Endothelium, Corneal

PURPOSE: To evaluate the endothelial function of cornea preserved in newly developing korean corneal storage media (CS002, CS003) by estimating the permeability of corneal endothelium and the change of corneal thickness. METHODS: The cornea were divided into six experimental groups - fresh group immediately after enucleation, 4degrees Cmoist chamber group preserved for 24 hours and 48 hours, Optisol & CS002 group for 1, 3, 5, and 7 days, and Likorol & CS003 group for 7, 10, and 14 days after enucleation, and then corneal endothelial permeability(Pac) was measured using carboxyfluorescein solution. Corneal thickness was measured using pachymeter(fine focus adjustment) of the specular microscope. RESULTS: Corneal endothelial Pac (x1 0(- 4) cm/min) was 3.64+/-0.33 in fresh group, 4.79+/-0.28 in 4degrees Cmoist chamber group for 24 hours. Each endothelial Pac of CS002 group at 5 and 7 days was 5.81+/-0.55 and 5.65+/-0.58, which were different with 4degrees Cmoist chamber preservation group for 24 hours(p<0.05) but not different with Optisol groups at same days. Each endothelial Pac of CS003 group at 7, 10, and 14 days was 4.34+/-0.34, 4.66+/-0.59, and 4.66+/-0.27, which were not different from those of Likorol. Each corneal thickness of CS002 and Optisol group at 7days was 417.80+/-19.37 mu m and 421.00+/-19.75mu m, which were resemble increment. Corneal thickness was 426.75+/-22.43mu m in CS003 group and 476.00+/- 40.08mu m in Likorol group at 7days. There was statistical difference between the two group(P<0.05), and this difference was sustained for 14days (P<0.05). CONCLUSION: There was no difference in the effect on corneal endothelial permeability between korean corneal storage media such as CS002 and CS003, and that of previous corneal storage media such as Optisol and Likorol. Corneal thickness of cornea preserved in korean corneal storage media was thinner than that of Likorol.
Cornea* ; Endothelium, Corneal ; Permeability

No Abstract Available.
Animals ; Cats* ; Endothelium, Corneal*

No Abstract Available.
Endothelium, Corneal* ; Lidocaine*

Objective: To determine the safety of intracamerally injected preservative-free 0.5% moxifloxacin/0.1% dexamethasone fixed-dose combination on the corneal endothelium in a rabbit model and compare it to intracamerally injected preservative-free 0.5% moxifloxacin. Methods: This experimental study included twenty eyes from ten albino rabbits. The eyes were assessed for baseline corneal clarity and anterior chamber (AC) inflammation using slit-lamp biomicroscopy. A specular microscope measured the corneal endothelial cell density (ECC) and corneal thickness (CT). Intracameral injections of 0.1 mL 0.5% moxifloxacin ophthalmic solution were administered to the 10 right eyes (IPFM group) and 0.1 mL of 0.5% moxifloxacin/0.1% dexamethasone fixed-dose preparation were administered to the 10 left eyes (IPFMDex group). In both groups, ECC, CT, corneal clarity, and AC inflammation at Day 1 (one day post-injection) and Day 7 (seven days post-injection) were compared with Day 0 (baseline). The IPFMDex group was also compared with the IPFM group at Days 0, 1, and 7. The endothelial cells of harvested corneas from both groups at Day 1 and 7 were stained with trypan blue and alizarin red, and compared for endothelial cell damage (ECD). Data were analyzed using paired and independent sample t-tests. Results: In both the IPFM and IPFMDex groups, ECC and CT at Day 1 (IPFM: ECC p=0.07, CT p=0.76; IPFMDex: ECC p=0.41, CT p=0.94) and Day 7 (IPFM: ECC p=0.95, CT p=0.28; IPFMDex: ECC p=0.29, CT p=0.34) were not different from Day 0 (baseline). No significant difference in ECC, CT, and ECD were found between the IPFM and IPFMDex groups at Day 1 (ECC p=0.82, CT p=0.36, ECD p=0.96) and Day 7 (ECC p=0.95, CT p=0.22, ECD p=0.61). Throughout the study, the cornea in both groups were clear and showed no signs of AC inflammation. Conclusion Intracameral injection of preservative-free moxifloxacin/dexamethasone fixed-dose formulation was safe on the rabbit corneal endothelium and was no different from preservative-free moxifloxacin.
Moxifloxacin ; Dexamethasone ; Endothelium, Corneal

In order to interprete the significance of the vacuolation found in the corneal endothelium, flat preparations of the corneal endothelium were made in human eyes aged from neonate to 72 year. The result were as follows. 1. The endothelial vacuoles were more frequent with the increase in the time of the post-mortem delay. 2. The endothelial vacuoles were more prevalent in aged. 3. The vacuoles in the endothelium were more easily formed in the peripheral area than the central area. 4. Gross vacuolation found in the corneal endothelium was shown to be the result of post mortem degeneration.
Endothelium ; Endothelium, Corneal* ; Humans ; Infant, Newborn ; Vacuoles*

