Evidence map›Paper›PMID 27327879›Full record

ArticlePloS one2016

Protection of the Transplant Kidney from Preservation Injury by Inhibition of Matrix Metalloproteinases.

Michael A J Moser, Steve Arcand, Han-Bin Lin, Chris Wojnarowicz, Jolanta Sawicka, Tamalina Banerjee, Yigang Luo, Gavin R Beck, Patrick P Luke, Grzegorz Sawicki

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

26 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Delivery of a Muscle-Targeted Adeno-Associated Vector ViaTransplant international : official journal of the European Society for Organ Transplantation · 2025
    Article
  5. Review
  6. Human gene therapy · 2024
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Sense and Sensibilities of Organ Perfusion as a Kidney and Liver Viability Assessment Platform.Transplant international : official journal of the European Society for Organ Transplantation · 2022
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Frontiers in medicine · 2021
    Review
  17. Article
  18. Review
  19. Article
  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

10 authors at 5 institutions in 2 countries.

Michael A J MoserDepartment of Surgery and Saskatchewan Renal Transplant Program, Saskatoon, Saskatchewan.ORCID http://orcid.org/0000-0003-0735-199X
Steve ArcandDepartment of Pharmacology, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Han-Bin LinDepartment of Pharmacology, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Chris WojnarowiczPrairie Diagnostic Services, Department of Veterinary Pathology, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Jolanta SawickaDepartment of Pharmacology, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Tamalina BanerjeeDepartment of Laboratory Medicine and Pathology, Saskatoon Health Region, Saskatoon, Saskatchewan, Canada.
Yigang LuoDepartment of Surgery and Saskatchewan Renal Transplant Program, Saskatoon, Saskatchewan.
Gavin R BeckDepartment of Surgery and Saskatchewan Renal Transplant Program, Saskatoon, Saskatchewan.
Patrick P LukeMulti Organ Transplant Program, London Health Sciences Centre, London, Ontario, Canada.
Grzegorz SawickiDepartment of Pharmacology, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
University of Saskatchewan · CALondon Health Sciences Centre · CASaskatchewan Health Authority · CAUniversity of Ottawa · CAUniversity of Wrocław · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMatrix metalloproteinases (MMPs), particularly MMP-2 and MMP-9, play an important role in ischemic injury to the heart, yet it is not known if these MMPs are involved in the injury that occurs to the transplant kidney. We therefore studied the pharmacologic protection of transplant kidneys during machine cold perfusion.

methodsHuman kidney perfusates were analyzed for the presence of injury markers such as cytochrome c oxidase, lactate dehydrogenase, and neutrophil-gelatinase associated lipocalin (NGAL), and MMP-2 and MMP-9 were measured. The effects of MMP inhibitors MMP-2 siRNA and doxycycline were studied in an animal model of donation after circulatory determination of death (DCDD).

resultsMarkers of injury were present in all analyzed perfusates, with higher levels seen in perfusates from human kidneys donated after controlled DCDD compared to brain death and in perfusate from kidneys with delayed graft function. When rat kidneys were perfused at 4°C for 22 hours with the addition of MMP inhibitors, this resulted in markedly reduced levels of MMP-2, MMP-9 and analyzed injury markers.

conclusionsBased on our study, MMPs are involved in preservation injury and the supplementation of preservation solution with MMP inhibitors is a potential novel strategy in protecting the transplant kidney from preservation injury.

Indexed as

Kidney TransplantationOrgan PreservationAdultAnimalsBiomarkersDelayed Graft FunctionDoxycyclineElectron Transport Complex IVFemaleHumansKidneyLipocalin-2L-Lactate DehydrogenaseMaleMatrix Metalloproteinase 2Matrix Metalloproteinase 9BiomarkersDoxycyclineElectron Transport Complex IVLipocalin-2L-Lactate DehydrogenaseMatrix Metalloproteinase 2Matrix Metalloproteinase 9Matrix Metalloproteinase InhibitorsMatrix Metalloproteinases

Identifiers

PMID27327879
PMCPMC4915675
OpenAlexW2474272310

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.