Evidence map›Paper›PMID 31291121›Full record

ArticleAmerican journal of physiology. Renal physiology2019

A mouse model of renal ischemia-reperfusion injury solely induced by cold ischemia.

Jin Wei, Yingliang Wang, Jie Zhang, Lei Wang, Liying Fu, Byeong J Cha, Jacentha Buggs, Ruisheng Liu

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2019. 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
2.9field-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

14 citing papers in PubMed, 27 citations in OpenAlex.

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  13. Protein Kinase C-Journal of the American Society of Nephrology : JASN · 2020
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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

8 authors at 3 institutions in 1 country.

Jin WeiDepartment of Molecular Pharmacology and Physiology, University of South Florida College of Medicine, Tampa, Florida.
Yingliang WangDepartment of Molecular Pharmacology and Physiology, University of South Florida College of Medicine, Tampa, Florida.
Jie ZhangDepartment of Molecular Pharmacology and Physiology, University of South Florida College of Medicine, Tampa, Florida.
Lei WangDepartment of Molecular Pharmacology and Physiology, University of South Florida College of Medicine, Tampa, Florida.
Liying FuTampa General Hospital, Tampa, Florida.
Byeong J ChaDepartment of Molecular Pharmacology and Physiology, University of South Florida College of Medicine, Tampa, Florida.
Jacentha BuggsTampa General Hospital, Tampa, Florida.
Ruisheng LiuDepartment of Molecular Pharmacology and Physiology, University of South Florida College of Medicine, Tampa, Florida.
Florida College · USUniversity of South Florida · USTampa General Hospital · US

Funding

Role of tubuloglomerular feedback in the development of hypertension in diabetesR01HL142814 · NHLBI · UNIVERSITY OF SOUTH FLORIDA · PI LIU, RUISHENG · 2019 to 2022
$2.4M
Renal hemodynamics and hypertension during pregnancyR01HL137987 · NHLBI · UNIVERSITY OF SOUTH FLORIDA · PI LIU, RUISHENG · 2018 to 2021
$1.6M
Primary cilia and modulation of the renal microcirculationR01DK099276 · NIDDK · UNIVERSITY OF SOUTH FLORIDA · PI LIU, RUISHENG · 2014 to 2017
$980k
NHLBI NIH HHS R01 HL137987NHLBI NIH HHS R01 HL142814NIDDK NIH HHS R01 DK099276
6 · The paper itself

Abstract

Transplanted kidneys usually experience several episodes of ischemia, including cold ischemia during allograft storage in preservation solution. However, previous studies focusing on cold renal ischemia were only carried out in vitro or ex vivo. In the present study, we developed and characterized an in vivo mouse model of renal ischemia-reperfusion injury (IRI) induced exclusively by cold ischemia. C57BL/6 mice underwent right kidney nephrectomy, and the left kidney was kept cool with circulating cold saline in a kidney cup, while body temperature was maintained at 37°C. We clamped the renal pedicle and flushed out the blood inside the kidney with cold saline via an opening on the renal vein. The severity of renal IRI was examined with different ischemic durations. We found that the mice with <2 h of cold ischemia exhibited no significant changes in renal function or histopathology; animals with 3 or 4 h of cold ischemia developed into mild to moderate acute kidney injury with characteristic features, including the elevation in plasma creatinine concentration and reduction in glomerular filtration rate and tubular necrosis, followed by a subsequent recovery. However, mice with 5 h of cold ischemia died in a few days with severe acute kidney injury. In summary, we generated a mouse model of renal IRI induced exclusively by cold ischemia, which mimics graft cold storage in preservation solution, and renal function can be evaluated in vivo.

Indexed as

Cold IschemiaKidney TransplantationAcute Kidney InjuryAnimalsAntigens, CDBiomarkersCadherin 5CadherinsCreatinineDisease Models, AnimalDisease ProgressionGlomerular Filtration RateKidneyMaleMice, Inbred C57BLNecrosisAntigens, CDBiomarkersCadherin 5CadherinsCreatininecold ischemiaischemia-reperfusion injurykidney transplantation

Identifiers

PMID31291121
PMCPMC6766631
OpenAlexW2956833392

What Socratic 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 Socratic graph.