Effects of Intracameral Drugs and Dyes on Corneal Endothelial Cell Apoptosis in a Rat Model: An In Vivo and In Vitro Analysis

dc.contributor.authorBayar, Sezin Akca
dc.contributor.authorOzturker, Zeynep Kayaarasi
dc.contributor.authorAkova, Yonca Aydin
dc.contributor.authorBilezikci, Banu
dc.contributor.authorKarabay, Gulten
dc.contributor.orcID0000-0001-5109-755Xen_US
dc.contributor.pubmedID36578186en_US
dc.contributor.researcherIDAAJ-2406-2021en_US
dc.date.accessioned2023-09-13T10:09:45Z
dc.date.available2023-09-13T10:09:45Z
dc.date.issued2022
dc.description.abstractObjectives: To evaluate the effects of intracameral drugs and dyes on rat corneal endothelial apoptosis and cell morphology. Materials and Methods: The right eyes of 72 rats were injected intracamerally with 1% lidocaine, 0.01% adrenaline, triamcinolone acetonide (TA) 4 mg/mL, 1% trypan blue (TB), 0.5% indocyanine green (ICG), and fortified balanced salt solution as control. Corneal samples were taken 1 day and 1 week post-injection. Corneal endothelial apoptosis was assessed by the TUNEL technique, and the ratio of apoptotic cells in each group was compared with the control. Corneal endothelial cell morphology was evaluated in each specimen by transmission electron microscopy. Results: The mean apoptotic endothelial cell ratio was significantly higher at 1 day and 1 week after intracameral adrenaline injection when compared to controls (p=0.03 and 0.021, respectively). TB caused a significantly higher apoptotic cell ratio when compared to controls at 1 week after injection (p=0.043). Lidocaine caused a higher apoptotic cell ratio compared to TA and ICG at 1 week, although not statistically significant (p=0.058, 0.09, 0.69, respectively). In all experimental specimens, transmission electron microscopy showed morphological changes associated with apoptosis. Conclusion: This study showed that intracameral adrenaline, TB, and lidocaine injections may have toxic effects on corneal tissue, as indicated by ultrastructural and histopathological alterations. Therefore, these agents should be used with caution in intraocular surgery.en_US
dc.identifier.eissn2147-2661en_US
dc.identifier.endpage385en_US
dc.identifier.issn1300-0659en_US
dc.identifier.issue6en_US
dc.identifier.scopus2-s2.0-85145029212en_US
dc.identifier.startpage379en_US
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811223/pdf/TJO-52-379.pdf
dc.identifier.urihttp://hdl.handle.net/11727/10608
dc.identifier.volume52en_US
dc.identifier.wos000965672000004en_US
dc.language.isoengen_US
dc.relation.isversionof10.4274/tjo.galenos.2022.64369en_US
dc.relation.journalTURK OFTALMOLOJI DERGISI-TURKISH JOURNAL OF OPHTHALMOLOGYen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergien_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectIntracameral injectionen_US
dc.subjectcorneal endotheliumen_US
dc.subjectapoptosisen_US
dc.subjectTUNEL assayen_US
dc.subjectmorphologyen_US
dc.titleEffects of Intracameral Drugs and Dyes on Corneal Endothelial Cell Apoptosis in a Rat Model: An In Vivo and In Vitro Analysisen_US
dc.typearticleen_US

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