Evidence map›Paper›PMID 40943467›Full record

ArticleInternational journal of molecular sciences2025

Medical Ozone Treatment Attenuates Male Reproductive Toxicity Induced by Bleomycin, Etoposide, and Cisplatin Regimen in an Experimental Animal Model.

Necdet Altıner, Yaprak Dönmez Çakıl, İdil Duran, Damla Gökçeoğlu Kayalı, Hale Bayram, Abdullah Pehlivan, Oğuz Kaan Tombul, Belgin Selam, Mehmet Cıncık, Mustafa Erinç Sitar

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Necdet AltınerDepartment of Histology and Embryology, Faculty of Medicine, Maltepe University, 34858 Istanbul, Türkiye.ORCID 0000-0001-6837-068X
Yaprak Dönmez ÇakılDepartment of Medical Biology and Genetics, Faculty of Medicine, Maltepe University, 34858 Istanbul, Türkiye.ORCID 0000-0002-4605-1167
İdil DuranDepartment of Obstetrics and Gynecology, Faculty of Medicine, Maltepe University, 34858 Istanbul, Türkiye.ORCID 0000-0001-7818-491X
Damla Gökçeoğlu KayalıHistology and Embryology Department, Marmara University School of Medicine, 34854 Istanbul, Türkiye.ORCID 0000-0003-0674-090X
Hale BayramDepartment of Histology and Embryology, Faculty of Medicine, Maltepe University, 34858 Istanbul, Türkiye.ORCID 0000-0002-6104-8820
Abdullah PehlivanFaculty of Medicine, Maltepe University, 34857 Istanbul, Türkiye.ORCID 0009-0001-4419-5458
Oğuz Kaan TombulExperimental Animals Research and Application Center, Maltepe University, 34858 Istanbul, Türkiye.
Belgin SelamDepartment of Obstetrics and Gynecology, School of Medicine, Acibadem Mehmet Ali Aydinlar University, 34638 Istanbul, Türkiye.ORCID 0000-0003-4478-7514
Mehmet CıncıkDepartment of Histology and Embryology, Faculty of Medicine, Maltepe University, 34858 Istanbul, Türkiye.
Mustafa Erinç SitarExperimental Animals Research and Application Center, Maltepe University, 34858 Istanbul, Türkiye.

Funding

Scientific and Technological Research Council of Türkiye, Scientific Research Projects Unit of Maltepe University 123S891
6 · The paper itself

Abstract

The chemotherapeutic combination of bleomycin, etoposide, and cisplatin (BEP) is well-documented to exert gonadotoxic effects, ultimately leading to impaired fertility. This experimental rat study investigated the potential protective role of repeated medical ozone therapy in mitigating the deleterious effects of BEP treatment in male rats. Thirty-two adult male Sprague Dawley rats were randomly assigned to four groups: (i) a healthy control group, (ii) a group receiving injections of the BEP regimen over nine weeks, (iii) a group receiving the same BEP regimen plus medical ozone (1 mg/kg IP) twice weekly, and (iv) a group receiving only ozone therapy. BEP treatment significantly reduced sperm concentration and increased morphological abnormalities, both of which were partially restored by ozone co-administration. Ozone therapy also elevated testosterone and thyroid-stimulating hormone (TSH) levels when co-administered with BEP compared to BEP treatment alone. Oxidative stress analysis demonstrated that total oxidative status (TOS) and total antioxidant status (TAS) levels were significantly improved in the BEP + ozone group. Histopathological analysis revealed that ozone treatment ameliorated BEP-induced testicular damage, as evidenced by improved Johnsen scores and increased thickness of the seminiferous tubule epithelium. In conclusion, repeated medical ozone therapy appears to mitigate BEP-induced reproductive toxicity by preserving sperm quality, endocrine function, and redox homeostasis.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBleomycinCisplatinEtoposideOzoneReproductionAnimalsDisease Models, AnimalMaleOxidative StressRatsRats, Sprague-DawleySpermatozoaTestisBleomycinCisplatinEtoposideOzonebleomycincancerchemotherapycisplatinetoposideinfertilitymedical ozoneoxidative stressratsperm

Identifiers

PMID40943467
PMCPMC12428823

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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.