Evidence map›Paper›PMID 17566100›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2007

Evidence for a signaling axis by which intestinal phosphate rapidly modulates renal phosphate reabsorption.

Theresa Berndt, Leslie F Thomas, Theodore A Craig, Stacy Sommer, Xujian Li, Eric J Bergstralh, Rajiv Kumar

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
6.0field-weighted citation impact, top 4% of its field
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

68 citing papers in PubMed, 175 citations in OpenAlex.

  1. Trial
  2. Cardiovascular effects of sevelamer in stage 3 CKD.Journal of the American Society of Nephrology : JASN · 2013
    Trial
  3. Trial
  4. Structures of the sodium-coupled phosphate importer SLC34A2 reveal a distinct architecture and gating mechanism.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Observational
  14. Article
  15. Review
  16. Phosphate as a Signaling Molecule.Calcified tissue international · 2021
    Review
  17. Article
  18. Article
  19. The role of SLC34A2 in intestinal phosphate absorption and phosphate homeostasis.Pflugers Archiv : European journal of physiology · 2019
    Review
  20. Article

8 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

Theresa BerndtDivision of Nephrology and Hypertension, Department of Internal Medicine, Mayo Clinic, 200 First Street Southwest, Rochester, MN 55905, USA.
Leslie F Thomas
Theodore A Craig
Stacy Sommer
Xujian Li
Eric J Bergstralh
Rajiv Kumar
Hypertension Institute · USDepartment of Medical Sciences · BYMayo Clinic · US

Funding

REGULATIOIN OF RENAL PHOSPHATE EXCRETION AND VITAMIN D METABOLISM BY FGF 7R01DK076829 · NIDDK · MAYO CLINIC ROCHESTER · PI KUMAR, RAJIV · 2007 to 2010
$1.2M
Biology of a Novel Phosphaturic Protein - sFRP-4R01DK065830 · NIDDK · MAYO CLINIC ROCHESTER · PI KUMAR, RAJIV · 2004 to 2007
$1.2M
Hyperoxaluria and Nephrolithiasis After Gastric Bypass Surgery for ObesityR21DK077669 · NIDDK · MAYO CLINIC ROCHESTER · PI KUMAR, RAJIV · 2007 to 2008
$412k
EXPRESSION AND STRUCTURE OF THE CALCIUM SENSING RECEPTORR21DK073369 · NIDDK · MAYO CLINIC ROCHESTER · PI KUMAR, RAJIV · 2006 to 2007
$292k
NIDDK NIH HHS DK65830NIDDK NIH HHS DK73369NIDDK NIH HHS R01 DK065830NIDDK NIH HHS R01 DK076829NIDDK NIH HHS R21 DK073369NIDDK NIH HHS R21 DK077669
6 · The paper itself

Abstract

The mechanisms by which phosphorus homeostasis is preserved in mammals are not completely understood. We demonstrate the presence of a mechanism by which the intestine detects the presence of increased dietary phosphate and rapidly increases renal phosphate excretion. The mechanism is of physiological relevance because it maintains plasma phosphate concentrations in the normal range after ingestion of a phosphate-containing meal. When inorganic phosphate is infused into the duodenum, there is a rapid increase in the renal fractional excretion of phosphate (FE Pi). The phosphaturic effect of intestinal phosphate is specific for phosphate because administration of sodium chloride does not elicit a similar response. Phosphaturia after intestinal phosphate administration occurs in thyro-parathyroidectomized rats, demonstrating that parathyroid hormone is not essential for this effect. The increase in renal FE Pi in response to the intestinal administration of phosphate occurs without changes in plasma concentrations of phosphate (filtered load), parathyroid hormone, FGF-23, or secreted frizzled related protein-4. Denervation of the kidney does not attenuate phosphaturia elicited after intestinal phosphate administration. Phosphaturia is not elicited when phosphate is instilled in other parts of the gastrointestinal tract such as the stomach. Infusion of homogenates of the duodenal mucosa increases FE Pi, which demonstrates the presence of one or more substances within the intestinal mucosa that directly modulate renal phosphate reabsorption. Our experiments demonstrate the presence of a previously unrecognized phosphate gut-renal axis that rapidly modulates renal phosphate excretion after the intestinal administration of phosphate.

Indexed as

AbsorptionAnimalsDuodenumIntestinal AbsorptionIntestinal MucosaKidneyParathyroidectomyPhosphatesRatsPhosphates

Identifiers

PMID17566100
PMCPMC1891094
OpenAlexW2020162188

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.