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某些膳食生物活性化合物对人滋养层细胞系BeWo摄取叶酸及叶酸转运蛋白表达的急性和慢性影响。

Acute and chronic effects of some dietary bioactive compounds on folic acid uptake and on the expression of folic acid transporters by the human trophoblast cell line BeWo.

作者信息

Keating Elisa, Lemos Clara, Gonçalves Pedro, Martel Fátima

机构信息

Department of Biochemistry (U38-FCT), Faculty of Medicine, University of Porto, 4200-319 Porto, Portugal.

出版信息

J Nutr Biochem. 2008 Feb;19(2):91-100. doi: 10.1016/j.jnutbio.2007.01.007. Epub 2007 May 24.

Abstract

Folic acid (FA) is a vitamin that acts as a coenzyme in the biosynthesis of purine and pyrimidine precursors of nucleic acids, which are critically important during pregnancy. Our group has previously shown that both reduced folate carrier (RFC1) and folate receptor alpha (FRalpha) seem to be involved in the uptake of [3H]folic acid ([3H]FA) by a human trophoblast cell line (BeWo) and by human primary cultured cytotrophoblasts. Our aim was to study the interaction between FA and some nutrients/bioactive substances. For this, we tested the acute and chronic effects of some dietary compounds on [3H]FA apical uptake and on the expression of both RFC1 and FRalpha mRNA in BeWo cells. Our results show that [3H]FA uptake was significantly reduced by acute exposure to epicatechin, isoxanthohumol (1-400 microM) or theophylline (0.1-100 microM); isoxanthohumol seemed to act as a competitive inhibitor, whereas epicatechin and theophylline caused an increase in both Km and Vmax. On the other hand, [3H]FA uptake was significantly increased by chronic exposure to xanthohumol, quercetin or isoxanthohumol (0.1-10 microM), and this increase does not seem to result from changes in the level of RFC1 or FRalpha gene expression. Moreover, [3H]FA uptake was significantly reduced by chronic exposure to ethanol (0.01%). This reduction seems to be, at least in part, due to a reduction in FRalpha expression. These results are compatible with an association between a deficient FA supply to the placenta/fetus and ethanol toxicity in pregnancy.

摘要

叶酸(FA)是一种维生素,在核酸嘌呤和嘧啶前体的生物合成中作为辅酶,这在孕期至关重要。我们团队之前已经表明,还原型叶酸载体(RFC1)和叶酸受体α(FRα)似乎都参与了人滋养层细胞系(BeWo)和人原代培养的细胞滋养层细胞对[3H]叶酸([3H]FA)的摄取。我们的目的是研究叶酸与一些营养素/生物活性物质之间的相互作用。为此,我们测试了一些膳食化合物对[3H]FA顶端摄取以及BeWo细胞中RFC1和FRα mRNA表达的急性和慢性影响。我们的结果表明,急性暴露于表儿茶素、异黄腐醇(1 - 400 microM)或茶碱(0.1 - 100 microM)会显著降低[3H]FA的摄取;异黄腐醇似乎起竞争性抑制剂的作用,而表儿茶素和茶碱会导致Km和Vmax均增加。另一方面,长期暴露于黄腐醇、槲皮素或异黄腐醇(0.1 - 10 microM)会显著增加[3H]FA的摄取,并且这种增加似乎并非由RFC1或FRα基因表达水平的变化导致。此外,长期暴露于乙醇(0.01%)会显著降低[3H]FA的摄取。这种降低似乎至少部分是由于FRα表达的减少。这些结果与胎盘/胎儿叶酸供应不足与孕期乙醇毒性之间的关联相符。

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