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肠道磷吸收:转化和临床研究中的新发现。

Intestinal phosphorus absorption: recent findings in translational and clinical research.

机构信息

Department of Food Science and Nutrition, University of Minnesota, St. Paul, Minnesota.

Department of Medicine/Division of Nephrology, Indiana University School of Medicine, Indianapolis.

出版信息

Curr Opin Nephrol Hypertens. 2021 Jul 1;30(4):404-410. doi: 10.1097/MNH.0000000000000719.

Abstract

PURPOSE OF REVIEW

The purpose of this review is to discuss recent findings in intestinal phosphorus absorption pathways, particularly the contributions of paracellular versus transcellular absorption, and the differential findings from studies using in vitro versus in vivo techniques of assessing phosphorus absorption in experimental animal studies.

RECENT FINDINGS

Experimental animal studies show that in vivo effects of low phosphorus diets, 1,25D, and chronic kidney disease on intestinal phosphorus absorption efficiency contradict effects previously established ex vivo/in vitro. Recent in vivo studies also suggest that the paracellular pathway accounts for the majority of phosphorus absorption in animals across very low to high luminal phosphate concentrations. The data from experimental animal studies correspond to recent human studies showing the effectiveness of targeted inhibition of paracellular phosphate absorption. Additionally, recent human studies have demonstrated that NaPi-2b inhibition alone does not appear to be effective in lowering serum phosphate levels in patients with chronic kidney disease. Pursuit of other transcellular phosphate transporter inhibitors may still hold promise.

SUMMARY

In vivo animal and human studies have added to our understanding of intestinal phosphorus absorption pathways, regulation, and mechanisms. This is beneficial for developing effective new strategies for phosphate management in patients with chronic kidney disease.

摘要

目的综述

本文旨在讨论肠道磷吸收途径的最新研究结果,特别是细胞旁途径与细胞内途径吸收的作用,以及采用评估实验动物磷吸收的体内与体外技术的研究在磷吸收方面得出的不同发现。

最近的发现

实验动物研究表明,低磷饮食、1,25D 和慢性肾脏病对肠道磷吸收效率的体内影响与之前在体外用/in vitro 技术建立的作用相悖。最近的体内研究还表明,在非常低到高肠腔磷酸盐浓度范围内,细胞旁途径是动物磷吸收的主要途径。这些来自实验动物研究的数据与最近的人类研究结果一致,表明靶向抑制细胞旁磷酸盐吸收在降低慢性肾脏病患者血清磷酸盐水平方面是有效的。此外,最近的人类研究表明,单独抑制 NaPi-2b 似乎并不能有效降低慢性肾脏病患者的血清磷酸盐水平。寻求其他细胞内磷酸盐转运体抑制剂可能仍然有希望。

总结

体内动物和人体研究增加了我们对肠道磷吸收途径、调节和机制的理解。这有利于为慢性肾脏病患者开发有效的磷酸盐管理新策略。

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本文引用的文献

1
Intestinal Phosphorus Absorption in Moderate CKD and Healthy Adults Determined Using a Radioisotopic Tracer.
J Am Soc Nephrol. 2021 Aug;32(8):2057-2069. doi: 10.1681/ASN.2020091340. Epub 2021 Jul 8.
2
Targeting NaPi-IIb for Hyperphosphatemia in Chronic Kidney Disease Patients - The Dead End?
Kidney Int Rep. 2021 Feb 3;6(3):557-558. doi: 10.1016/j.ekir.2021.01.017. eCollection 2021 Mar.
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NaPi-IIb Inhibition for Hyperphosphatemia in CKD Hemodialysis Patients.
Kidney Int Rep. 2020 Dec 23;6(3):675-684. doi: 10.1016/j.ekir.2020.12.017. eCollection 2021 Mar.
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Increased intestinal phosphate absorption, an often-overlooked effect of vitamin D.
J Physiol. 2021 Feb;599(4):1021-1022. doi: 10.1113/JP281095. Epub 2020 Dec 18.
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Combination treatment with tenapanor and sevelamer synergistically reduces urinary phosphorus excretion in rats.
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Importance of Dietary Phosphorus for Bone Metabolism and Healthy Aging.
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