Alterations of aqueous humour outflow following argon laser trabeculoplasty in monkeys.

We performed argon laser trabeculoplasty in one eye in each of three cynomolgus monkeys, leaving the contralateral eyes as controls. Four weeks later in both eyes of each monkey we infused cationized ferritin as a tracer of the aqueous outflow pathways for 30-40 minutes before fixation. In the control eyes cationized ferritin was found throughout the conventional aqueous outflow tract, labelling trabecular endothelial cells, both inner and outer walls of Schlemm's canal, and the collecting channels. No permeation of cationized ferritin through continuous cellular layers such as the corneal endothelium was detected. In the lasered spots of the treated eyes cationized ferritin was found to label the cellular sheet covering the trabecular scar at the lasered site, but no tracer was detected within the scar or in Schlemm's canal immediately beneath. In contrast in adjacent non-lasered regions the trabecular cells, the observed juxta-canalicular herniations, and the vacuoles of the inner wall as well as Schlemm's canal itself were extensively labelled. Our findings suggest impermeability to aqueous humour flow through the actual lasered lesion, with shift of flow to adjacent, non-lasered regions. In the normal monkey these regions compensate structurally and functionally in ways that may help to deal with this diverted flow.

[1]  D. Epstein,et al.  Delayed response to argon laser trabeculoplasty in monkeys. Morphological and morphometric analysis. , 1986, Archives of ophthalmology.

[2]  D. Epstein,et al.  Use of cationized ferritin to trace aqueous humor outflow in the monkey eye. , 1986, Experimental eye research.

[3]  D. Epstein,et al.  Short-term effect of argon laser trabeculoplasty in monkeys. , 1985, Archives of ophthalmology.

[4]  J. M. Butler,et al.  Asymmetric distribution of charged domains on the two fronts of the endothelium of iris blood vessels. , 1985, Investigative ophthalmology & visual science.

[5]  M. Koss,et al.  Acute intraocular pressure elevation produced by argon laser trabeculoplasty in the cynomolgus monkey. , 1984, Archives of ophthalmology.

[6]  D. Samuelson,et al.  Kinetics of phagocytosis in the normal canine iridocorneal angle. , 1984, American journal of veterinary research.

[7]  G. Spaeth,et al.  Histopathologic verification of position of laser burns in argon laser trabeculoplasty. , 1984, Ophthalmic surgery.

[8]  E. V. Van Buskirk,et al.  Argon laser trabeculoplasty. Studies of mechanism of action. , 1984 .

[9]  L. Hazlett,et al.  Complex carbohydrates at the ocular surface of the mouse: an ultrastructural and cytochemical analysis. , 1984, Experimental eye research.

[10]  J. Alvarado,et al.  Trabecular meshwork cellularity in primary open-angle glaucoma and nonglaucomatous normals. , 1984, Ophthalmology.

[11]  B. Rao Argon laser therapy in open angle glaucoma. , 1983, Indian journal of ophthalmology.

[12]  H. Quigley,et al.  Laser energy levels for trabecular meshwork damage in the primate eye. , 1983, Investigative ophthalmology & visual science.

[13]  G. Spaeth,et al.  Electron microscopy of argon laser therapy in phakic open-angle glaucoma. , 1982, Ophthalmology.

[14]  T. Richardson Distribution of glycosaminoglycans in the aqueous outflow system of the cat. , 1982, Investigative ophthalmology & visual science.

[15]  J. Polansky,et al.  Age-related changes in trabecular meshwork cellularity. , 1981, Investigative ophthalmology & visual science.

[16]  J. B. Wise,et al.  Argon laser therapy for open-angle glaucoma. A pilot study. , 1979, Archives of ophthalmology.

[17]  W. R. Lee,et al.  THE APPEARANCE OF THE OUTFLOW APPARATUS OF THE EYE AFTER STAINING WITH RUTHENIUM RED , 1977, Acta ophthalmologica.

[18]  P. Kaufman,et al.  Light and electron microscopy of the anterior chamber angle structures following surgical disinsertion of the ciliary muscle in the cynomolgus monkey. , 1977, Investigative ophthalmology & visual science.

[19]  M. F. Armaly,et al.  Demonstration of acid mucopolysaccharides in the trabecular meshwork of the Rhesus monkey. , 1975, Investigative ophthalmology.

[20]  D. Gaasterland,et al.  Experimental glaucoma in the rhesus monkey. , 1974, Investigative ophthalmology.

[21]  R. Tripathi,et al.  The mechanism of aqueous outflow in birds. II. An ultrastructural study of perfused eyes. , 1973, Experimental eye research.

[22]  R. Tripathi,et al.  The mechanism of aqueous outflow in lower mammals. , 1972, Experimental eye research.

[23]  G. K. Smelser,et al.  Aqueous humor pathways through the trabecular meshwork and into Schlemm's canal in the cynomolgus monkey (Macaca irus). An electron microscopic study. , 1972, American journal of ophthalmology.

[24]  L. Goldstein,et al.  Use of cationized ferritin as a label of negative charges on cell surfaces. , 1972, Journal of ultrastructure research.

[25]  K. Segawa [Pores of the trabecular wall of Schlemm's canal. Ferritin perfusion in enucleated human eyes]. , 1970, Nippon Ganka Gakkai zasshi.

[26]  L. Feeney Outflow studies using an electron dense tracer. , 1966, Transactions - American Academy of Ophthalmology and Otolaryngology. American Academy of Ophthalmology and Otolaryngology.

[27]  L. Garron,et al.  Perfusion of human eyes with latex microspheres. , 1959, A.M.A. archives of ophthalmology.