Comparación de tres métodos de inducción del incremento crónico de la presión intraocular en el cerdo (glaucoma experimental)
ISSN: 0365-6691
Année de publication: 2005
Volumen: 80
Número: 10
Pages: 571-579
Type: Article
D'autres publications dans: Archivos de la Sociedad Española de Oftalmologia
Résumé
Purpose: To compare three methods of inducing experimental glaucoma in the adult pig, based on achieving chronic elevation of the intraocular pressure (IOP). Methods: A total of 16 adult pigs were used in the present study. In all instances, the right eye was used as control and the left eye as the experimental eye. The animals were divided into three groups: 1) 3 pigs in which 3 episcleral veins were cauterized (experimental period = 21 weeks); 2) 6 animals in which the anterior chamber of the eye was injected with a solution containing latex fluorospheres (experimental period = 11 weeks); and 3) 4 pigs in which the anterior chamber of the eye was injected with a solution containing latex fluorospheres plus methylcellulose (experimental period = 11 weeks). Results: The episcleral vein cauterization was the only method which produced a sustained elevation of the IOP throughout most of the experimental period. Moreover, the elevation of the IOP achieved by this method resulted in selective retinal ganglion cell (RGC) loss that affected mainly the mid-peripheral and peripheral retina and caused an increase in the mean soma area of the remaining RGCs. Conclusions: Cauterization of the episcleral veins resulted in a significant and sustained elevation of the IOP and RGC loss when compared with the other two approaches tested in the present study, which barely modified the pig's RGC distribution. Thus, we conclude that the episcleral vein cauterization is the best of the methods tested to induce experimental glaucoma in the pig.
Références bibliographiques
- Muller, B, Boeck, T, Hartmann, C. (2004). Effect of excimer laser beam delivery and beam shaping on corneal sphericity in photorefractive keratectomy. J Cataract Refract Surg. 30. 464-470
- Li, ZY, Wong, F, Chang, JH, Possin, DE, Hao, Y, Petters, RM. (1998). Rhodopsin transgenic pigs as a model for human retinitis pigmentosa. Invest Ophthalmol Vis Sci. 39. 808-819
- Prince, JH, Diesem, CD, Eglitis, I, Ruskell, GL. (1960). The pig. Charles C Thomas Publisher. Springfield.
- Beauchemin, ML. (1974). The fine structure of the pig´s retina. Albrecht Von Graefes Arch Klin Exp Ophthalmol. 190. 27-45
- McMenamin, PG, Steptoe, RJ. (1991). Normal anatomy of the aqueous humour outflow system in the domestic pig eye. J Anat. 178. 65-77
- Olsen, TW, Sanderson, S, Feng, X, Hubbard, WC. (2002). Porcine sclera: thickness and surface area. Invest Ophthalmol Vis Sci. 43. 2529-2532
- Hendrickson, A, Hicks, D. (2002). Distribution and density of medium- and short-wavelength selective cones in the domestic pig retina. Exp Eye Res. 74. 435-444
- Ruiz-Ederra, J, Hitchcock, PF, Vecino, E. (2003). Two classes of astrocytes in the adult human and pig retina in terms of their expression of high affinity NGF receptor (TrkA). Neurosci Lett. 337. 127-130
- Ruiz-Ederra, J, Garcia, M, Hicks, D, Vecino, E. (2004). Comparative study of the three neurofilament subunits within pig and human retinal ganglion cells. Mol Vis. 10. 83-92
- García, M, Ruiz-Ederra, J, Hernandez-Barbachano, H, Vecino, E. (2005). Topography of pig retinal ganglion cells. J Comp Neurol. 486. 361-372
- Glovinsky, Y, Quigley, HA, Pease, ME. (1993). Foveal ganglion cell loss is size dependent in experimental glaucoma. Invest Ophthalmol Vis Sci. 34. 395-400
- Vickers, JC, Schumer, RA, Podos, SM, Wang, RF, Riederer, BM, Morrison, JH. (1995). Differential vulnerability of neurochemically identified subpopulations of retinal neuron in a monkey model of glaucoma. Brain Res. 680. 23-35
- Shou, T, Liu, J, Wang, W, Zhou, Y, Zhao, K. (2003). Differential dendritic shrinkage of alpha and beta retinal ganglion cells in cats with chronic glaucoma. Invest Ophthalmol Vis Sci. 44. 3005-3010
- Quigley, HA, Hohman, RM. (1983). Laser energy levels for trabecular meshwork damage in the primate eye. Invest Ophthalmol Vis Sci. 24. 1305-1317
- Weber, AJ, Zelenak, D. (2001). Experimental glaucoma in the primate induced by latex microspheres. J Neurosci Methods. 111. 39-48
- Morrison, JC, Moore, CG, Deppmeier, LM, Gold, BG, Meshul, CK, Johnson, EC. (1997). A rat model of chronic pressure-induced optic nerve damage. Exp Eye Res. 64. 85-96
- Shareef, SR, Garcia-Valenzuela, E, Salierno, A, Walsh, J, Sharma, SC. (1995). Chronic ocular hypertension following episcleral venous occlusion in rats. Exp Eye Res. 61. 379-382
- Ruiz-Ederra, J, Garcia, M, Hernandez, M, Urcola, H, Hernandez-Barbachano, E, Araiz, J. (2005). The pig eye as a novel model of glaucoma. Exp Eye Res.
- Garway-Heath, DF, Holder, GE, Fitzke, FW, Hitchings, RA. (2002). Relationship between electrophysiological, psychophysical, and anatomical measurements in glaucoma. Invest Ophthalmol Vis Sci. 43. 2213-2220
- Ahmed, FA, Chaudhary, P, Sharma, SC. (2001). Effects of increased intraocular pressure on rat retinal ganglion cells. Int J Dev Neurosci. 19. 209-218
- Kirby, MA, Chalupa, LM. (1986). Retinal crowding alters the morphology of alpha ganglion cells. J Comp Neurol. 251. 532-541
- Perry, VH, Linden, R. (1982). Evidence for dendritic competition in the developing retina. Nature. 297. 683-685
- Morgan, JE, Uchida, H, Caprioli, J. (2000). Retinal ganglion cell death in experimental glaucoma. Br J Ophthalmol. 84. 303-310