Radioprotective Effect of Resveratrol for Early and Late Ionizing Radiation-Induced Damages on Colon and Rectum in Rats

dc.contributor.author Beceren, Ayfer
dc.contributor.author Aydemir, Sezgin
dc.contributor.author Atasoy, Beste Melek
dc.contributor.author Esin, A. K.
dc.contributor.author Ercan, Feriha
dc.contributor.author Sener, T. Emre
dc.contributor.author Sener, Goksel
dc.contributor.other Eczacılık Meslek Bilimleri Bölümü
dc.date.accessioned 2025-01-11T13:04:13Z
dc.date.available 2025-01-11T13:04:13Z
dc.date.issued 2023
dc.description.abstract Radiotherapy, which is routinely used to treat a wide range of oncological disorders, primarily affects the malignant tissue in the targeted area, but also have negative effects in the surrounding tissues. Pelvic radiotherapy causes early and late effects on the colon and rectum. Resveratrol (RVT) has been revealed to have a number of pharmacological effects in a variety of experimental models and clinical circumstances, therefore it has piqued the interest of scientists in recent years. In this study, we aimed to investigate the potential protective effects of resveratrol (RVT), a strong antioxidant, anti-inflammatory and anti-mutagenic agent, against toxicity of colonic and rectal tissues seen in the early and late stages after pelvic radiation. The treatment durations of the current study were designed as one week and ten weeks interval by following radiation exposure. Sprague Dawley rats were divided into 5 groups (8 animals/group) as the control, radiation-early effects (Rd-E), radiation-late effects (Rd-L), and RVT-treated Rd-E (Rd-E+RVT) and RVT-treated Rd-L (Rd-L+RVT) groups. Ionizing radiation was performed to the pelvic area that covers colon and rectum in single fraction of 20 Gy in a linear accelerator using with 6 MV photon energy. RVT was orally administered (10 mg/kg/day) immediately following the radiation exposure and continued daily for 1 and 10 weeks for early and late groups, respectively. Pelvic radiation caused a significant decrease in glutathione level, while malondialdehyde levels, myeloperoxidase activity and 8-hydroxydeoxyguanosine were increased in both Rd-E and Rd -L groups in the colon and rectum tissues. Additionally, light microscopic evaluations (H & E staining) revealed degeneration of epithelium and inflammatory cell infiltration in the colonic and rectal tissues in radiation groups. RVT treatment reversed all conducted biochemical parameters and ameliorated histomorphological changes following early and late effects of pelvic radiation in tissues. In conclusion, resveratrol may be a candidate as a radioprotector for normal tissues during and after radiotherapy. en_US
dc.identifier.citation 0
dc.identifier.doi 10.29228/jrp.446
dc.identifier.issn 2630-6344
dc.identifier.scopus 2-s2.0-85165925905
dc.identifier.uri https://doi.org/10.29228/jrp.446
dc.identifier.uri https://hdl.handle.net/20.500.14627/327
dc.language.iso en en_US
dc.publisher Marmara Univ en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Resveratrol en_US
dc.subject Early And Late Effect Of Radiation en_US
dc.subject Pelvic Radiation en_US
dc.subject Radioprotection en_US
dc.subject Oxidative Stress en_US
dc.subject 8-Ohdg en_US
dc.title Radioprotective Effect of Resveratrol for Early and Late Ionizing Radiation-Induced Damages on Colon and Rectum in Rats en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.institutional Şener, Göksel
gdc.author.scopusid 55342944300
gdc.author.scopusid 56452700400
gdc.author.scopusid 57202099921
gdc.author.scopusid 43261039200
gdc.author.scopusid 7006979286
gdc.author.scopusid 57216883630
gdc.author.scopusid 57216883630
gdc.author.wosid Aydemir, Sezgin/AAA-5858-2020
gdc.author.wosid Sener, Tarik/K-2501-2016
gdc.author.wosid Atasoy, Beste/AAG-9232-2021
gdc.description.department Fenerbahçe University en_US
gdc.description.departmenttemp [Beceren, Ayfer] Marmara Univ, Fac Pharm, Dept Toxicol, Istanbul, Turkiye; [Aydemir, Sezgin] Marmara Univ, Vocat Sch Hlth Serv, Dept Pathol Lab Technicianship, Istanbul, Turkiye; [Atasoy, Beste Melek] Marmara Univ, Sch Med, Dept Radiat Oncol, Istanbul, Turkiye; [Esin, A. K.] Marmara Univ, Fac Dent, Dept Histol & Embryol, Istanbul, Turkiye; [Ercan, Feriha] Marmara Univ, Sch Med, Dept Histol & Embryol, Istanbul, Turkiye; [Sener, T. Emre] Marmara Univ, Sch Med, Dept Urol, Istanbul, Turkiye; [Sener, Goksel] Fenerbahce Univ, Vocat Sch Hlth Serv, Istanbul, Turkiye en_US
gdc.description.endpage 1625 en_US
gdc.description.issue 4 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q4
gdc.description.startpage 1617 en_US
gdc.description.volume 27 en_US
gdc.description.woscitationindex Emerging Sources Citation Index
gdc.identifier.trdizinid 1190007
gdc.identifier.wos WOS:001037073200016
gdc.scopus.citedcount 0
gdc.wos.citedcount 0
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