Evidence map›Paper›PMID 24550650›Full record

ArticleJournal of Korean medical science2014

Tempol attenuates renal fibrosis in mice with unilateral ureteral obstruction: the role of PI3K-Akt-FoxO3a signaling.

Hye Eun Yoon, Soo Jeong Kim, Sung Jun Kim, Sungjin Chung, Seok Joon Shin

Open access · goldAbstract read
In one paragraph

Article in Journal of Korean medical science, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

20 citing papers in PubMed, 41 citations in OpenAlex.

  1. Luteolin alleviates inflammation by inhibiting the PI3K-Akt-FOXO3a pathway.Naunyn-Schmiedeberg's archives of pharmacology · 2026
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  7. miR-122-5p Regulates Renal Fibrosis In Vivo.International journal of molecular sciences · 2022
    Article
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  12. Article
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  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Hydrogen Sulfide Donor GYY4137 Protects against Myocardial Fibrosis.Oxidative medicine and cellular longevity · 2015
    Article
  20. 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

5 authors at 2 institutions in 1 country.

Hye Eun YoonDepartment of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea. ; Division of Nephrology, Department of Internal Medicine, Incheon St. Mary's Hospital, Incheon, Korea.ORCID 0000-0002-6347-7282
Soo Jeong KimDepartment of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Sung Jun KimDepartment of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea. ; Division of Nephrology, Department of Internal Medicine, Incheon St. Mary's Hospital, Incheon, Korea.
Sungjin ChungDepartment of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Seok Joon ShinDepartment of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea. ; Division of Nephrology, Department of Internal Medicine, Incheon St. Mary's Hospital, Incheon, Korea.ORCID 0000-0001-7642-2849
The Catholic University of Korea Incheon St. Mary's Hospital · KRCatholic University of Korea · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study investigated whether tempol, an anti-oxidant, protects against renal injury by modulating phosphatidylinositol 3-kinase (PI3K)-Akt-Forkhead homeobox O (FoxO) signaling. Mice received unilateral ureteral obstruction (UUO) surgery with or without administration of tempol. We evaluated renal damage, oxidative stress and the expression of PI3K, Akt, FoxO3a and their target molecules including manganese superoxide dismutase (MnSOD), catalase, Bax, and Bcl-2 on day 3 and day 7 after UUO. Tubulointerstitial fibrosis, collagen deposition, α-smooth muscle actin-positive area, and F4/80-positive macrophage infiltration were significantly lower in tempol-treated mice compared with control mice. The expression of PI3K, phosphorylated Akt, and phosphorylated FoxO3a markedly decreased in tempol-treated mice compared with control mice. Tempol prominently increased the expressions of MnSOD and catalase, and decreased the production of hydrogen peroxide and lipid peroxidation in the obstructed kidneys. Significantly less apoptosis, a lower ratio of Bax to Bcl-2 expression and fewer apoptotic cells in TUNEL staining, and decreased expression of transforming growth factor-β1 were observed in the obstructed kidneys from tempol-treated mice compared with those from control mice. Tempol attenuates oxidative stress, inflammation, and fibrosis in the obstructed kidneys of UUO mice, and the modulation of PI3K-Akt-FoxO3a signaling may be involved in this pathogenesis.

Indexed as

AnimalsAntioxidantsCollagenCyclic N-OxidesFibrosisForkhead Box Protein O3Forkhead Transcription FactorsHydrogen PeroxideKidney DiseasesLipid PeroxidationMaleMiceMice, Inbred C57BLOxidative StressPhosphatidylinositol 3-KinasesPhosphorylationAntioxidantsCollagenCyclic N-OxidesForkhead Box Protein O3Forkhead Transcription FactorsFoxO3 protein, mouseHydrogen PeroxidePhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSpin LabelsSuperoxide DismutasetempolApoptosisFoxO3a Protein, MouseOxidative StressRenal FibrosisUnilateral Ureteral Obstruction

Identifiers

PMID24550650
PMCPMC3924002
OpenAlexW2107141257

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.