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首页> 外文期刊>Journal of Nutritional Science and Vitaminology >Vitamin C Activity of Dehydroascorbic Acid in Humans —Association between Changes in the Blood Vitamin C Concentration or Urinary Excretion after Oral Loading—
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Vitamin C Activity of Dehydroascorbic Acid in Humans —Association between Changes in the Blood Vitamin C Concentration or Urinary Excretion after Oral Loading—

机译:人体中脱氢抗坏血酸的维生素C活性—口服负荷后血液中维生素C浓度变化或尿液排泄之间的关系—

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We performed oral loading of AsA or DAsA (1 mmol) in subjects who had consumed a diet low in vitamin C (C) (C≤5 mg/d) for 3 d before loading, and measured urinary and blood vitamin C. Since the crossover method was used, the same experiment was repeated after an interval of about 1 mo in each subject. The results of the experiment including a total of 17 subjects for 2005 and 2006, were as follows. (1) There were marked individual differences in urinary C excretion. (2) The C level in 24-h urine after C loading did not differ between the two orally administered C forms (AsA and DAsA). (3) C excretion between 0 and 3 h after C loading was significantly higher ( p <0.05) for the DAsA group, while those between 3 and 6, 6 and 9, 9 and 12, and 12 and 24 h after C loading were significantly higher ( p <0.05 or p <0.01) for the AsA group. (4) The blood C concentration and the increase in C 1 h after C loading were significantly higher ( p <0.05 and p <0.01, respectively) in the DAsA than in the AsA group. (5) Evaluation of the association between C metabolism and the single nucleotide polymorphisms of glutathione S -transferase P (GSTP) 1-1 showed a lower urinary C excretion and a significantly lower C level in 24-h urine ( p <0.05) after AsA loading, and a significantly lower urinary C excretion between 0 and 3 h after DAsA loading ( p <0.05) for the GA heterozygotes than for the AA homozygotes. Considering the activity of C as DAsA in humans, based on urinary and blood C levels after a single loading of C, the utilization of DAsA is equivalent to that of AsA, although the metabolic turnover time is different. The involvement of polymorphisms in the xenobiotic metabolizing enzyme, GSTP1-1, in C metabolism, particularly urinary C excretion, was also clarified. This demonstrates the necessity of considering gene polymorphisms in determining individual C requirements. An abstract of this paper was reported by the Vitamin C Research Committee (Ochanomizu University) in 2007.
机译:我们对摄入维生素C(C)(C≤5mg / d)低饮食的受试者连续3 d口服AsA或DAsA(1 mmol),并测定了尿和血液中的维生素C。使用交叉法,每个受试者间隔约1个月后重复相同的实验。该实验的结果包括2005年和2006年的17个主题。 (1)尿C排泄存在明显的个体差异。 (2)两种口服C形式(AsA和DAsA)在加载C后24小时尿液中的C水平没有差异。 (3)DAsA组C负荷后0至3 h的C排泄显着更高(p <0.05),而Cs负荷后3至6、6与9、9和12以及12至24 h的C排泄则较高。 AsA组明显更高(p <0.05或p <0.01)。 (4)DAsA组的血液中C浓度和C负荷后1 h C的增加显着高于AsA组(分别为p <0.05和p <0.01)。 (5)评价C代谢与谷胱甘肽S-转移酶P(GSTP)1-1的单核苷酸多态性之间的关联后,尿24小时后尿C排泄量降低,C水平显着降低(p <0.05)与AA纯合子相比,GA杂合子的AsA加载量和DAsA加载后0到3小时之间的尿C排泄量显着降低(p <0.05)。考虑到人类中C作为DAsA的活性,基于单次加载C后尿液和血液中C的水平,尽管代谢转换时间不同,但DAsA的利用与AsA相同。还明确了异源代谢酶GSTP1-1中的多态性与碳代谢特别是尿液C的排泄有关。这表明在确定单个C需求时考虑基因多态性的必要性。维生素C研究委员会(御茶水大学)于2007年报道了该论文的摘要。

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