Bitter Melon <i>(momordica Charantia)</I> Fruit Extract Ameliorates Methotrexate-Induced Reproductive Toxicity in Male Rats

dc.authorid Sener, Goksel/0000-0001-7444-6193
dc.authorid Ercan, Feriha/0000-0003-2339-5669
dc.authorid Cevik, Ozge/0000-0002-9325-3757
dc.authorid Kanpalta Mustafaoglu, Fatma/0000-0001-9832-6938
dc.authorid Sen, Ali/0000-0002-2144-5741
dc.authorwosid özbeyli, dilek/R-8421-2019
dc.authorwosid University, Aydin Adnan/Z-2790-2019
dc.authorwosid Ercan, Feriha/A-1655-2018
dc.authorwosid Cevik, Ozge/F-1326-2014
dc.contributor.author Şener, Göksel
dc.contributor.author Ozbeyli, Dilek
dc.contributor.author Sen, Ali
dc.contributor.author Cevik, Ozge
dc.contributor.author Sener, Goksel
dc.contributor.author Ercan, Feriha
dc.contributor.other Eczacılık Meslek Bilimleri Bölümü
dc.date.accessioned 2025-01-11T13:01:34Z
dc.date.available 2025-01-11T13:01:34Z
dc.date.issued 2021
dc.department Fenerbahçe University en_US
dc.department-temp [Kanpalta, Fatma; Ercan, Feriha] Marmara Univ, Sch Med, Dept Histol & Embryol, Istanbul, Turkey; [Ozbeyli, Dilek] Marmara Univ, Vocat Sch Hlth Sci, Pathol Lab Tech, Istanbul, Turkey; [Sen, Ali] Marmara Univ, Sch Pharm, Dept Pharmacognosy, Istanbul, Turkey; [Cevik, Ozge] Adnan Menderes Univ, Sch Med, Dept Biochem, Aydin, Turkey; [Sener, Goksel] Fenerbahce Univ, Vocat Sch Hlth Serv, Istanbul, Turkey en_US
dc.description Sener, Goksel/0000-0001-7444-6193; Ercan, Feriha/0000-0003-2339-5669; Cevik, Ozge/0000-0002-9325-3757; Kanpalta Mustafaoglu, Fatma/0000-0001-9832-6938; Sen, Ali/0000-0002-2144-5741 en_US
dc.description.abstract Objective: Methotrexate (MTX) is a drug commonly used for the treatment of malign neoplastic and inflammatory diseases. Anti-oxidant and anti-inflammatory effects of bitter melon (BM) were reported. The aim of this study was to examine the effects of BM fruit extract on MTX-induced testicular and epididymal damage. Materials and Methods: Sprague Dawley male rats were divided into three groups (n=8) as control, MTX and MTX+BM. A single dose of MTX (20 mg/kg) was injected intraperitoneally to the MTX and MTX+BM groups. BM fruit extract (600 mg/kg) was applied to the MTX+BM group orally for 5 days. Testes were examined for general histopathology, proliferating and apoptotic cells. The epididymis samples were used for the evaluation of sperm morphology. Oxidative and inflammatory markers were analysed biochemically. Results: Increased abnormal spermatozoa, degenerated seminiferous tubules with increased apoptotic cells and decreased proliferative cells were observed in the MTX group. TNF-alpha, IL-1 beta, 8-hydroxy-2-deoxyguanosine and caspase-3 levels increased, superoxide dismutase and catalase levels decreased in both testis and epididymis samples. All these histological and biochemical parameters were ameliorated in the MTX+BM group. Conclusion: Methotrexate causes testis damage by decreasing spermatogenic cells and increasing apoptosis through oxidative stress and inflammation. BM extract improves testis and epididymis damage with its possible anti-oxidant and anti-inflammatory effects. en_US
dc.description.woscitationindex Emerging Sources Citation Index
dc.identifier.citation 4
dc.identifier.doi 10.5472/marumj.988941
dc.identifier.endpage 228 en_US
dc.identifier.issn 1309-9469
dc.identifier.issue 3 en_US
dc.identifier.scopusquality Q4
dc.identifier.startpage 222 en_US
dc.identifier.uri https://doi.org/10.5472/marumj.988941
dc.identifier.uri https://hdl.handle.net/20.500.14627/147
dc.identifier.volume 34 en_US
dc.identifier.wos WOS:000715083000001
dc.language.iso en en_US
dc.publisher Marmara Univ, Fac Medicine en_US
dc.relation.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Methotrexate en_US
dc.subject Bitter Melon en_US
dc.subject Testis en_US
dc.subject Epididymis en_US
dc.subject Oxidative Stress en_US
dc.title Bitter Melon <i>(momordica Charantia)</I> Fruit Extract Ameliorates Methotrexate-Induced Reproductive Toxicity in Male Rats en_US
dc.type Article en_US
dc.wos.citedbyCount 4
dspace.entity.type Publication
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relation.isOrgUnitOfPublication.latestForDiscovery 5052e089-e75d-4aec-a280-6353973e4819

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