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dc.contributor.authorÖznam, Kadir
dc.contributor.authorŞirin, Duygu Yaşar
dc.contributor.authorYılmaz, İbrahim
dc.contributor.authorKaya, Yasin Emre
dc.contributor.authorİşyar, Mehmet
dc.contributor.authorGümüştaş, Seyit Ali
dc.contributor.authorÖzbek, Hanefi
dc.contributor.authorAkkaya, Semih
dc.contributor.authorKayhan, Arda
dc.contributor.authorMahiroğulları, Mahir
dc.date.accessioned10.07.201910:49:13
dc.date.accessioned2019-07-10T20:01:25Z
dc.date.available10.07.201910:49:13
dc.date.available2019-07-10T20:01:25Z
dc.date.issued2017en_US
dc.identifier.citationÖznam, K., Şirin, D. Y., Yılmaz, İ., Kaya, Y. E., İşyar, M., Gümüştaş, S. A. ... Mahiroğulları, M. (2017). Iopromide- and gadopentetic acid-derived preparates used in MR arthrography may be harmful to chondrocytes. Journal of Orthopaedic Surgery and Research, 12. https://dx.doi.org/10.1186/s13018-017-0600-5en_US
dc.identifier.issn1749-799X
dc.identifier.urihttps://dx.doi.org/10.1186/s13018-017-0600-5
dc.identifier.urihttps://hdl.handle.net/20.500.12511/3250
dc.descriptionWOS: 000405006500003en_US
dc.descriptionPubMed ID: 28651625en_US
dc.description.abstractBackground: Magnetic resonance arthrography, a procedure through which contrast agents containing gadolinium and/or iopromide are administered intra-articularly, has become a useful tool in musculoskeletal diagnosis. Nevertheless, despite being considered safe for systemic use, certain tissue toxicities have been identified for both drugs. In this study, the effects of short-term exposure of human primary chondrocyte cell cultures to gadolinium and/or iopromide contrast agents were examined by assaying for stage-specific embryonic antigen-1 (SSEA-1) protein expression (a chondrogenic differentiation marker), cell viability, toxicity, and proliferation. Methods: Human articular chondrocytes were grown in monolayer culture and were exposed to iopromide and/or gadolinium diethylenetriamine-pentaacetate (Gd-DPT) for 2 and 6 h. Cell cultures with no drug exposure were used as the control group. Cell differentiation status was assessed according to SSEA-1 protein expression. Contrast agent effects on cell viability and proliferation were analyzed using MTT analysis. Further, changes in cell morphology in relation to the control group were evaluated using inverted light microscopy, environmental scanning electron microscopy (ESEM), and 3-tesla magnetic resonance imaging. The obtained data were statistically compared. Results: When compared with the control group, both SSEA-1 protein expression and cell proliferation were lowest in the Gd-DPT group (P = 0.000). There was a statistically significant correlation between SSEA-1 expression and MTT results (rho = 0.351; P = 0.003). Conclusions: Nevertheless, the data obtained from in vitro experiments may not directly correspond to clinical applications. However, the mere fact that a drug used solely for diagnostic purposes may repress chondrocyte cell proliferation should be carefully considered by clinicians.en_US
dc.language.isoengen_US
dc.publisherBMCen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsCC0 1.0 Universal*
dc.rights.urihttps://creativecommons.org/publicdomain/zero/1.0/*
dc.subjectMR-Arthrographyen_US
dc.subjectGadopentetic Aciden_US
dc.subjectIopromideen_US
dc.subjectChondrotoxicityen_US
dc.subjectPrimary Cell Cultureen_US
dc.subjectStage-Specificen_US
dc.subjectEmbryonic Antigen-1en_US
dc.titleIopromide- and gadopentetic acid-derived preparates used in MR arthrography may be harmful to chondrocytesen_US
dc.typearticleen_US
dc.relation.ispartofJournal of Orthopaedic Surgery and Researchen_US
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü, Ortopedi ve Travmatoloji Ana Bilim Dalıen_US
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Tıbbi Farmakoloji Ana Bilim Dalıen_US
dc.authorid0000-0003-2003-6337en_US
dc.authorid0000-0002-8084-7855en_US
dc.identifier.volume12en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.1186/s13018-017-0600-5en_US
dc.identifier.wosqualityQ2en_US
dc.identifier.scopusqualityQ2en_US


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