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盐酸吡哆醇在大鼠空肠中的体内吸收与磷酸化作用

In vivo absorption and phosphorylation of pyridoxine . HCl in rat jejunum.

作者信息

Middleton H M

出版信息

Gastroenterology. 1979 Jan;76(1):43-9.

PMID:758146
Abstract

The absorption and phosphorylation of 3H-pyridoxine . HCl were studied in vivo in isolated loops of rat jejunum. Uptake was rapid and linear over the concentration range of 0.2-1 mM; tissue content of absorbed vitamin was saturable and consisted primarily of phosphorylated forms of vitamin B6. Phosphorylation was saturable with a Km of 11.6 micronM and a Vmax of 1.65 nmol/5 min/g wet tissue. Inhibition of phosphorylation changed neither the t 1/2 of 3H-pyridoxine . HCl disappearance from the lumen nor the calculated uptake after either 5-min or 30-min absorption periods. Inhibition of phosphorylation, however, significantly decreased the t 1/2 for transmural absorption and significantly increased the calculated transmural absorption after a 5-min absorption period. These studies indicate that (a) pyridoxine absorption, over the concentration range tested, is nonsaturable and consistent with passive diffusion; (b) jejunal phosphorylation of pyridoxine occurs in vivo, is saturable, and results in saturation of tissue content of the absorbed vitamin; and (c) phosphorylation has no significant effect on the uptake of pyridoxine but significantly delays the transmural absorption of a finite amount of the vitamin.

摘要

在大鼠空肠分离肠袢中对3H - 盐酸吡哆醇的吸收和磷酸化进行了体内研究。在0.2 - 1 mM的浓度范围内,摄取迅速且呈线性;吸收的维生素的组织含量是可饱和的,主要由维生素B6的磷酸化形式组成。磷酸化是可饱和的,Km为11.6微摩尔,Vmax为1.65纳摩尔/5分钟/克湿组织。磷酸化的抑制既不改变3H - 盐酸吡哆醇从肠腔消失的t1/2,也不改变5分钟或30分钟吸收期后的计算摄取量。然而,磷酸化的抑制显著降低了跨壁吸收的t1/2,并显著增加了5分钟吸收期后的计算跨壁吸收量。这些研究表明:(a)在所测试的浓度范围内,吡哆醇的吸收是不饱和的,与被动扩散一致;(b)空肠中吡哆醇的磷酸化在体内发生,是可饱和的,并导致吸收的维生素的组织含量饱和;(c)磷酸化对吡哆醇的摄取没有显著影响,但显著延迟了有限量维生素的跨壁吸收。

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