Evidence map›Paper›PMID 21451460›Full record

ArticleKidney international2011

Decreased bone density and increased phosphaturia in gene-targeted mice lacking functional serum- and glucocorticoid-inducible kinase 3.

Madhuri Bhandaru, Daniela S Kempe, Anand Rotte, Paola Capuano, Ganesh Pathare, Mentor Sopjani, Ioana Alesutan, Leonid Tyan, Dan Yang Huang, Balasaheb Siraskar and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in Kidney international, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

17 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Contributions of SGK3 to transporter-related diseases.Frontiers in cell and developmental biology · 2022
    Review
  7. Article
  8. Congenital Conditions of Hypophosphatemia in Children.Calcified tissue international · 2021
    Review
  9. Article
  10. Insulin suppresses the production of fibroblast growth factor 23 (FGF23).Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  11. Lack of serum- and glucocorticoid-inducible kinase 3 leads to podocyte dysfunction.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2018
    Article
  12. Enhanced FGF23 production in mice expressing PI3K-insensitive GSK3 is normalized by β-blocker treatment.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2016
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 2 institutions in 2 countries.

Madhuri BhandaruDepartment of Physiology, University of Tübingen, Tübingen, Germany.
Daniela S Kempe
Anand Rotte
Paola Capuano
Ganesh Pathare
Mentor Sopjani
Ioana Alesutan
Leonid Tyan
Dan Yang Huang
Balasaheb Siraskar
Martin S Judenhofer
Gerti Stange
Bernd J Pichler
Jürg Biber
Leticia Quintanilla-Martinez
Carsten A Wagner
David Pearce
Michael Föller
Florian Lang
University of Tübingen · DEUniversity of California, San Francisco · US

Funding

SGK Regulation of Epithelial Sodium TransportR01DK056695 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI DAVID PEARCE · 2000 to 2026
$8.1M
NIDDK NIH HHS R01 DK056695
6 · The paper itself

Abstract

Insulin and growth factors activate the phosphatidylinositide-3-kinase pathway, leading to stimulation of several kinases including serum- and glucocorticoid-inducible kinase isoform SGK3, a transport regulating kinase. Here, we explored the contribution of SGK3 to the regulation of renal tubular phosphate transport. Coexpression of SGK3 and sodium-phosphate cotransporter IIa significantly enhanced the phosphate-induced current in Xenopus oocytes. In sgk3 knockout and wild-type mice on a standard diet, fluid intake, glomerular filtration and urine flow rates, and urinary calcium ion excretion were similar. However, fractional urinary phosphate excretion was slightly but significantly larger in the knockout than in wild-type mice. Plasma calcium ion, phosphate concentration, and plasma parathyroid hormone levels were not significantly different between the two genotypes, but plasma calcitriol and fibroblast growth factor 23 concentrations were significantly lower in the knockout than in wild-type mice. Moreover, bone density was significantly lower in the knockouts than in wild-type mice. Histological analysis of the femur did not show any differences in cortical bone but there was slightly less prominent trabecular bone in sgk3 knockout mice. Thus, SGK3 has a subtle but significant role in the regulation of renal tubular phosphate transport and bone density.

Indexed as

AnimalsBiological Transport, ActiveBone DensityCalciumFemaleHumansHypophosphatemia, FamilialIn Vitro TechniquesKidney TubulesMiceMice, KnockoutOocytesPhosphatesProtein Serine-Threonine KinasesRecombinant ProteinsSerum-Glucocorticoid Regulated KinasesCalciumPhosphatesProtein Serine-Threonine KinasesRecombinant ProteinsSerum-Glucocorticoid Regulated KinasesSGK3 protein, humanSgk3 protein, mouseSLC34A1 protein, humanSodium-Phosphate Cotransporter Proteins, Type IIa

Identifiers

PMID21451460
PMCPMC6049080
OpenAlexW2071841729

What OpenQuestion holds

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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.