Bitter Melon (Momordica charantia) Fruit Extract Ameliorates Methotrexate-Induced Reproductive Toxicity in Male Rats

dc.contributor.author Kanpalta, Fatma
dc.contributor.author Özbeyli, Dilek
dc.contributor.author Sen, Ali
dc.contributor.author Cevik, O. Dağdeviren
dc.contributor.author Şener, Göksel
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.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-α, IL-1β, 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. © 2025 Elsevier B.V., All rights reserved. en_US
dc.identifier.citation 4
dc.identifier.doi 10.5472/marumj.988941
dc.identifier.issn 1019-1941
dc.identifier.issn 1309-9469
dc.identifier.scopus 2-s2.0-105012388635
dc.identifier.uri https://doi.org/10.5472/marumj.988941
dc.language.iso en en_US
dc.publisher Marmara University en_US
dc.relation.ispartof Marmara Medical Journal en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Bitter Melon en_US
dc.subject Epididymis en_US
dc.subject Methotrexate en_US
dc.subject Oxidative Stress en_US
dc.subject Testis en_US
dc.title Bitter Melon (Momordica charantia) Fruit Extract Ameliorates Methotrexate-Induced Reproductive Toxicity in Male Rats en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id Sener, Goksel/0000-0001-7444-6193
gdc.author.id Ercan, Feriha/0000-0003-2339-5669
gdc.author.id Cevik, Ozge/0000-0002-9325-3757
gdc.author.id Kanpalta Mustafaoglu, Fatma/0000-0001-9832-6938
gdc.author.id Sen, Ali/0000-0002-2144-5741
gdc.author.institutional Şener, Göksel
gdc.author.scopusid 57807056400
gdc.author.scopusid 6504603410
gdc.author.scopusid 55250649800
gdc.author.scopusid 24400636500
gdc.author.scopusid 55662834600
gdc.author.scopusid 7006979286
gdc.description.department Fenerbahçe University en_US
gdc.description.departmenttemp [Kanpalta] Fatma, Department of Histology and Embryology, Marmara Üniversitesi Tip Fakültesi, Istanbul, Turkey; [Özbeyli] Dilek, Pathology Laboratory, Marmara Üniversitesi, Istanbul, Turkey; [Sen] Ali, Department of Pharmacognosy, Marmara Üniversitesi, Istanbul, Turkey; [Cevik] O. Dağdeviren, Department of Biochemistry, Aydin Adnan Menderes University, Aydin, Turkey; [Şener] Göksel, Vocational School of Health Services, Fenerbahçe University, Istanbul, Turkey; [Ercan] Feríha, Department of Histology and Embryology, Marmara Üniversitesi Tip Fakültesi, Istanbul, Turkey en_US
gdc.description.endpage 228 en_US
gdc.description.issue 3 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q4
gdc.description.startpage 222 en_US
gdc.description.volume 34 en_US
gdc.description.woscitationindex Emerging Sources Citation Index
gdc.description.wosquality N/A
gdc.identifier.wos WOS:000715083000001
gdc.wos.citedcount 4
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