Please use this identifier to cite or link to this item:
https://hdl.handle.net/11499/47601
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Türkmen N.B. | - |
dc.contributor.author | Çiftçi O. | - |
dc.contributor.author | Taşlıdere A. | - |
dc.contributor.author | Aydın M. | - |
dc.contributor.author | Eke B.C. | - |
dc.date.accessioned | 2023-01-09T21:29:20Z | - |
dc.date.available | 2023-01-09T21:29:20Z | - |
dc.date.issued | 2022 | - |
dc.identifier.issn | 0303-4569 | - |
dc.identifier.uri | https://doi.org/10.1111/and.14557 | - |
dc.identifier.uri | https://hdl.handle.net/11499/47601 | - |
dc.description.abstract | Pembrolizumab is a monoclonal antibody. Anastrozole is an infertility inhibitor of aromatase. Resveratrol is an antioxidant polyphenol in the reproductive system. This study was planned to demonstrate the protective effects of anastrozole and resveratrol against pembrolizumab-induced reproductive damage. Forty-two Sprague–Dawley rats were used in the study. Groups: The control, Pembrolizumab (PEMB), PEMB + Anastrazol (ANAST), PEMB + Resveratrol (RES), RES, and ANAST groups. At the end of the experiment, rats were euthanased under anaesthesia. Tissue samples were taken from rats for biochemical, histological, and ELISA evaluations. Tissues were subjected to routine tissue follow-up for histological analysis. Biochemically, thiobarbituric acid reactive substance (TBARS), glutathione (GSH), catalase (CAT), superoxide dismutase (SOD), glutathione peroxidase (GSH-Px) levels were measured. Sperm motility, abnormal sperm rate, and epididymal sperm concentration were examined spermatologically. Serum testosterone and programmed cell death-1 (PD-1) levels were measured using the ELISA. TBARS levels were significantly increased and GSH, SOD, GPx, and CAT levels were mitigated in PEMB-treated rats. Histologically; Control, ANAST, and RES groups testis samples were observed with normal histological appearance. Histological damage was detected in seminiferous tubule structures in testicular tissue in the PEMB group. In treatment groups, this damage was decreased. In addition, PD-1 and testosterone levels were evaluated by the ELISA method. ANAST and RES have therapeutic effects against reproductive damage caused by PEMB. © 2022 Wiley-VCH GmbH. | en_US |
dc.language.iso | en | en_US |
dc.publisher | John Wiley and Sons Inc | en_US |
dc.relation.ispartof | Andrologia | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | anastrozole | en_US |
dc.subject | pembrolizumab | en_US |
dc.subject | resveratrol | en_US |
dc.subject | testis | en_US |
dc.subject | anastrozole | en_US |
dc.subject | catalase | en_US |
dc.subject | glutathione | en_US |
dc.subject | glutathione peroxidase | en_US |
dc.subject | pembrolizumab | en_US |
dc.subject | programmed death 1 receptor | en_US |
dc.subject | resveratrol | en_US |
dc.subject | superoxide dismutase | en_US |
dc.subject | testosterone | en_US |
dc.subject | anastrozole | en_US |
dc.subject | antioxidant | en_US |
dc.subject | aromatase | en_US |
dc.subject | aromatase inhibitor | en_US |
dc.subject | catalase | en_US |
dc.subject | glutathione | en_US |
dc.subject | glutathione peroxidase | en_US |
dc.subject | monoclonal antibody | en_US |
dc.subject | pembrolizumab | en_US |
dc.subject | polyphenol | en_US |
dc.subject | programmed death 1 receptor | en_US |
dc.subject | resveratrol | en_US |
dc.subject | superoxide dismutase | en_US |
dc.subject | testosterone | en_US |
dc.subject | thiobarbituric acid reactive substance | en_US |
dc.subject | adult | en_US |
dc.subject | animal cell | en_US |
dc.subject | animal experiment | en_US |
dc.subject | animal model | en_US |
dc.subject | animal tissue | en_US |
dc.subject | Article | en_US |
dc.subject | controlled study | en_US |
dc.subject | epididymis | en_US |
dc.subject | histology | en_US |
dc.subject | histopathology | en_US |
dc.subject | male | en_US |
dc.subject | nonhuman | en_US |
dc.subject | rat | en_US |
dc.subject | reproductive toxicity | en_US |
dc.subject | semen analysis | en_US |
dc.subject | seminiferous tubule | en_US |
dc.subject | sperm quality | en_US |
dc.subject | spermatozoon density | en_US |
dc.subject | spermatozoon motility | en_US |
dc.subject | testis disease | en_US |
dc.subject | testis tissue | en_US |
dc.subject | testis weight | en_US |
dc.subject | testosterone blood level | en_US |
dc.subject | therapy effect | en_US |
dc.subject | animal | en_US |
dc.subject | sperm | en_US |
dc.subject | Sprague Dawley rat | en_US |
dc.subject | testis | en_US |
dc.subject | Anastrozole | en_US |
dc.subject | Animals | en_US |
dc.subject | Antibodies, Monoclonal, Humanized | en_US |
dc.subject | Antioxidants | en_US |
dc.subject | Aromatase | en_US |
dc.subject | Aromatase Inhibitors | en_US |
dc.subject | Catalase | en_US |
dc.subject | Glutathione | en_US |
dc.subject | Glutathione Peroxidase | en_US |
dc.subject | Male | en_US |
dc.subject | Polyphenols | en_US |
dc.subject | Programmed Cell Death 1 Receptor | en_US |
dc.subject | Rats | en_US |
dc.subject | Rats, Sprague-Dawley | en_US |
dc.subject | Resveratrol | en_US |
dc.subject | Semen | en_US |
dc.subject | Sperm Motility | en_US |
dc.subject | Superoxide Dismutase | en_US |
dc.subject | Testis | en_US |
dc.subject | Testosterone | en_US |
dc.subject | Thiobarbituric Acid Reactive Substances | en_US |
dc.title | The effect of aromatase inhibitors against possible testis toxicity in pembrolizumab treated rats | en_US |
dc.type | Article | en_US |
dc.identifier.volume | 54 | en_US |
dc.identifier.issue | 10 | en_US |
dc.identifier.doi | 10.1111/and.14557 | - |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.authorscopusid | 57211524435 | - |
dc.authorscopusid | 27867577100 | - |
dc.authorscopusid | 57192546285 | - |
dc.authorscopusid | 7102765240 | - |
dc.authorscopusid | 57841483400 | - |
dc.identifier.pmid | 36177829 | en_US |
dc.identifier.scopus | 2-s2.0-85135850610 | en_US |
dc.identifier.wos | WOS:000851523600001 | en_US |
dc.identifier.scopusquality | Q2 | - |
item.languageiso639-1 | en | - |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
item.openairetype | Article | - |
item.cerifentitytype | Publications | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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