Effect of the toll-like receptor 4 antagonist eritoran on retinochoroidal inflammatory damage in a rat model of endotoxin-induced inflammation
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info:eu-repo/semantics/openAccessTarih
2014Yazar
Ekici, FeyzahanKaraca, Emine Esra
Korkmaz, Şafak
Yüksel, Osman
Gülbahar, Özlem
Alper, Murat
Ercan, Sevim
Or, Meral
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Ekici, F., Karaca, E.E., Korkmaz, S., Yuksel, O., Gulbahar, O., Alper, M., Ercan, S., Or, M., (2014). Effect of the Toll-Like Receptor 4 Antagonist Eritoran on Retinochoroidal Inflammatory Damage in a Rat Model of Endotoxin-Induced Inflammation. Mediators of Inflammation, 2014. https://doi.org/10.1155/2014/643525Özet
Purpose. We investigated the effect of eritoran, a Toll-like receptor 4 antagonist, on retinochoroidal inflammatory damage in an endotoxin-induced inflammatory rat model. Methods. Endotoxin-induced inflammatory model was obtained by intraperitoneal injection of 1.5mg/kg lipopolysaccharide (LPS). Group 1 had control rats; in groups 2-3 LPS and 0.5mg/kg sterile saline were injected; and in groups 4-5 LPS and 0.5mg/kg eritoran were injected. Blood samples were taken and eyes were enucleated after 12 hours (h) (groups 2 and 4) or 24 hours (Groups 3 and 5). Tumor necrosis factor-alpha (TNF-alpha) and malondialdehyde (MDA) levels in the serum and retinochoroidal tissue and nuclear factor kappa-B (NF kappa B) levels in retinochoroidal tissue were determined. Histopathological examination was performed and retinochoroidal changes were scored. Results. Eritoran treatment resulted in lower levels of TNF-alpha, MDA, and NF kappa B after 12 h which became significant after 24 h. Serum TNF-alpha and retinochoroidal tissue NF kappa B levels were similar to control animals at the 24th h of the study. Eritoran significantly reversed histopathological damage after 24 h. Conclusions. Eritoran treatment resulted in less inflammatory damage in terms of serum and retinochoroidal tissue parameters.