Evidence map›Paper›PMID 19675183›Full record

ArticleAmerican journal of physiology. Renal physiology2009

Regulation of rat intestinal Na-dependent phosphate transporters by dietary phosphate.

Hector Giral, Yupanqui Caldas, Eileen Sutherland, Paul Wilson, Sophia Breusegem, Nicholas Barry, Judith Blaine, Tao Jiang, Xiaoxin X Wang, Moshe Levi

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

65 citing papers in PubMed, 152 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Intestinal segment and vitamin DJournal of animal science and technology · 2023
    Article
  9. Article
  10. Article
  11. Phosphate intake, hyperphosphatemia, and kidney function.Pflugers Archiv : European journal of physiology · 2022
    Review
  12. Article
  13. Article
  14. Article
  15. Observational
  16. Article
  17. Article
  18. Phosphate Balance and CKD-Mineral Bone Disease.Kidney international reports · 2021
    Review
  19. Article
  20. Review

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

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

10 authors at 1 institution in 1 country.

Hector GiralDivision of Renal Diseases and Hypertension, Department of Medicine, University of Colorado Denver, and Veterans Affairs Medical Center, Aurora, CO 80045, USA. Hector.Giral-Arnal@ucdenver.edu
Yupanqui Caldas
Eileen Sutherland
Paul Wilson
Sophia Breusegem
Nicholas Barry
Judith Blaine
Tao Jiang
Xiaoxin X Wang
Moshe Levi
University of Colorado Denver · US

Funding

Regulation of Renal Phosphate Transport by LipidsR01DK066029 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI LEVI, MOSHE · 2005 to 2013
$3.2M
Role of FXR in Renal Disease of Metabolic Syndrome and AgingR01AG026529 · NIA · UNIVERSITY OF COLORADO DENVER · PI LEVI, MOSHE · 2007 to 2011
$1.8M
NIA NIH HHS 3R01 AG-026529NIDDK NIH HHS R01 DK-066029
6 · The paper itself

Abstract

Hyperphosphatemia associated with chronic kidney disease is one of the factors that can promote vascular calcification, and intestinal P(i) absorption is one of the pharmacological targets that prevents it. The type II Na-P(i) cotransporter NaPi-2b is the major transporter that mediates P(i) reabsorption in the intestine. The potential role and regulation of other Na-P(i) transporters remain unknown. We have identified expression of the type III Na-P(i) cotransporter PiT-1 in the apical membrane of enterocytes. Na-P(i) transport activity and NaPi-2b and PiT-1 proteins are mostly expressed in the duodenum and jejunum of rat small intestine; their expression is negligible in the ileum. In response to a chronic low-P(i) diet, there is an adaptive response restricted to the jejunum, with increased brush border membrane (BBM) Na-P(i) transport activity and NaPi-2b, but not PiT-1, protein and mRNA abundance. However, in rats acutely switched from a low- to a high-P(i) diet, there is an increase in BBM Na-P(i) transport activity in the duodenum that is associated with an increase in BBM NaPi-2b protein abundance. Acute adaptive upregulation is restricted to the duodenum and induces an increase in serum P(i) that produces a transient postprandial hyperphosphatemia. Our study, therefore, indicates that Na-P(i) transport activity and NaPi-2b protein expression are differentially regulated in the duodenum vs. the jejunum and that postprandial upregulation of NaPi-2b could be a potential target for treatment of hyperphosphatemia.

Indexed as

AnimalsBlotting, WesternCell MembraneDuodenumEnterocytesIntestine, SmallJejunumMaleMicroscopy, FluorescenceMicrovilliPhosphatesPhosphorus, DietaryRatsRats, Sprague-DawleyRNA, MessengerSodium-Phosphate Cotransporter ProteinsPhosphatesPhosphorus, DietaryRNA, MessengerSlc20a1 protein, ratSlc34a2 protein, ratSodium-Phosphate Cotransporter ProteinsSodium-Phosphate Cotransporter Proteins, Type IIbSodium-Phosphate Cotransporter Proteins, Type III

Identifiers

PMID19675183
PMCPMC2781338
OpenAlexW1963541108

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.