Evidence map›Paper›PMID 25428128›Full record

ArticleAmerican journal of physiology. Renal physiology2015

Oxidative stress contributes to orthopedic trauma-induced acute kidney injury in obese rats.

Peter N Mittwede, Lusha Xiang, Silu Lu, John S Clemmer, Robert L Hester

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

17 citing papers in PubMed, 26 citations in OpenAlex.

  1. Trial
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  3. Review
  4. Article
  5. Rodent models of AKI and AKI-CKD transition: an update in 2024.American journal of physiology. Renal physiology · 2024
    Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Early treatment with GLP-1 after severe trauma preserves renal function in obese Zucker rats.American journal of physiology. Regulatory, integrative and comparative physiology · 2019
    Article
  11. Carbon monoxide releasing molecule-2 protects mice against acute kidney injury through inhibition of ER stress.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2018
    Article
  12. Article
  13. Review
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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

5 authors at 2 institutions in 1 country.

Peter N MittwedeDepartment of Physiology and Biophysics, University of Mississippi Medical Center, Jackson, Mississippi.
Lusha XiangDepartment of Physiology and Biophysics, University of Mississippi Medical Center, Jackson, Mississippi.
Silu LuDepartment of Physiology and Biophysics, University of Mississippi Medical Center, Jackson, Mississippi.
John S ClemmerDepartment of Physiology and Biophysics, University of Mississippi Medical Center, Jackson, Mississippi.
Robert L HesterDepartment of Physiology and Biophysics, University of Mississippi Medical Center, Jackson, Mississippi Rhester@umc.edu.
University of Mississippi Medical Center · USJackson Memorial Hospital · US

Funding

STRUCTURAL VASCULAR ADAPTATION OF THE MICROCIRCULATIONP01HL051971 · NHLBI · UNIVERSITY OF MISSISSIPPI MEDICAL CENTER · PI HALL, JOHN E · 1993 to 2018
$39.4M
The role of leptin in autoimmune-associated hypertensionP20GM104357 · NIGMS · UNIVERSITY OF MISSISSIPPI MED CTR · PI TAYLOR, ERIN BASSFORD · 2013 to 2022
$23.4M
Microcirculation in Health and DiseaseR01HL089581 · NHLBI · UNIVERSITY OF MISSISSIPPI MED CTR · PI HESTER, ROBERT L · 2009 to 2012
$1.5M
NHLBI NIH HHS HL-51971NHLBI NIH HHS P01 HL051971NHLBI NIH HHS R01 HL089581NIGMS NIH HHS P20 GM104357NIGMS NIH HHS P20-GM-104357
6 · The paper itself

Abstract

After trauma, obese patients have an increased risk of developing acute kidney injury (AKI). We have demonstrated that obese Zucker (OZ) rats, but not lean Zucker (LZ) rats, develop AKI 24 h after orthopedic trauma. ROS have been implicated in the pathophysiology of AKI in models of critical illness. However, the contribution of ROS to trauma-induced AKI in the setting of obesity has not been determined. We hypothesized that AKI in OZ rats after trauma is mediated by increased oxidative stress. Male LZ and OZ rats were divided into control and trauma groups, with a subset receiving treatment after trauma with the antioxidant apocynin (50 mg/kg ip, 2 mM in drinking water). The day after trauma, glomerular filtration rate, plasma creatinine, urine kidney injury molecule-1, and albumin excretion as well as renal oxidant and antioxidant activity were measured. After trauma, compared with LZ rats, OZ rats exhibited a significant decrease in glomerular filtration rate along with significant increases in plasma creatinine and urine kidney injury molecule-1 and albumin excretion. Additionally, oxidative stress was significantly increased in OZ rats, as evidenced by increased renal NADPH oxidase activity and urine lipid peroxidation products (thiobarbituric acid-reactive substances), and OZ rats also had suppressed renal superoxide dismutase activity. Apocynin treatment significantly decreased oxidative stress and AKI in OZ rats but had minimal effects in LZ rats. These results suggest that ROS play an important role in AKI in OZ rats after traumatic injury and that ROS may be a potential future therapeutic target in the obese after trauma.

Indexed as

Oxidative StressAcute Kidney InjuryAlbuminuriaAnimalsBlood PressureBody WeightCell Adhesion MoleculesCreatinineFractures, BoneGlomerular Filtration RateMaleObesityRats, ZuckerReactive Oxygen SpeciesTumor Necrosis Factor-alphaCell Adhesion MoleculesCreatinineHavcr1 protein, ratReactive Oxygen SpeciesTumor Necrosis Factor-alphaacute kidney injuryinflammationobesityreactive oxygen speciestrauma

Identifiers

PMID25428128
PMCPMC4338927
OpenAlexW2083278532

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.