Evidence map›Paper›PMID 25710927›Full record

ArticleExperimental biology and medicine (Maywood, N.J.)2015

Losartan reduces oxidative damage to renal DNA and conserves plasma antioxidant capacity in diabetic rats.

Maura Lodovici, Elisabetta Bigagli, Francesca Tarantini, Claudia Di Serio, Laura Raimondi

Open access · greenAbstract read
In one paragraph

Article in Experimental biology and medicine (Maywood, N.J.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

12 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Review
  3. Marine drugs · 2023
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  5. Article
  6. Article
  7. Review
  8. In vivo Assessment of Combined Effects of Glibenclamide and Losartan in Diabetic Rats.Medical principles and practice : international journal of the Kuwait University, Health Science Centre · 2019
    Article
  9. Article
  10. Article
  11. Article
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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 1 institution in 1 country.

Maura LodoviciDepartment of NEUROFARBA, Section of Pharmacology and Toxicology, University of Florence, 50139 Florence, Italy maura.lodovici@unifi.it.
Elisabetta BigagliDepartment of NEUROFARBA, Section of Pharmacology and Toxicology, University of Florence, 50139 Florence, Italy.
Francesca TarantiniDepartment of Experimental and Clinical Medicine, University of Florence, 50139 Florence, Italy.
Claudia Di SerioDepartment of Experimental and Clinical Medicine, University of Florence, 50139 Florence, Italy.
Laura RaimondiDepartment of NEUROFARBA, Section of Pharmacology and Toxicology, University of Florence, 50139 Florence, Italy.
University of Florence · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increased reactive oxygen species (ROS) levels produced by hyperglycemia and angiotensin-II (AT-II) are considered among the pathogenic factors in the malignant transformation of diabetic renal cells. We aimed to investigate the potential role of AT-II in the increased cancer risk seen in diabetes; measuring oxidative damage to renal DNA and protective antioxidant defenses, including adiponectin (Adp) and plasma antioxidant capacity by the Ferric Reducing Ability of Plasma (FRAP) method. In the kidney of streptozotocin (STZ)-induced (55 mg/kg) diabetic rats either treated or not treated for 3 weeks with losartan, an AT-II type 1 receptor antagonist (20 mg/kg/day); we measured 8-oxo-7,8-dihydro-2'-deoxyguanosine (8-oxodGuo) levels, as an index of oxidative DNA damage, circulating Adp and FRAP. Diabetic rats showed significantly higher 8-oxodGuo levels in renal DNA (8.48 ± 0.98 × 10(-6) dG, mean ± SEM n = 11) than normoglycemic ones (1.18 ± 0.04 × 10(-6) dG, mean ± SEM, n=7) and lower plasma Adp and FRAP levels in comparison to normoglycemics. The treatment of diabetic rats with losartan significantly (P < 0.01) reduced 8-oxodGuo levels (5.4 ± 0.58 × 10(-6) dG, mean ± SEM n=9) in renal DNA and conserved FRAP values. Moreover, an inverse correlation was found between 8-oxodGuo in kidney DNA and circulating Adp levels in normoglycemic and diabetic rats. Losartan treatment preserves FRAP levels, reduces DNA oxidative injury and thus the carcinogenesis risk. Furthermore, our results indicate that Adp plasma levels are a further marker of oxidative injury to the kidney and confirm that it is an important part of the plasma antioxidant defense.

Indexed as

DNA DamageOxidative Stress8-Hydroxy-2'-DeoxyguanosineAdiponectinAngiotensin II Type 1 Receptor BlockersAnimalsAntioxidantsDeoxyguanosineDiabetes Mellitus, ExperimentalDNAEnzyme-Linked Immunosorbent AssayHyperglycemiaKidneyLipidsLosartanMalondialdehyde8-Hydroxy-2'-DeoxyguanosineAdiponectinAngiotensin II Type 1 Receptor BlockersAntioxidantsDeoxyguanosineDNALipidsLosartanMalondialdehydeOxygenReactive Oxygen Species8-oxodGuoadiponectin (Adp)FRAPmalondialdehyde (MDA) losartanoxidative DNA damageSTZ-induced diabetes

Identifiers

PMID25710927
PMCPMC4935301
OpenAlexW2041617328

What OpenQuestion holds

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Registered trials

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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.