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肠道叶酸吸收。I. 5-甲基四氢叶酸。

Intestinal folate absorption. I. 5-Methyltetrahydrofolic acid.

作者信息

Strum W, Nixon P F, Bertino J B, Binder H J

出版信息

J Clin Invest. 1971 Sep;50(9):1910-6. doi: 10.1172/JCI106683.

Abstract

Intestinal absorption of the monoglutamate form of the principal dietary and circulating folate compound, 5-methyltetrahydrofolic acid (5-MTHF), was studied in the rat utilizing a synthetic highly purified radiolabeled diastereoisomer. Chromatography confirmed that the compound was not altered after transfer from the mucosa to the serosa. Accumulation against a concentration gradient was not observed in duodenal, jejunal, or ileal segments at 5-MTHF concentration from 0.5 to 500 nmoles/liter. Unidirectional transmural flux determination also did not indicate a significant net flux. Mucosal to serosal transfer of 5-MTHF was similar in all segments of the intestine and increased in a linear fashion with increased initial mucosal concentrations. Further, no alteration in 5-MTHF transfer was found when studied in the presence of metabolic inhibitors or folate compounds. These results indicate that 5-MTHF is not absorbed by the rat small intestine by a carrier-mediated system and suggest that 5-MTHF transfer most likely represents diffusion.

摘要

利用一种合成的高度纯化的放射性标记非对映异构体,在大鼠中研究了主要膳食和循环叶酸化合物单谷氨酸形式的5-甲基四氢叶酸(5-MTHF)的肠道吸收情况。色谱分析证实,该化合物从黏膜转移至浆膜后未发生改变。在5-MTHF浓度为0.5至500纳摩尔/升时,十二指肠、空肠或回肠段均未观察到逆浓度梯度的积累。单向跨壁通量测定也未显示出明显的净通量。5-MTHF从黏膜到浆膜的转移在肠道的所有段中相似,并且随着初始黏膜浓度的增加呈线性增加。此外,在存在代谢抑制剂或叶酸化合物的情况下进行研究时,未发现5-MTHF转移有任何改变。这些结果表明,5-MTHF不是通过载体介导的系统被大鼠小肠吸收的,提示5-MTHF的转移很可能代表扩散。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5ca/292117/3348a5820847/jcinvest00197-0143-a.jpg

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