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AIM: To examine the protective effects and mechanism of adenovirally delivered pigment epithelium derived factor (Ad-PEDF) on experimental retinal ischemia reperfused injury (RIR) in rats. METHODS: RIR was induced in 96 adult rats by increasing intraocular pressure (IOP) via an intracameral infusion. All of the rats were divided into four groups: normal control group; RIR group; RIR + Ad-PEDF treatment group and RIR Ad-CMV control group. The groups were subdivided into groups of 12 hours, 24 hours, 72 hours and 168 hours after reperfusion randomly. The neuroprotective effects of Ad-PEDF were evaluated by determining the preservation of the inner retina thickness and the cell counts in the retinal ganglion cell layer by HE staining method. The levels of retinal ganglion cell (RGC) apoptosis were measured using the TdT-dUTP terminal nick-end labeling (TUNEL) method. RESULTS: Significant ameliorative effect on the thickness of the inner retina was observed in Ad-PEDF treated eyes. More cells in the RGC layer were retained in the Ad-PEDF treated eyes than untreated eyes. There were fewer apoptotic cells in the RGC layer in Ad-PEDF injected eyes than in untreated eyes. These results were statistically significant (P < 0.05, respectively). CONCLUSION: Intravitreal injection of Ad-PEDF protected the inner retina and the cells in the RGC layer of eyes after ischemia-reperfusion injury. Intravitreal injection of Ad-PEDF moderately protected rat retina from ischemia-reperfusion injury possibly by preventing apoptosis in retinal cells. LA: Chinese
Dr. X. Xu, Department of Ophthalmology, Hospital of China Medical University, Shenyang 110001 Liaoning Province, China. suxiexu73@sina.com
11.9 Gene therapy (Part of: 11 Medical treatment)
5.1 Rodent (Part of: 5 Experimental glaucoma; animal models)
11.8 Neuroprotection (Part of: 11 Medical treatment)