Evidence map›Paper›PMID 23708836›Full record

ArticlePflugers Archiv : European journal of physiology2013

The phosphate transporter NaPi-IIa determines the rapid renal adaptation to dietary phosphate intake in mouse irrespective of persistently high FGF23 levels.

Soline Bourgeois, Paola Capuano, Gerti Stange, Reto Mühlemann, Heini Murer, Jürg Biber, Carsten A Wagner

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Article in Pflugers Archiv : European journal of physiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Acute Adaption to Oral or Intravenous Phosphate Requires Parathyroid Hormone.Journal of the American Society of Nephrology : JASN · 2017
    Article
  12. Article
  13. Systemic Control of Bone Homeostasis by FGF23 Signaling.Current molecular biology reports · 2016
    Article
  14. Article
  15. Proteinuria Increases Plasma Phosphate by Altering Its Tubular Handling.Journal of the American Society of Nephrology : JASN · 2015
    Article
  16. Article
  17. Regulation of renal phosphate transport by FGF23 is mediated by FGFR1 and FGFR4.American journal of physiology. Renal physiology · 2014
    Article
  18. The SLC34 family of sodium-dependent phosphate transporters.Pflugers Archiv : European journal of physiology · 2014
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Soline BourgeoisInstitute of Physiology and Zurich Center for Integrative Human Physiology (ZIHP), University of Zürich, Winterthurerstrasse 190, CH-8057, Zurich, Switzerland.
Paola Capuano
Gerti Stange
Reto Mühlemann
Heini Murer
Jürg Biber
Carsten A Wagner

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Renal reabsorption of inorganic phosphate (Pi) is mediated by the phosphate transporters NaPi-IIa, NaPi-IIc, and Pit-2 in the proximal tubule brush border membrane (BBM). Dietary Pi intake regulates these transporters; however, the contribution of the specific isoforms to the rapid and slow phase is not fully clarified. Moreover, the regulation of PTH and FGF23, two major phosphaturic hormones, during the adaptive phase has not been correlated. C57/BL6 and NaPi-IIa(-/-) mice received 5 days either 1.2 % (HPD) or 0.1 % (LPD) Pi-containing diets. Thereafter, some mice were acutely switched to LPD or HPD. Plasma Pi concentrations were similar under chronic diets, but lower when mice were acutely switched to LPD. Urinary Pi excretion was similar in C57/BL6 and NaPi-IIa(-/-) mice under HPD. During chronic LPD, NaPi-IIa(-/-) mice lost phosphate in urine compensated by higher intestinal Pi absorption. During the acute HPD-to-LPD switch, NaPi-IIa(-/-) mice exhibited a delayed decrease in urinary Pi excretion. PTH was acutely regulated by low dietary Pi intake. FGF23 did not respond to low Pi intake within 8 h whereas the phospho-adaptator protein FRS2α necessary for FGF-receptor cell signaling was downregulated. BBM Pi transport activity and NaPi-IIa but not NaPi-IIc and Pit-2 abundance acutely adapted to diets in C57/BL6 mice. In NaPi-IIa(-/-), Pi transport activity was low and did not adapt. Thus, NaPi-IIa mediates the fast adaptation to Pi intake and is upregulated during the adaptation to low Pi despite persistently high FGF23 levels. The sensitivity to FGF23 may be regulated by adapting FRS2α abundance and phosphorylation.

Indexed as

Adaptation, PhysiologicalAdaptor Proteins, Signal TransducingAnimalsFibroblast Growth Factor-23Fibroblast Growth FactorsIntestinal AbsorptionKidney Tubules, ProximalMembrane ProteinsMiceMice, Inbred C57BLMice, KnockoutPhosphorus, DietarySodium-Phosphate Cotransporter Proteins, Type IIaAdaptor Proteins, Signal TransducingFGF23 protein, humanFgf23 protein, mouseFibroblast Growth Factor-23Fibroblast Growth FactorsFRS2alpha protein, mouseMembrane ProteinsPhosphorus, DietarySlc34a1 protein, mouseSodium-Phosphate Cotransporter Proteins, Type IIa

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.