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SLC19A3 介导的吡哆醇转运功能在动物物种间的差异:大鼠小肠中不存在 Slc19a3 介导的吡哆醇摄取。

Animal species differences in the pyridoxine transport function of SLC19A3: Absence of Slc19a3-mediated pyridoxine uptake in the rat small intestine.

机构信息

Department of Biopharmaceutics, Graduate School of Pharmaceutical Sciences, Nagoya City University, 3-1 Tanabe-dori, Mizuho-ku, Nagoya, 467-8603, Japan.

Department of Biopharmaceutics, Graduate School of Pharmaceutical Sciences, Nagoya City University, 3-1 Tanabe-dori, Mizuho-ku, Nagoya, 467-8603, Japan.

出版信息

Drug Metab Pharmacokinet. 2022 Jun;44:100456. doi: 10.1016/j.dmpk.2022.100456. Epub 2022 Mar 9.

Abstract

The thiamine transporters, SLC19A2 and SLC19A3, have recently been shown to transport pyridoxine in addition to thiamine, the originally identified substrate, in our study on human orthologs. Based on these results, we characterized the rat and mouse orthologs for pyridoxine transport function. Through the assessment of pyridoxine uptake in human embryonic kidney 293 cells transiently expressing the SLC19A2/3 orthologs, we found that both rat and mouse Slc19a2 can transport pyridoxine, but rat or mouse Slc19a3 cannot. However, all SLC19A2/3 orthologs were capable of thiamine transport. We subsequently demonstrated in the rat small intestine that a carrier-mediated mechanism exists for thiamine uptake, but not for pyridoxine uptake. This is supported by the finding that rat Slc19a3, for which the human ortholog operates for the intestinal uptake of both pyridoxine and thiamine, lacks the pyridoxine transport function. Thus, SLC19A3s from different animal species exhibit differences in pyridoxine transport. Rats and mice, in which Slc19a3 lacks this function, are not suitable model animals for studies involving pyridoxine disposition and related issues.

摘要

我们的研究表明,除了最初确定的底物硫胺素外,硫胺素转运蛋白 SLC19A2 和 SLC19A3 还能转运吡哆醇。基于这些结果,我们对大鼠和小鼠的吡哆醇转运功能的同源物进行了表征。通过评估人胚肾 293 细胞中瞬时表达 SLC19A2/3 同源物的吡哆醇摄取情况,我们发现大鼠和小鼠 Slc19a2 都能转运吡哆醇,但大鼠或小鼠 Slc19a3 不能。然而,所有 SLC19A2/3 同源物都能转运硫胺素。随后,我们在大鼠小肠中证明了一种存在载体介导的机制来摄取硫胺素,但不存在摄取吡哆醇的机制。这一发现得到了支持,即大鼠 Slc19a3 的人类同源物负责肠道摄取吡哆醇和硫胺素,但缺乏吡哆醇的转运功能。因此,不同动物物种的 SLC19A3 表现出在吡哆醇转运方面的差异。缺乏这种功能的大鼠和小鼠不适合用于研究吡哆醇处置和相关问题。

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