Purpose: To evaluate the toxic effects of two triamcinolone acetonide (TA) vehicles on rabbit retina at different volumes. Methods: Vehicle A and B were prepared from two TA injections by centrifugation. Thirty-six New Zealand white rabbits were intravitreally injected with vehicle A, B, or balanced saline solution at 0.1 mL or 0.2 mL respectively. The eyes were examined by indirect ophthalmoscope, light microscope, and transmission electron microscope up to week 8 postinjection. Results: Eyes with vehicle A appeared normal under the ophthalmoscope, but showed disorganization in retinal inner nuclear layer and photoreceptor layer in pathologic analyses. Eyes with vehicle B displayed more significant retinal changes including retinal hemorrhage, vascular narrowing, myelinated fiber edema, retinal necrosis and atrophy, and photoreceptor apoptosis. There was an increase in degree of the above damages as the volume of either vehicle increased. Conclusion: Both vehicle A and B caused volume-related toxicity in rabbit retina. The intensity of the toxic effects of different vehicles may differ. Reducing or decanting the vehicles should be considered before intravitreal use of TA injections.
基金:
National Natural Science Foundation of China (No. 30571989).
第一作者机构:[1]Capital Med Univ, Beijing Tongren Eye Ctr, Beijing Tongren Hosp, Beijing 100730, Peoples R China
通讯作者:
推荐引用方式(GB/T 7714):
Li Qian,Wang Jingzhao,Yang Lin,et al.A morphologic study of retinal toxicity induced by triamcinolone acetonide vehicles in rabbit eyes[J].RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES.2008,28(3):504-510.doi:10.1097/IAE.0b013e318158e9c0.
APA:
Li, Qian,Wang, Jingzhao,Yang, Lin,Mo, Bin,Zeng, Huiyang...&Liu, Wu.(2008).A morphologic study of retinal toxicity induced by triamcinolone acetonide vehicles in rabbit eyes.RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES,28,(3)
MLA:
Li, Qian,et al."A morphologic study of retinal toxicity induced by triamcinolone acetonide vehicles in rabbit eyes".RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES 28..3(2008):504-510