Evidence map›Paper›PMID 19452240›Full record

ArticleClinical and experimental nephrology2009

Tolvaptan, a selective oral vasopressin V2 receptor antagonist, ameliorates podocyte injury in puromycin aminonucleoside nephrotic rats.

Tadashi Okada, Toshifumi Sakaguchi, Ikuji Hatamura, Fumie Saji, Shigeo Negi, Haruhisa Otani, Yasuteru Muragaki, Hiroshi Kawachi, Takashi Shigematsu

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In one paragraph

Article in Clinical and experimental nephrology, 2009. 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
0.9field-weighted citation impact, top 25% 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, 23 citations in OpenAlex.

  1. COVID-19 concomitant with infective endocarditis: A case report and review of management.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2020
    Review
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  6. Copeptin and Decline in Kidney Function.American journal of nephrology · 2016
    Article
  7. Article
  8. Vasopressin receptor antagonists.Current hypertension reports · 2015
    Review
  9. Article
  10. Observational
  11. Review
  12. Article
  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

9 authors at 2 institutions in 1 country.

Tadashi OkadaDivision of Nephrology and Blood Purification Medicine, Wakayama Medical University, 811-1, Kimiidera, Wakayama, 641-0012, Japan. tad-okada@umin.ac.jp.
Toshifumi SakaguchiDivision of Nephrology and Blood Purification Medicine, Wakayama Medical University, 811-1, Kimiidera, Wakayama, 641-0012, Japan.
Ikuji HatamuraFirst Department of Pathology, Wakayama Medical University, Wakayama, Japan.
Fumie SajiDivision of Nephrology and Blood Purification Medicine, Wakayama Medical University, 811-1, Kimiidera, Wakayama, 641-0012, Japan.
Shigeo NegiDivision of Nephrology and Blood Purification Medicine, Wakayama Medical University, 811-1, Kimiidera, Wakayama, 641-0012, Japan.
Haruhisa OtaniDivision of Nephrology and Blood Purification Medicine, Wakayama Medical University, 811-1, Kimiidera, Wakayama, 641-0012, Japan.
Yasuteru MuragakiFirst Department of Pathology, Wakayama Medical University, Wakayama, Japan.
Hiroshi KawachiDepartment of Cell Biology, Institute of Nephrology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Takashi ShigematsuDivision of Nephrology and Blood Purification Medicine, Wakayama Medical University, 811-1, Kimiidera, Wakayama, 641-0012, Japan.
Wakayama Medical University · JPNiigata University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProteinuria caused by glomerular disease is characterized by podocyte injury. Vasopressin V2 receptor antagonists are effective in reducing albuminuria, although their actions on glomerular podocytes have not been explored. The objective of this study was to evaluate the effects of tolvaptan, a selective oral V2 receptor antagonist, on podocytes in a puromycin aminonucleoside (PAN)-induced nephrosis rat model.

methodsRats were allocated to a control, PAN nephrosis, or tolvaptan-treated PAN nephrosis group (n = 9 per group). Urinary protein excretion and serum levels of total protein, albumin, creatinine, and total cholesterol were measured on day 10. The influence of tolvaptan on podocytes was examined in renal tissues by immunofluorescence and electron microscopy.

resultsPAN induced massive proteinuria and serum creatinine elevation on day 10, both of which were significantly ameliorated by tolvaptan. Immunofluorescence studies of the podocyte-associated proteins nephrin and podocin revealed granular staining patterns in PAN nephrosis rats. In tolvaptan-treated rats, nephrin and podocin expressions retained their normal linear pattern. Electron microscopy showed foot process effacement was ameliorated in tolvaptan-treated rats.

conclusionsTolvaptan is protective against podocyte damage and proteinuria in PAN nephrosis. This study indicates that tolvaptan exerts a renoprotective effect by affecting podocyte morphology and probably function in PAN nephrosis. Tolvaptan is a promising pharmacological tool in the treatment of renal edema.

Indexed as

Antidiuretic Hormone Receptor AntagonistsNephrosisAnimalsAntibiotics, AntineoplasticBenzazepinesDesminHumansIntracellular Signaling Peptides and ProteinsKidney GlomerulusMaleMembrane ProteinsOrgan SizePodocytesPuromycin AminonucleosideRatsRats, Sprague-DawleyAntibiotics, AntineoplasticAntidiuretic Hormone Receptor AntagonistsBenzazepinesDesminIntracellular Signaling Peptides and ProteinsMembrane ProteinsnephrinNPHS2 proteinPuromycin AminonucleosideTolvaptanWT1 Proteins

Identifiers

PMID19452240
OpenAlexW2054378298

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Registered trials

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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.