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维生素 D、甲状旁腺激素(PTH)和磷酸盐(Pi)对磷酸盐的生理调节。

Physiological regulation of phosphate by vitamin D, parathyroid hormone (PTH) and phosphate (Pi).

机构信息

Centre for Nephrology, University College London (UCL), Royal Free Campus, Rowland Hill Street, London, NW3 2PF, UK.

AstraZeneca IMED ECD CVRM R&D, Gothenburg, Sweden.

出版信息

Pflugers Arch. 2019 Jan;471(1):83-98. doi: 10.1007/s00424-018-2231-z. Epub 2018 Nov 5.

Abstract

Inorganic phosphate (Pi) is an abundant element in the body and is essential for a wide variety of key biological processes. It plays an essential role in cellular energy metabolism and cell signalling, e.g. adenosine and guanosine triphosphates (ATP, GTP), and in the composition of phospholipid membranes and bone, and is an integral part of DNA and RNA. It is an important buffer in blood and urine and contributes to normal acid-base balance. Given its widespread role in almost every molecular and cellular function, changes in serum Pi levels and balance can have important and untoward effects. Pi homoeostasis is maintained by a counterbalance between dietary Pi absorption by the gut, mobilisation from bone and renal excretion. Approximately 85% of total body Pi is present in bone and only 1% is present as free Pi in extracellular fluids. In humans, extracellular concentrations of inorganic Pi vary between 0.8 and 1.2 mM, and in plasma or serum Pi exists in both its monovalent and divalent forms (HPO and HPO). In the intestine, approximately 30% of Pi absorption is vitamin D regulated and dependent. To help maintain Pi balance, reabsorption of filtered Pi along the renal proximal tubule (PT) is via the NaPi-IIa and NaPi-IIc Na-coupled Pi cotransporters, with a smaller contribution from the PiT-2 transporters. Endocrine factors, including, vitamin D and parathyroid hormone (PTH), as well as newer factors such as fibroblast growth factor (FGF)-23 and its coreceptor α-klotho, are intimately involved in the control of Pi homeostasis. A tight regulation of Pi is critical, since hyperphosphataemia is associated with increased cardiovascular morbidity in chronic kidney disease (CKD) and hypophosphataemia with rickets and growth retardation. This short review considers the control of Pi balance by vitamin D, PTH and Pi itself, with an emphasis on the insights gained from human genetic disorders and genetically modified mouse models.

摘要

无机磷酸盐(Pi)是体内含量丰富的元素,对于广泛的关键生物过程至关重要。它在细胞能量代谢和细胞信号传导中发挥重要作用,例如三磷酸腺苷(ATP)和三磷酸鸟苷(GTP),在磷脂膜和骨骼的组成中发挥重要作用,并且是 DNA 和 RNA 的组成部分。它是血液和尿液中的重要缓冲剂,有助于维持正常的酸碱平衡。鉴于其在几乎所有分子和细胞功能中的广泛作用,血清 Pi 水平和平衡的变化可能会产生重要的不利影响。通过肠道对 Pi 的饮食吸收、骨骼动员和肾脏排泄之间的平衡来维持 Pi 的体内平衡。大约 85%的总体内 Pi 存在于骨骼中,只有 1%以细胞外液中游离 Pi 的形式存在。在人类中,无机 Pi 的细胞外浓度在 0.8 和 1.2 mM 之间变化,并且在血浆或血清中,Pi 以单价和二价形式(HPO 和 HPO)存在。在肠道中,大约 30%的 Pi 吸收受维生素 D 调节和依赖。为了帮助维持 Pi 平衡,沿着肾近端小管(PT)对过滤的 Pi 进行重吸收是通过 NaPi-IIa 和 NaPi-IIc Na 偶联 Pi 共转运蛋白进行的,而 PiT-2 转运蛋白的贡献较小。内分泌因素,包括维生素 D 和甲状旁腺激素(PTH),以及新的因素,如成纤维细胞生长因子(FGF)-23 及其核心受体α-klotho,都密切参与 Pi 体内平衡的控制。对 Pi 的严格调节至关重要,因为高磷酸盐血症与慢性肾脏病(CKD)中的心血管发病率增加有关,而低磷酸盐血症与佝偻病和生长迟缓有关。这篇简短的综述考虑了维生素 D、PTH 和 Pi 本身对 Pi 平衡的控制,重点介绍了从人类遗传疾病和基因修饰小鼠模型中获得的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/914f/6326012/2fae47b11a7c/424_2018_2231_Fig1_HTML.jpg

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