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吡哆醇-5'-β-D-葡萄糖苷影响大鼠体内吡哆醇的短期代谢利用。

Pyridoxine-5'-beta-D-glucoside influences the short-term metabolic utilization of pyridoxine in rats.

作者信息

Nakano H, Gregory J F

机构信息

Food Science and Human Nutrition Department, University of Florida, Gainesville 32611-0370, USA.

出版信息

J Nutr. 1995 Apr;125(4):926-32. doi: 10.1093/jn/125.4.926.

Abstract

This study was conducted to characterize the initial time course of the apparent competitive effect of pyridoxine-5'-beta-D-glucoside against co-ingested pyridoxine. Two groups of rats were administered a single oral dose of 100 nmol of [14C]pyridoxine along with either 0 or 20 nmol of unlabeled pyridoxine-5'-beta-D-glucoside. At 6, 12, 24 and 48 h post-dose, the distribution of labeled vitamin B-6 metabolites in blood, tissues and urine was determined. Urinary [14C]4-pyridoxic acid comprised a significantly greater percentage of excreted 14C in the control group, with the greatest difference at 12 h post-dose. Pyridoxine-5'-beta-D-glucoside (10-15 nmol) was excreted mainly in unchanged form within 6 h. Rats that received pyridoxine-5'-beta-D-glucoside retained less 14C in liver, with a maximal difference between groups at 6-12 h post-dose. The relative concentrations of hepatic [14C]pyridoxal 5'-phosphate and [14C]pyridoxamine 5'-phosphate in the treatment group were greater than in the control group at approximately 12 h post-dose. At 48 h post-dose, there was no difference in the distribution of any vitamin B-6 metabolite except pyridoxal 5'-phosphate in the two groups. These results confirm that a small, nutritionally relevant dose of pyridoxine-5'-beta-D-glucoside influences the utilization of pyridoxine and indicate that this is a short-term, transient effect.

摘要

本研究旨在描述吡哆醇-5'-β-D-葡萄糖苷对同时摄入的吡哆醇的表观竞争效应的初始时间进程。将两组大鼠口服给予单剂量100 nmol的[14C]吡哆醇,同时分别给予0或20 nmol未标记的吡哆醇-5'-β-D-葡萄糖苷。给药后6、12、24和48小时,测定血液、组织和尿液中标记的维生素B-6代谢物的分布。在对照组中,尿中[14C]4-吡哆酸占排泄的14C的百分比显著更高,给药后12小时差异最大。吡哆醇-5'-β-D-葡萄糖苷(10 - 15 nmol)在6小时内主要以未改变的形式排泄。接受吡哆醇-5'-β-D-葡萄糖苷的大鼠肝脏中保留的14C较少,给药后6 - 12小时两组间差异最大。给药后约12小时,治疗组肝脏中[14C]吡哆醛5'-磷酸和[14C]吡哆胺5'-磷酸的相对浓度高于对照组。给药后48小时,除吡哆醛5'-磷酸外,两组中任何维生素B-6代谢物的分布均无差异。这些结果证实,少量与营养相关剂量的吡哆醇-5'-β-D-葡萄糖苷会影响吡哆醇的利用,并表明这是一种短期的、短暂的效应。

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