Evidence map›Paper›PMID 31168345›Full record

ArticleIranian journal of basic medical sciences2019

Therapeutic and protective effects of montelukast against doxorubicin-induced acute kidney damage in rats.

Evren Köse, Fatih Oğuz, Nigar Vardi, Mehmet Ediz Sarihan, Ali Beytur, Aytaç Yücel, Alaadin Polat, Nihat Eki Nci

Open access · greenAbstract read
In one paragraph

Article in Iranian journal of basic medical sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.6field-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

7 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. The renoprotective potential of montelukast: a scoping review.Annals of medicine and surgery (2012) · 2024
    Article
  3. Article
  4. Article
  5. Article
  6. Interference with megalin expression/endocytic function by montelukast mitigates gentamicin nephrotoxicity: Downregulation of ClC-5 expression.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2022
    Article
  7. Review
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 2 institutions in 1 country.

Evren KöseDepartment of Anatomy, School of Medicine, Inonu University, Malatya, Turkey.
Fatih OğuzDepartment of Urology, School of Medicine, Inonu University, Malatya, Turkey.
Nigar VardiDepartment of Histology-Embryology, School of Medicine, Inonu University, Malatya, Turkey.
Mehmet Ediz SarihanDepartment of Emergency, School of Medicine, Inonu University, Malatya, Turkey.
Ali BeyturDepartment of Urology, School of Medicine, Inonu University, Malatya, Turkey.
Aytaç YücelDepartment of Anesthesiology and Reanimation, School of Medicine, Inonu University, Malatya, Turkey.
Alaadin PolatDepartment of Physiology, School of Medicine, Inonu University, Malatya, Turkey.
Nihat Eki NciDepartment of Anatomy, School of Medicine, Erciyes University, Kayseri, Turkey.
Inonu University · TRErciyes University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe current study was designed to investigate the therapeutic and protective effects of montelukast (ML) against doxorubicin (DOX)-induced acute kidney damage in rats. MATERIALS AND

methodsThirty-five Wistar albino female rats were randomly divided into 5 groups as follows: Group I: Control; Group II: Control+ML; Group III: DOX; Group IV: DOX+ML; Group V: ML+DOX. At the end of the experiment, the kidney tissues of rats were collected. Thiobarbituric acid reactive substance (TBARS), reduced glutathione, superoxide dismutase (SOD), and catalase levels were determined from the kidney tissues. In addition, the kidney tissues were examined histologically.

resultsDOX induced a significant increase in the kidney TBARS levels, whereas SOD contents significantly decreased when compared with the control group. On the other hand, ML administration before and after DOX injection caused significant decreases in TBARS production and also increases in SOD levels. Histologically, the most remarkable damage was glomerulosclerosis and tubular changes in the DOX group. Moreover, marked tubular necrosis and swelling in tubular epithelial cells were observed in this group. Contrarily, although glomerulosclerosis was recognized as alleviated also in both DOX+ML and ML+DOX groups, the lesions did not completely ameliorate. However, treatment with ML after DOX injection was more effective than treatment with ML before DOX injection with respect to the protection of tubular structures.

conclusionIt was determined that ML treatment after DOX injection caused therapeutic effects against DOX-induced kidney damage. Thence, ML treatment is of some clinical properties for oxidative stress damage in kidney tissues.

Indexed as

DoxorubicinHistologyKidneyLeukotrienesOxidative stressTBARS

Identifiers

PMID31168345
PMCPMC6535195
OpenAlexW2921849545

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.