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补充L-苯丙氨酸和高蛋白饮食对健康志愿者中头孢地尼药代动力学的影响:一项探索性研究。

Effect of L-phenylalanine supplementation and a high-protein diet on pharmacokinetics of cefdinir in healthy volunteers: an exploratory study.

作者信息

Fujita T, Nakamura K, Yamazaki A, Ozaki M, Sahashi K, Shichijo K, Nomura K, Maeda M, Nakamura T, Fujita T, Yokota S, Kuroyama S, Kumagai Y, Majima M, Ohtani Y

机构信息

Department of Pharmacology, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.

出版信息

J Clin Pharm Ther. 2007 Jun;32(3):277-85. doi: 10.1111/j.1365-2710.2007.00826.x.

DOI:10.1111/j.1365-2710.2007.00826.x
PMID:17489880
Abstract

BACKGROUND

Upregulation of oligopeptide transport activity by dietary protein, certain dipeptides and amino acids has been reported in the rat intestine and a human intestinal cell line.

OBJECTIVE

In this study, the pharmacokinetics of cefdinir were investigated after L-phenylalanine supplementation and a high-protein diet (HPD) in humans to explore changes in the activities of intestinal and renal oligopeptide transporters.

METHODS

A normal-protein diet (NPD, 73.2 +/- 2.6 g/day), NPD + l-phenylalanine (7.5 g/day), or HPD (141.3 +/- 3.7 g/day) was given to six male healthy volunteers for 12 days followed by a single dose of cefdinir after an overnight fast in a randomized three-way crossover study with a 22-day washout. Blood and urine were collected over a 12-h period after administration of cefdinir. Concentrations of cefdinir in plasma and/or urine were measured by high-performance liquid chromatography.

RESULTS

Plasma concentrations and urinary excretion of the drug did not change throughout the study. Physiological variables and laboratory values did not reveal any differences between the three periods except for serum and urinary nitrogen levels and serum triglyceride.

DISCUSSION

A reason for the unchanged pharmacokinetics of cefdinir may be due to lower doses of L-phenylalanine and protein in humans than in animals when converting animal effective doses to humans.

CONCLUSION

In humans, L-phenylalanine supplementation and HPD do not seem to upregulate intestinal and renal oligopeptide transport in the ranges of duration and dose examined.

摘要

背景

据报道,大鼠肠道和人肠道细胞系中,膳食蛋白质、某些二肽和氨基酸可上调寡肽转运活性。

目的

本研究通过补充L-苯丙氨酸和给予高蛋白饮食(HPD),研究头孢地尼在人体内的药代动力学,以探讨肠道和肾脏寡肽转运体活性的变化。

方法

在一项随机三交叉研究中,6名健康男性志愿者接受正常蛋白饮食(NPD,73.2±2.6克/天)、NPD+L-苯丙氨酸(7.5克/天)或HPD(141.3±3.7克/天)12天,随后在禁食过夜后单次服用头孢地尼,洗脱期为22天。服用头孢地尼后12小时内收集血液和尿液。采用高效液相色谱法测定血浆和/或尿液中头孢地尼的浓度。

结果

在整个研究过程中,药物的血浆浓度和尿排泄量没有变化。除血清和尿氮水平以及血清甘油三酯外,生理变量和实验室值在三个时期之间未显示出任何差异。

讨论

头孢地尼药代动力学未改变的一个原因可能是,在将动物有效剂量换算为人体剂量时,人体中L-苯丙氨酸和蛋白质的剂量低于动物。

结论

在本研究的持续时间和剂量范围内,补充L-苯丙氨酸和HPD似乎不会上调人体肠道和肾脏的寡肽转运。

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