibility from folic acid-fortified milk (44-51%) but not from 5-CH(3)-H(4)folate-fortified milk products (72%). The residual FBP levels in the folic acid- and 5-CH(3)-H(4)folate-fortified milk products after gastrointestinal passage were 13-16% and 0-1%, respectively, of the starting amounts subjected to TIM. In conclusion, milk seems to be a suitable carrier for folate, because both folic acid and 5-CH(3)-H(4)folate are easily released from the matrix and available for absorption. However, our results suggest that folic acid remains partly bound to FBP during passage through the small intestine, which reduces the bioaccessibility of folic acid from milk in this model.

摘要

乳制品是西方世界强化叶酸以增加叶酸摄入量的潜在载体。牛奶中的叶酸结合蛋白(FBP)尤其值得关注,因为它们似乎与叶酸的生物利用度有关。在本研究中,使用动态计算机控制的胃肠道模型[TNO胃肠道模型(TIM)]研究了叶酸的生物可及性。我们使用了超高温(UHT)处理的牛奶和巴氏杀菌牛奶,它们的内源性FBP浓度不同,并添加了叶酸或5-甲基四氢叶酸(5-CH(3)-H(4)folate)。为了研究胃肠道通过过程中FBP的稳定性以及额外FBP对叶酸生物可及性的影响,还测试了添加FBP的UHT和巴氏杀菌牛奶产品。通过在胃肠道模型的各个隔室中取样并测量其叶酸和FBP浓度来测定叶酸生物可及性和FBP稳定性。未添加额外FBP的叶酸强化牛奶产品的叶酸生物可及性为58 - 61%。这低于(P < 0.05)5-CH(3)-H(4)folate强化牛奶产品(71%)的生物可及性。添加FBP降低了(P < 0.05)叶酸强化牛奶的叶酸生物可及性(44 - 51%),但对5-CH(3)-H(4)folate强化牛奶产品没有影响(72%)。经过胃肠道通过后,叶酸和5-CH(3)-H(4)folate强化牛奶产品中残留的FBP水平分别为TIM起始量的13 - 16%和0 - 1%。总之,牛奶似乎是叶酸的合适载体,因为叶酸和5-CH(3)-H(4)folate都能轻易从基质中释放出来并可供吸收。然而,我们的结果表明,在通过小肠的过程中,叶酸仍有部分与FBP结合,这降低了该模型中牛奶中叶酸的生物可及性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验