dc.contributor.author | Oztekin, Cetin Volkan | |
dc.contributor.author | Yilmaz-Oral, Didem | |
dc.contributor.author | Kaya-Sezginer, Ecem | |
dc.contributor.author | Kirlangic, Omer Faruk | |
dc.contributor.author | Ozen, Fatma Zeynep | |
dc.contributor.author | Ozdal, Bulent | |
dc.contributor.author | Topcu, Hasan Onur | |
dc.date.accessioned | 2024-03-12T19:29:17Z | |
dc.date.available | 2024-03-12T19:29:17Z | |
dc.date.issued | 2021 | |
dc.identifier.issn | 1743-6095 | |
dc.identifier.issn | 1743-6109 | |
dc.identifier.uri | https://doi.org/10.1016/j.jsxm.2021.02.005 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12450/2255 | |
dc.description.abstract | Background: Effects of human umbilical cord blood (HUCB) as a valuable source for stem cell-based therapies have not been studied in persistent post-5-alpha reductase inhibitors (5ARI) erectile dysfunction (PPED). Aim: To determine the effect of intracavernosal injection of HUCB mononuclear cells (MNCs) on ED associated with dutasteride treatment. Methods: Twenty five adult male Sprague-Dawley rats were divided into 5 groups (n = 5 per group): (i) control, (ii) 8-week dutasteride (0.5 mg/kg/day, in drinking water), (iii) 12-week dutasteride, (iv) 8-week dutasteride+HUCB-MNCs (1 x 10(6)) and (v) 12-week dutasteride+HUCB-MNCs. HUCB-MNCs were administered intracavernosally after eight weeks of dutasteride treatment. Experiments were performed at 4 weeks following the injection of HUCB-MNCs. Erectile responses and isometric tension of corpus cavernosum (CC) were measured. The protein expressions of phosphodiesterase type 5 (PDE5), endothelial nitric oxide synthase (eNOS), neuronal NOS (nNOS), hypoxia-inducible factor (HIF)-1 alpha and smooth muscle/collagen contents in penile tissue were evaluated by Western blotting, immunohistochemistry, and Masson's trichrome staining, respectively. Main Outcome: In vivo erectile function, in vitro relaxant and contractile responses of CC, protein expression and localization of PDE5, eNOS, nNOS, HIF-1 alpha, and smooth muscle content in penile tissue. Results: Erectile responses in the dutasteride-treated groups were significantly decreased compared with controls (P < .001), persisting after 4-wk of washout. HUCB-MNCs restored diminished intracavernosal pressure responses, acetylcholine-, sodium nitroprusside-, sildenafil-induced relaxations, and increased phenylephrine and electrical field stimulation (EFS)-induced contractions. Decreased EFS-induced relaxations in dutasteride-treated groups were not restored by HUCB-MNCs. Increased PDE5 and reduced nNOS expressions in dutasteride groups were restored by HUCB-MNCs in the 12-week dutasteride group. eNOS and HIF-1 alpha protein expression and serum total and free testosterone levels were similar among groups. HUCB-MNCs reversed the decreased smooth muscle/collagen ratio in dutasteride-treated tissues. There was a significant increase in PDE5 and HIF-1 alpha staining in 8-week dutasteride animals. Clinical Translation: This study demonstrates the corrective potential of HUCB-MNCs on some persistent structural and functional deterioration caused by 5ARI treatment in rats, which may encourage further evaluation of HUCB-MNCs in men with PPED. Strengths and Limitations: Therapeutic application of intracavernosal HUCB-MNCs is a novel approach for the rat model of post-5ARI ED. Lack of serum and tissue dihydrotestosterone measurements, vehicle injections and characterization of the cells remain limitations of our study. Conclusion: The persistent ED after prolonged administration of dutasteride in rats is reversed by HUCB-MNC treatment, which holds promise as a realistic therapeutic modality for this type of ED. Copyright (C) 2021 International Society for Sexual Medicine. Published by Elsevier Inc. All rights reserved. | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Elsevier Sci Ltd | en_US |
dc.relation.ispartof | Journal Of Sexual Medicine | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | 5 Alpha Reductase Inhibitors | en_US |
dc.subject | Erectile Dysfunction | en_US |
dc.subject | Dutasteride | en_US |
dc.subject | Human Umbilical Cord Blood Stem Cell Transplantation | en_US |
dc.subject | Penis | en_US |
dc.title | Beneficial Effects of Human Umbilical Cord Blood Mononuclear Cells on Persistent Erectile Dysfunction After Treatment of 5-Alpha Reductase Inhibitor in Rats | en_US |
dc.type | article | en_US |
dc.department | Amasya Üniversitesi | en_US |
dc.authorid | Kaya-Sezginer, ecem/0000-0002-8490-6293 | |
dc.authorid | Yilmaz Oral, Didem/0000-0002-9515-0698 | |
dc.authorid | KIRLANGIÇ, Ömer Faruk/0000-0003-0219-3312; | |
dc.identifier.volume | 18 | en_US |
dc.identifier.issue | 5 | en_US |
dc.identifier.startpage | 889 | en_US |
dc.identifier.endpage | 899 | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.identifier.scopus | 2-s2.0-85105753638 | en_US |
dc.identifier.doi | 10.1016/j.jsxm.2021.02.005 | |
dc.department-temp | [Oztekin, Cetin Volkan] Univ Kyrenia, Dept Urol, Fac Med, Mersin, Turkey; [Yilmaz-Oral, Didem] Cukurova Univ, Dept Pharmacol, Fac Pharm, Adana, Turkey; [Kaya-Sezginer, Ecem; Gur, Serap] Ankara Univ, Dept Biochem & Pharmacol, Fac Pharm, Ankara, Turkey; [Kirlangic, Omer Faruk] Gazi Univ, Dept Med Biochem, Fac Med, Ankara, Turkey; [Ozen, Fatma Zeynep] Amasya Univ, Dept Pathol, Fac Med, Amasya, Turkey; [Ozdal, Bulent] Univ Hlth Sci, Ankara City Hosp, Dept Obstet & Gynecol, Ankara, Turkey; [Topcu, Hasan Onur] Mem Ankara Hosp, Dept Obstet & Gynecol, Ankara, Turkey; [Gur, Serap] Tulane Univ, Hlth Sci Ctr, Dept Urol, New Orleans, LA 70118 USA; [Gur, Serap] Tulane Univ, Hlth Sci Ctr, Dept Pharmacol, New Orleans, LA 70118 USA | en_US |
dc.identifier.wos | WOS:000651802200005 | en_US |
dc.identifier.pmid | 33785264 | en_US |
dc.authorwosid | Kaya-Sezginer, ecem/AAG-1498-2020 | |
dc.authorwosid | yilmaz oral, didem/GXV-6575-2022 | |
dc.authorwosid | KIRLANGIÇ, Ömer Faruk/AAB-4126-2021 | |
dc.authorwosid | Yilmaz Oral, Didem/J-9403-2018 | |
dc.authorwosid | Oztekin, Volkan/AAA-7639-2022 | |