Evidence map›Paper›PMID 18645497›Full record

ArticleTransplantation2008

Improvement of canine islet yield by donor pancreas infusion with a p38MAPK inhibitor.

Taihei Ito, Keiko Omori, Jeffrey Rawson, Ivan Todorov, Sadaki Asari, Akio Kuroda, Jonathan Shintaku, Shin Itakura, Kevin Ferreri, Fouad Kandeel and 1 more

Abstract read
In one paragraph

Article in Transplantation, 2008. 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
2.1field-weighted citation impact, top 13% 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, 29 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Regulation of c-Jun NHJournal of clinical medicine · 2019
    Review
  7. Involvement of a proapoptotic gene (BBC3) in islet injury mediated by cold preservation and rewarming.American journal of physiology. Endocrinology and metabolism · 2016
    Article
  8. Article
  9. Article
  10. Laser scanning cytometry: principles and applications-an update.Methods in molecular biology (Clifton, N.J.) · 2013
    Review
  11. Article
  12. Article
  13. 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

11 authors at 1 institution in 1 country.

Taihei ItoSouthern California Islet Cell Resources Center, Department of Diabetes, Endocrinology and Metabolism, Beckman Research Institute of the City of Hope, Duarte, CA 91010, USA.
Keiko Omori
Jeffrey Rawson
Ivan Todorov
Sadaki Asari
Akio Kuroda
Jonathan Shintaku
Shin Itakura
Kevin Ferreri
Fouad Kandeel
Yoko Mullen
City Of Hope National Medical Center · US

Funding

SOUTHERN CALIFORNIA ISLET CELL RESOURCES (SCI-ICR) CENTERU42RR016607 · NCRR · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI RIGGS, ARTHUR D · 2001 to 2009
$6.6M
NCRR NIH HHS U42 RR016607NCRR NIH HHS U42 RR 16607
6 · The paper itself

Abstract

backgroundThe activation of p38 mitogen-activated protein kinases (MAPK) is implicated in cold ischemia-reperfusion injury of donor organs. The islet isolation process, from pancreas procurement through islet collection, may activate p38MAPK leading to cytokine release and islet damage. This damage may be prevented by treating pancreata with a p38MAPK inhibitor (p38IH) before cold preservation.

methodsPancreata removed from Beagle dogs were infused with University of Wisconsin solution containing the p38IH, SB203580, and Pefabloc (n=6) or vehicle (dimethyl sulfoxide and Pefabloc) alone (n=7), through the pancreatic duct and preserved using the two-layer method. After 20 to 22 hr, islets were isolated and 3000 IEQ/kg were autotransplanted into the corresponding dog to monitor glucose metabolism.

resultsp38IH-treated pancreata yielded significantly more islets than control pancreata (IEQ/g: 2134+/-297 vs. 1477+/-145 IEQ/g or 65,012+/-9385 vs. 45,700+/-5103 IEQ/pancreas; P<0.05). Apoptotic beta-cell percentages assessed by laser scanning cytometry were lower in p38IH-treated than the controls (44%+/-9.4% vs. 61.6%+/-4.8%, P<0.05). Tumor necrosis factor-alpha expression assessed by real-time reverse transcription polymerase chain reaction was significantly lower in the p38IH-treated group than controls. All dogs (3000 IEQ/kg) transplanted with p38IH-treated islets (n=5) became euglycemic versus four of five dogs that received untreated islets. Plasma C-peptide levels after glucagon challenge were higher in animals receiving p38IH-treated islets (n=5) versus untreated islets (n=4) (0.40+/-0.78 vs. 0.21+/-0.05 ng/mL, P<0.05).

conclusionsInfusion of pancreata with University of Wisconsin solution containing p38IH through the duct before preservation suppresses cytokine release, prevents beta-cell apoptosis, and improves islet yield significantly with no adverse effect on islet function after transplantation. p38IH treatment of human pancreata may improve islet yield for use in clinical transplantation.

Indexed as

ApoptosisAdenosineAllopurinolAnimalsCytokinesDogsEnzyme ActivationEnzyme InhibitorsGlutathioneInsulinInsulin-Secreting CellsIslets of LangerhansIslets of Langerhans TransplantationMaleOrgan PreservationOrgan Preservation SolutionsAdenosineAllopurinolCytokinesEnzyme InhibitorsGlutathioneInsulinOrgan Preservation Solutionsp38 Mitogen-Activated Protein KinasesRaffinoseUniversity of Wisconsin-lactobionate solution

Identifiers

PMID18645497
PMCPMC3791927
OpenAlexW2021230180

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.