Evidence map›Paper›PMID 23863468›Full record

ArticleAmerican journal of physiology. Renal physiology2013

Renalase regulates renal dopamine and phosphate metabolism.

Daria Sizova, Heino Velazquez, Benedita Sampaio-Maia, Janete Quelhas-Santos, Manuel Pestana, Gary V Desir

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

13 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Renalase alleviates salt-induced kidney necroptosis and inflammation.Hypertension research : official journal of the Japanese Society of Hypertension · 2024
    Article
  3. The Intricacies of Renal Phosphate Reabsorption-An Overview.International journal of molecular sciences · 2024
    Review
  4. Article
  5. Article
  6. Where Is Dopamine and how do Immune Cells See it?: Dopamine-Mediated Immune Cell Function in Health and Disease.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2020
    Review
  7. Extracellular renalase protects cells and organs by outside-in signalling.Journal of cellular and molecular medicine · 2017
    Review
  8. Review
  9. Article
  10. Antihypertensive mechanisms of intra-renal dopamine.Current opinion in nephrology and hypertension · 2015
    Review
  11. Renalase regulates peripheral and central dopaminergic activities.American journal of physiology. Renal physiology · 2015
    Article
  12. Regulation of serum phosphate.The Journal of physiology · 2014
    Review
  13. 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

6 authors at 3 institutions in 2 countries.

Daria SizovaSection of Nephrology, Dept. of Medicine, Yale School of Medicine, P.O. Box 208029, New Haven, CT 06520-8029. gary.desir@yale.edu.
Heino Velazquez
Benedita Sampaio-Maia
Janete Quelhas-Santos
Manuel Pestana
Gary V Desir
VA Connecticut Research and Education Foundation · USUniversidade do Porto · PTHospital de São João · PT

Funding

Renal Physiology and Phenotyping CoreP30DK079310 · NIDDK · YALE UNIVERSITY · PI SOMLO, STEFAN · 2008 to 2022
$16.8M
The Molecular Physiology of RenalaseR01DK081037 · NIDDK · YALE UNIVERSITY · PI DESIR, GARY V. · 2009 to 2010
$646k
RENALASE DEFICIENCY AND CARDIOVASCULAR COMPLICATIONS OF CHRONIC KIDNEY DISEASERC1DK086402 · NIDDK · YALE UNIVERSITY · PI DESIR, GARY V. · 2010 to 2010
$500k
RENALASE IN ACUTE KIDNEY INJURY: UTILITY AS A BIOMARKER, AND THERAPEUTIC AGENTRC1DK086465 · NIDDK · YALE UNIVERSITY · PI DESIR, GARY V. · 2010 to 2010
$500k
NIDDK NIH HHS P30 DK079310NIDDK NIH HHS R01 DK-081037NIDDK NIH HHS RC1 DK-086402NIDDK NIH HHS RC1 DK-086465
6 · The paper itself

Abstract

Renalase is a kidney-secreted catecholamines-degrading enzyme whose expression and activity are downregulated by increased dietary phosphate. A renalase knockout (KO) mouse model was used to explore the mechanisms mediating renalase's effect on phosphate excretion. Compared with wild-type (WT) mice maintained on a regular diet, KO mice show decreased serum PO4(-) (KO = 5.3 ± 0.2 vs. WT = 6.0 ± 0.1, n = 6; P < 0.04) and increased urinary PO4(-) excretion (urine PO4(-)/creatinine: KO = 7.7 ± 0.3 vs. WT = 6.1 ± 0.3, n = 6; P < 0.02). However, both WT and KO mice respond similarly to PO4(-) restriction by increasing renal COMT-1 activity and markedly decreasing PO4(-) excretion, which excludes an intrinsic renal defect in the KO. Renal sodium-phosphate cotransporter Npt2a, sodium proton exchanger NHE3 expression, and MAO-A and B activity did not differ between WT and KO. Only catechol-O-methyl transferase (COMT) expression and activity were significantly increased in KO mice. Despite that, urinary dopamine increased by twofold, whereas urinary l-DOPA excretion decreased by twofold in the KO mouse, indicating an upregulation of renal dopamine (DA) synthesis. These data indicate that renalase deficiency is associated with increased renal DA synthesis, stimulated PO4(-) excretion, and moderately severe hypophosphatemia. The signal to increase renal DA synthesis is strong since it overcomes a compensatory increase in COMT activity.

Indexed as

AnimalsCatechol O-MethyltransferaseCreatinineDopamineHypophosphatemiaKidneyLevodopaMiceMice, KnockoutMonoamine OxidasePhosphatesCatechol O-MethyltransferaseCreatinineDopamineLevodopaMonoamine OxidasePhosphatesrenalasedopaminephosphate regulationrenalase

Identifiers

PMID23863468
PMCPMC3761288
OpenAlexW2034116459

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.