Oxidative damage and age-related macular degeneration.

B. S. Winkler, M. E. Boulton, J. D. Gottsch, P. Sternberg

Research output: Contribution to journalArticle

550 Citations (Scopus)

Abstract

This article provides current information on the potential role of oxidation in relation to age-related macular degeneration (AMD). The emphasis is placed on the generation of oxidants and free radicals and the protective effects of antioxidants in the outer retina, with specific emphasis on the photoreceptor cells, the retinal pigment epithelium and the choriocapillaris. The starting points include a discussion and a definition of what radicals are, their endogenous sources, how they react, and what damage they may cause. The photoreceptor/pigment epithelium complex is exposed to sunlight, is bathed in a near-arterial level of oxygen, and membranes in this complex contain high concentrations of polyunsaturated fatty acids, all considered to be potential factors leading to oxidative damage. Actions of antioxidants such as glutathione, vitamin C, superoxide dismutase, catalase, vitamin E and the carotenoids are discussed in terms of their mechanisms of preventing oxidative damage. The phototoxicity of lipofuscin, a group of complex autofluorescent lipid/protein aggregates that accumulate in the retinal pigment epithelium, is described and evidence is presented suggesting that intracellular lipofuscin is toxic to these cells, thus supporting a role for lipofuscin in aging and AMD. The theory that AMD is primarily due to a photosensitizing injury to the choriocapillaris is evaluated. Results are presented showing that when protoporphyric mice are exposed to blue light there is an induction in the synthesis of Type IV collagen synthesis by the choriocapillary endothelium, which leads to a thickened Bruch's membrane and to the appearance of sub-retinal pigment epithelial fibrillogranular deposits, which are similar to basal laminar deposits. The hypothesis that AMD may result from oxidative injury to the retinal pigment epithelium is further evaluated in experiments designed to test the protective effects of glutathione in preventing damage to cultured human pigment epithelial cells exposed to an oxidant. Experiments designed to increase the concentration of glutathione in pigment epithelial cells using dimethylfumarate, a monofunctional inducer, are described in relation to the ability of these cells to survive an oxidative challenge. While all these models provide undisputed evidence of oxidative damage to the retinal pigment epithelium and the choriocapillaris that is both light- and oxygen-dependent, it nevertheless is still unclear at this time what the precise linkage is between oxidation-induced events and the onset and progression of AMD.

Original languageEnglish (US)
Pages (from-to)32
Number of pages1
JournalMolecular Vision
Volume5
StatePublished - Nov 3 1999
Externally publishedYes

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Macular Degeneration
Retinal Pigment Epithelium
Lipofuscin
Glutathione
Oxidants
Antioxidants
Epithelial Cells
Bruch Membrane
Oxygen
Phototoxic Dermatitis
Light
Photoreceptor Cells
Retinal Pigments
Collagen Type IV
Sunlight
Poisons
Wounds and Injuries
Carotenoids
Unsaturated Fatty Acids
Vitamin E

ASJC Scopus subject areas

  • Ophthalmology

Cite this

Winkler, B. S., Boulton, M. E., Gottsch, J. D., & Sternberg, P. (1999). Oxidative damage and age-related macular degeneration. Molecular Vision, 5, 32.

Oxidative damage and age-related macular degeneration. / Winkler, B. S.; Boulton, M. E.; Gottsch, J. D.; Sternberg, P.

In: Molecular Vision, Vol. 5, 03.11.1999, p. 32.

Research output: Contribution to journalArticle

Winkler, BS, Boulton, ME, Gottsch, JD & Sternberg, P 1999, 'Oxidative damage and age-related macular degeneration.', Molecular Vision, vol. 5, pp. 32.
Winkler BS, Boulton ME, Gottsch JD, Sternberg P. Oxidative damage and age-related macular degeneration. Molecular Vision. 1999 Nov 3;5:32.
Winkler, B. S. ; Boulton, M. E. ; Gottsch, J. D. ; Sternberg, P. / Oxidative damage and age-related macular degeneration. In: Molecular Vision. 1999 ; Vol. 5. pp. 32.
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