Keratic precipitates are deposits of material on the posterior surface of the cornea, which is a relatively common phenomenon in a variety of circumstances both physiological and pathological. Inflammatory cells and uveal pigment in the aqueous show a strong tendency to adhere to one another and to the corneal endothelium, thus forming fine or large deposits. We observed the several kinds of keratic precipitates on the corneal endothelium by flat preoparation method. The character of the keratic precipitates observed in this study was composed of inflammatory cells, erythrocyte, pigment granules derived from the breakdown of red blood cells. In view of the accumulation of the pigment granules into the cytoplasm, it seemed that the endothelium might participate in phagocytosis or secondary changes in the various corneal disease.
Cornea ; Corneal Diseases ; Cytoplasm ; Endothelium ; Endothelium, Corneal ; Erythrocytes ; Phagocytosis

PURPOSE: To analyze the features of corneal tissue in patients with posterior polymorphous corneal dystrophy (PPMD) using in vivo confocal microscopy (IVCM). CASE SUMMARY: Three patients with clinically diagnosed PPMD were examined using IVCM. Cross-sectioned corneal images of the corneal epithelium, Bowman's layer, stromal layer, Descemet's membrane, and endothelium were evaluated. IVCM demonstrated a depressed crater-like lesion, hyper-dense streak-like lesion, and surface irregularity of the corneal endothelium. Endothelial hypo-reflective vesicular and band-like lesions were also found. Pleomorphism and polymegathism were present with guttae and hyper-reflective endothelial nuclei. CONCLUSIONS: IVCM is a non-invasive and effective tool to diagnose PPMD.
Corneal Dystrophies, Hereditary ; Descemet Membrane ; Endothelium ; Endothelium, Corneal ; Epithelium, Corneal ; Humans ; Microscopy, Confocal

In this immunohistochemical study we applied a monoclonal antibody(mAb) to evaluate the expression pattern of lymphocyte functionassociated antigen 3(LFA-3) in rabbit`s corneas before and after intracorneal injection of Candida albicans. Ten right eyes were induced to get immunocompromized cornea with subconjunctival injection of 2mg of dexamethasone once a day for 3 days(group I), and 10 left eyes had normal cornea without subconjunctival injection of dexamethazone(group II). Each 2 corneas in both group I and II were resected at 3, 12, 24 and 72 hours after intracorneal injection of C. albicans. Each 2 corneas without intracorneal injection of C. albicans in both groups were used as a control. The results were as follows: LFA-3 was expressed weakly on corneal epithlium in control of group I and group II. Expression of LFA-3 on vascular endothelium of group II was somewhat stronger than that of group I, LFA-3 was expressed moderately on vascular endothelium, and was detected on corneal stroma at 3 hors after intracorneal injection in both groups. Expression of LFA-3 on corneal stroma was slightly increased in both group II, and markedly increased in group I at 12 hours after intracorneal injection. Group II showed slightly increased LFA-3 expression on corneal and II to be expressed on corneal endothelium and inflammatory cells at 24 hours after injection. Its expression on corneal epithelium, stroma and endothelium was more increased in group II than in group I at that time. Group I showed moderate LFA-3 expression on corneal epithelium, corneal endothelium and inflammatory cells, and strong expression on corneal stroma and vascular endothelium at 72 hours after infection. Otherwise, LFA-3 expression in group II was weak to moderate n corneal epithelium, corneal endothelium and inflammatory cell, and moderate on corneal stroma and vascular endothelium. In this study, it was found that expression of LFA-3 in group I was weaker than that in group II in control and at 3 hours after intracorneal injection of C. albicans, but group I showed more strong LFA-3 expression than group II after 12 hours of intracorneal injection.
Antigens, CD58 ; Candida albicans* ; Candida* ; Cornea ; Corneal Stroma ; Dexamethasone ; Endothelium ; Endothelium, Corneal ; Endothelium, Vascular ; Epithelium, Corneal ; Lymphocytes ; Rabbits*

It has been reported that ascorbic acid[AA]appears to be actively taken up by the corneal endothelium and protect the endothelium against harmful effects of the oxidative reactions. To investigate the effect of ascorbic acidon the corneal endothelial function, rabbit`s corneas were mounted in the in vitro specular microscope. Corneal endothelium was perfused with ascorbic acid, then switched to AA plus ouabain solution, and vice versa. Also, phloretin was perfused onto the endothelium with AA and ouabain. Andcorneal endothelium was perfused with GBR or AA solution followed by perfusion with ouabain. Corneal thickness was measured during the perfusion and the corneal swelling rate calculated. Corneal endothelial permeability was also measured after perfusion of ascorbic acid. Perfusion with AA showed no corneal swelling, but swelling rate was even lower than GBR control. Corneal endothelial permeability did not change upon AA perfusion. In corneas preperfused with ouabain, AA added to ouabain solution decreased corneal swelling rates induced by ouabain solution[19.9 vs. 40.5 micrometer/hr]. The corneas preperfused with AA also showed decreased swelling rates with subsequent perfusion of ouabain added to AA solution[21.7 vs.28.6 micrometer/ hr]. Phloretin inhibited the effect of AA.However, when ouabain was removed, the corneal swelling plateaued but did not return to baseline thickness in both AA and GBR perfusion.The results of this study showed that AA can increase corneal endothelial pump function and reduce corneal swelling caused by ouabain.
Ascorbic Acid* ; Cornea ; Endothelium ; Endothelium, Corneal ; Ouabain ; Perfusion ; Permeability ; Phloretin