Evidence map›Paper›PMID 38564077›Full record

ArticleInternational urology and nephrology2024

Standardizing urethral stricture models in rats: a comprehensive study on histomorphologic and molecular approach.

Osman Ergün, Muhammet Yusuf Tepebaşi, İbrahim Onaran, Sefa Alperen Öztürk, Mücahit Baltik, Pinar Aslan Koşar

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Article in International urology and nephrology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 26% 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

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 2 citations in OpenAlex.

  1. Pooled it
  2. 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

6 authors at 1 institution in 1 country.

Osman ErgünMedical Faculty, Department of Urology, Süleyman Demirel University, Akademik Kat Sekreterliği, Doğu yerleşkesi, Çünür, Isparta, Turkey. osmanergun77@gmail.com.ORCID http://orcid.org/0000-0001-7611-0933
Muhammet Yusuf TepebaşiMedical Faculty, Department of Medical Genetic, Süleyman Demirel University, Isparta, Turkey.ORCID http://orcid.org/0000-0002-1087-4874
İbrahim OnaranMedical Faculty, Department of Medical Biology, Süleyman Demirel University, Isparta, Turkey.ORCID http://orcid.org/0000-0002-2524-0233
Sefa Alperen ÖztürkMedical Faculty, Department of Urology, Süleyman Demirel University, Akademik Kat Sekreterliği, Doğu yerleşkesi, Çünür, Isparta, Turkey.ORCID http://orcid.org/0000-0003-4586-9298
Mücahit BaltikDepartment of Urology, Malazgirt State Hospital, Muş, Turkey.ORCID http://orcid.org/0009-0006-2692-0544
Pinar Aslan KoşarMedical Faculty, Department of Medical Biology, Süleyman Demirel University, Isparta, Turkey.ORCID http://orcid.org/0000-0003-2602-5145
Süleyman Demirel University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo create a reproducible and standardized urethral stricture model in rats, evaluating both histomorphologic findings and gene expression data. In studies involving experimental animals, more standardization is needed for the creation of a urethral stricture model.

methodsSixteen male rats were randomized into two groups. The Sham group (n:8) underwent only a penoscrotal incision, while the stricture group (n:8) had their urethras exposed through a penoscrotal incision, followed by electrocauterization to the corpus spongiosum. On the 15th day, blood and urethral tissues were harvested for histologic and molecular analyses. Histomorphologic, immunohistochemical, and reverse transcription polymerase chain reaction analyses were performed.

resultsThe stricture group exhibited more severe and intense spongiofibrosis, inflammation, epithelial desquamation, and congestion in vascular structures compared to the controls (p < 0.05). The urethral tissue in the stricture group showed an increased ratio of inflammation parameters, including Collagen 1A1, Collagen 3A1, elastin, Transforming growth factor β1, α Smooth muscle actin, Platelet-derived growth factor α, and Platelet-derived growth factor β. Transforming growth factor β1, Platelet-derived growth factor α, and Platelet-derived growth factor β each correlated highly with the other six parameters (r > 0.60, p < 0.05).

conclusionDeveloping electrocoagulation-induced urethral stricture in rats is a simple, reliable, inexpensive, and reproducible. Reporting histologic data with qualitative and semi-quantitative scoring will enhance data standardization, aiding reader understanding and analysis. Transforming growth factor β and Platelet-derived growth factor play key roles in fibrosis during stricture development. Incorporating these cytokines in urethral stricture animal model studies can demonstrate successful stenosis creation.

Indexed as

Disease Models, AnimalFibrosisUrethraUrethral StrictureActinsAnimalsCollagen Type ICollagen Type I, alpha 1 ChainCollagen Type IIIElastinElectrocoagulationMalePlatelet-Derived Growth FactorRandom AllocationRatsRats, Sprague-DawleyActa2 protein, ratActinsCOL3A1 protein, ratCollagen Type ICollagen Type I, alpha 1 ChainCollagen Type IIIElastinPlatelet-Derived Growth FactorTgfb1 protein, ratTransforming Growth Factor beta1CytokinesElectrocoagulationPlatelet derivetad growth factorRatTransforming growth factor β 1Urethral stricture

Identifiers

PMID38564077
OpenAlexW4393431287

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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.