Evidence map›Paper›PMID 26847569›Full record

ArticleJournal of translational medicine2016

Effectiveness of pure argon for renal transplant preservation in a preclinical pig model of heterotopic autotransplantation.

Alice Faure, Laurie Bruzzese, Jean-Guillaume Steinberg, Yves Jammes, Julia Torrents, Stephane V Berdah, Emmanuelle Garnier, Tristan Legris, Anderson Loundou, Matthieu Chalopin and 4 more

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.5field-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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. [Research progress on preventions of ischemia-reperfusion injury during kidney transplant].Sheng wu yi xue gong cheng xue za zhi = Journal of biomedical engineering = Shengwu yixue gongchengxue zazhi · 2018
    Review
  13. Review
  14. A porcineMedical gas research
    Article
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 6 institutions in 2 countries.

Alice FaureDepartment of Urology and Kidney Transplantation, Aix-Marseille University, APHM, Marseille, France. alice.faure@ap-hm.fr.
Laurie BruzzeseUMR MD2 & IRBA, Aix-Marseille University, Marseille, France. laurie.bruzzese@gmail.com.
Jean-Guillaume SteinbergUMR MD2 & IRBA, Aix-Marseille University, Marseille, France. jean.steinberg@univ-amu.fr.
Yves JammesUMR MD2 & IRBA, Aix-Marseille University, Marseille, France. yves.jammes@unvi-amu.fr.
Julia TorrentsDepartment of Pathology, Aix-Marseille University, APHM, Marseille, France. julia.torrents@ap-hm.fr.
Stephane V BerdahC.E.R.C, Aix-Marseille University, Faculty of Medicine, Marseille, France. stephane.berdah@ap-hm.fr.
Emmanuelle GarnierC.E.R.C, Aix-Marseille University, Faculty of Medicine, Marseille, France. emmanuelle.garnier2@wanadoo.fr.
Tristan LegrisDepartment of Nephrology and Kidney Transplantation, Aix-Marseille University, APHM, Marseille, France. tristan.legris@ap-hm.fr.
Anderson LoundouPublic Health Laboratory, Aix-Marseille University, Marseille, France. anderson.loundou@univ-amu.fr.
Matthieu ChalopinAir Liquide Medical Gases Group, Air Liquide sante International-Claude Delorme Research Center, Jouy-en-Josas, France. matthieu.chalopin@airliquide.com.
Guy MagalonDepartment of Plastic Surgery, Aix-Marseille University, APHM, Marseille, France. guy.magalon@gmail.com.
Regis GuieuUMR MD2 & IRBA, Aix-Marseille University, Marseille, France. guieu.regis@orange.fr.
Emmanuel FenouilletUMR MD2 & IRBA, Aix-Marseille University, Marseille, France. emmanuel.fenouillet@univ-amu.fr.
Eric LechevallierDepartment of Urology and Kidney Transplantation, Aix-Marseille University, APHM, Marseille, France. eric.lechevallier@ap-hm.fr.
Aix-Marseille Université · FRAssistance Publique Hôpitaux de Marseille · FRHôpital de la Conception · FRHôpital Nord · FRIfremer · FRInstitut de Neurophysiopathologie · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn kidney transplantation, the conditions of organ preservation following removal influence function recovery. Current static preservation procedures are generally based on immersion in a cold-storage solution used under atmospheric air (approximately 78 kPa N2, 21 kPa O2, 1 kPa Ar). Research on static cold-preservation solutions has stalled, and modifying the gas composition of the storage medium for improving preservation was considered. Organoprotective strategies successfully used noble gases and we addressed here the effects of argon and xenon on graft preservation in an established preclinical pig model of autotransplantation.

methodsThe preservation solution Celsior saturated with pure argon (Argon-Celsior) or xenon (Xenon-Celsior) at atmospheric pressure was tested versus Celsior saturated with atmospheric air (Air-Celsior). The left kidney was removed, and Air-Celsior (n = 8 pigs), Argon-Celsior (n = 8) or Xenon-Celsior (n = 6) was used at 4 °C to flush and store the transplant for 30 h, a duration that induced ischemic injury in our model when Air-Celsior was used. Heterotopic autotransplantation and contralateral nephrectomy were performed. Animals were followed for 21 days.

resultsThe use of Argon-Celsior vs. Air-Celsior: (1) improved function recovery as monitored via creatinine clearance, the fraction of excreted sodium and tubulopathy duration; (2) enabled diuresis recovery 2-3 days earlier; (3) improved survival (7/8 vs. 3/8 pigs survived at postoperative day-21); (4) decreased tubular necrosis, interstitial fibrosis, apoptosis and inflammation, and preserved tissue structures as observed after the natural death/euthanasia; (5) stimulated plasma antioxidant defences during the days following transplantation as shown by monitoring the "reduced ascorbic acid/thiobarbituric acid reactive substances" ratio and Hsp27 expression; (6) limited the inflammatory response as shown by expression of TNF-alpha, IL1-beta and IL6 as observed after the natural death/euthanasia. Conversely, Xenon-Celsior was detrimental, no animal surviving by day-8 in a context where functional recovery, renal tissue properties and the antioxidant and inflammation responses were significantly altered. Thus, the positive effects of argon were not attributable to the noble gases as a group.

conclusionsThe saturation of Celsior with argon improved early functional recovery, graft quality and survival. Manipulating the gas composition of a preservation medium constitutes therefore a promising approach to improve preservation.

Indexed as

Kidney TransplantationOrgan PreservationAirAnimalsAntioxidantsArgonDisaccharidesElectrolytesEpithelial CellsFemaleGlutamatesGlutathioneGraft SurvivalHistidineInflammationMannitolAntioxidantsArgonCelsiorDisaccharidesElectrolytesGlutamatesGlutathioneHistidineMannitolXenon

Identifiers

PMID26847569
PMCPMC4743167
OpenAlexW2271037647

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.