Evidence map›Paper›PMID 27056295›Full record

ArticleJournal of the American Society of Nephrology : JASN2017

σ1-Receptor Agonism Protects against Renal Ischemia-Reperfusion Injury.

Adam Hosszu, Zsuzsanna Antal, Lilla Lenart, Judit Hodrea, Sandor Koszegi, Dora B Balogh, Nora F Banki, Laszlo Wagner, Adam Denes, Peter Hamar and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

33 citing papers in PubMed, 59 citations in OpenAlex.

  1. Trial
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  5. Review
  6. Article
  7. The Potential Renoprotective Effect of Sugammadex in Renal Ischemia-reperfusion Injury.Turkish journal of anaesthesiology and reanimation · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Sigma-1 Receptor as a Novel Therapeutic Target in Diabetic Kidney Disease.International journal of molecular sciences · 2024
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
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  20. 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

14 authors at 2 institutions in 1 country.

Adam HosszuMTA-SE Lendulet Diabetes Research Group and.
Zsuzsanna AntalFirst Department of Pediatrics.
Lilla LenartMTA-SE Lendulet Diabetes Research Group and.
Judit HodreaMTA-SE Lendulet Diabetes Research Group and.
Sandor KoszegiMTA-SE Lendulet Diabetes Research Group and.
Dora B BaloghMTA-SE Lendulet Diabetes Research Group and.
Nora F BankiFirst Department of Pediatrics.
Laszlo WagnerDepartment of Transplantation and Surgery, and.
Adam DenesLaboratory of Neuroimmunology, Institute of Experimental Medicine, Budapest, Hungary; and.
Peter HamarInstitute of Pathophysiology, Semmelweis University, Budapest, Hungary.
Peter DegrellDepartment of Pathology, Moritz Kaposi General Hospital, Kaposvar, Hungary.
Adam VannayMTA-SE Pediatrics and Nephrology Research Group, Hungarian Academy of Sciences and Semmelweis University, Budapest, Hungary.
Attila J SzaboFirst Department of Pediatrics.
Andrea FeketeMTA-SE Lendulet Diabetes Research Group and fekete.andrea@med.semmelweis-univ.hu.
Semmelweis University · HUHUN-REN Institute of Experimental Medicine · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mechanisms of renal ischemia-reperfusion injury remain unresolved, and effective therapies are lacking. We previously showed that dehydroepiandrosterone protects against renal ischemia-reperfusion injury in male rats. Here, we investigated the potential role of σ1-receptor activation in mediating this protection. In rats, pretreatment with either dehydroepiandrosterone or fluvoxamine, a high-affinity σ1-receptor agonist, improved survival, renal function and structure, and the inflammatory response after sublethal renal ischemia-reperfusion injury. In human proximal tubular epithelial cells, stimulation by fluvoxamine or oxidative stress caused the σ1-receptor to translocate from the endoplasmic reticulum to the cytosol and nucleus. Fluvoxamine stimulation in these cells also activated nitric oxide production that was blocked by σ1-receptor knockdown or Akt inhibition. Similarly, in the postischemic rat kidney, σ1-receptor activation by fluvoxamine triggered the Akt-nitric oxide synthase signaling pathway, resulting in time- and isoform-specific endothelial and neuronal nitric oxide synthase activation and nitric oxide production. Concurrently, intravital two-photon imaging revealed prompt peritubular vasodilation after fluvoxamine treatment, which was blocked by the σ1-receptor antagonist or various nitric oxide synthase blockers. In conclusion, in this rat model of ischemia-reperfusion injury, σ1-receptor agonists improved postischemic survival and renal function via activation of Akt-mediated nitric oxide signaling in the kidney. Thus, σ1-receptor activation might provide a therapeutic option for renoprotective therapy.

Indexed as

Acute Kidney InjuryAnimalsDehydroepiandrosteroneFluvoxamineKidneyMaleRatsRats, WistarReceptors, sigmaReperfusion InjurySelective Serotonin Reuptake InhibitorsSigma-1 ReceptorDehydroepiandrosteroneFluvoxamineReceptors, sigmaSelective Serotonin Reuptake InhibitorsSigma-1 Receptorischemia-reperfusionkidneynitric oxideSigma-1 receptor

Identifiers

PMID27056295
PMCPMC5198266
OpenAlexW2325525149

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.