Evidence map›Paper›PMID 22707888›Full record

ArticleThe Korean journal of internal medicine2012

Phosphodiesterase inhibitor improves renal tubulointerstitial hypoxia of the diabetic rat kidney.

Hui-Kyoung Sun, Yun Mi Lee, Kum Hyun Han, Han-Seong Kim, Seon-Ho Ahn, Sang-Youb Han

Open access · goldAbstract read
In one paragraph

Article in The Korean journal of internal medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 17% 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, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Review
  6. Ferroptosis Enhanced Diabetic Renal Tubular InjuryFrontiers in endocrinology · 2021
    Article
  7. Review
  8. Evolving spectrum of diabetic nephropathy.World journal of diabetes · 2019
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Effects and clinical significance of pentoxifylline on the oxidative stress of rats with diabetic nephropathy.Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban · 2015
    Article
  14. Article
  15. Article
  16. Article
  17. Effect of phosphodiesterase inhibitor on diabetic nephropathy.The Korean journal of internal medicine · 2012
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Hui-Kyoung SunDivision of Nephrology, Department of Internal Medicine, Ilsan-Paik Hospital, Inje University College of Medicine, Goyang, Korea.
Yun Mi Lee
Kum Hyun Han
Han-Seong Kim
Seon-Ho Ahn
Sang-Youb Han
Inje University Ilsan Paik Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimsRenal hypoxia is involved in the pathogenesis of diabetic nephropathy. Pentoxifyllin (PTX), a nonselective phosphodiesterase inhibitor, is used to attenuate peripheral vascular diseases. To determine whether PTX can improve renal hypoxia, we investigated its effect in the streptozocin (STZ)-induced diabetic kidney.

methodsPTX (40 mg/kg, p.o.) was administered to STZ-induced diabetic rats for 8 weeks. To determine tissue hypoxia, we examined hypoxic inducible factor-1α (HIF-1α), heme oxygenase-1 (HO-1), vascular endothelial growth factor (VEGF), and glucose transporter-1 (GLUT-1) levels. We also tested the effect of PTX on HIF-1α in renal tubule cells.

resultsPTX reduced the increased protein creatinine ratio in diabetic rats at 8 weeks. HIF-1α, VEGF, and GLUT-1 mRNA expression increased significantly, and the expression of HO-1 also tended to increase in diabetic rats. PTX significantly decreased mRNA expression of HIF-1α and VEGF at 4 and 8 weeks, and decreased HO-1 and GLUT-1 at 4 weeks. The expression of HIF-1α protein was significantly increased at 4 and 8 weeks in tubules in the diabetic rat kidney. PTX tended to decrease HIF-1α protein expression at 8 weeks. To examine whether PTX had a direct effect on renal tubules, normal rat kidney cells were stimulated with CoCl(2) (100 µM), which enhanced HIF-1α mRNA and protein levels under low glucose conditions (5.5 mM). Their expressions were similar even after high glucose (30 mM) treatment. PTX had no effect on HIF-1α expression.

conclusionsPTX attenuates tubular hypoxia in the diabetic kidney.

Indexed as

AnimalsCell LineCobaltDiabetes Mellitus, ExperimentalDiabetic NephropathiesDisease Models, AnimalGene Expression RegulationGlucoseGlucose Transporter Type 1Heme Oxygenase (Decyclizing)HypoxiaHypoxia-Inducible Factor 1, alpha SubunitKidney TubulesMalePentoxifyllinePhosphodiesterase InhibitorsCobaltcobaltous chlorideGlucoseGlucose Transporter Type 1Heme Oxygenase (Decyclizing)Hif1a protein, ratHmox1 protein, ratHypoxia-Inducible Factor 1, alpha SubunitPentoxifyllinePhosphodiesterase InhibitorsRNA, MessengerSlc2a1 protein, ratStreptozocinVascular Endothelial Growth Factor Avascular endothelial growth factor A, ratCell hypoxiaDiabetic nephropathiesPhosphodiesterase inhibitors

Identifiers

PMID22707888
PMCPMC3372800
OpenAlexW2038510488

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.