ZINC CONTENT OF HUMAN RETINAL-PIGMENT EPITHELIUM DECREASES WITH AGE AND MACULAR DEGENERATION, BUT SUPEROXIDE-DISMUTASE ACTIVITY INCREASES

Citation
Da. Newsome et al., ZINC CONTENT OF HUMAN RETINAL-PIGMENT EPITHELIUM DECREASES WITH AGE AND MACULAR DEGENERATION, BUT SUPEROXIDE-DISMUTASE ACTIVITY INCREASES, The Journal of trace elements in experimental medicine, 8(4), 1995, pp. 193-199
Citations number
17
Categorie Soggetti
Biology
ISSN journal
0896548X
Volume
8
Issue
4
Year of publication
1995
Pages
193 - 199
Database
ISI
SICI code
0896-548X(1995)8:4<193:ZCOHRE>2.0.ZU;2-7
Abstract
We previously reported an age-related decline of catalase activity and metallothionein (MT) in human retinal pigment epithelium (RPE) isolat ed from donor eyes. MT content and catalase activity also were shown t o decrease in RPE cells cultured in zinc-deficient medium. We now soug ht to determine whether zinc content and superoxide dismutase activity change with age and signs of macular degenerative disease in isolated human RPE. Eyes from 57 donors were graded with respect to disease by the presence or absence of visible drusen and macular pigment changes . RPE was collected from macular and peripheral regions. Tissues from 39 donors were separated into soluble and pigment granule fractions an d zinc content determined by flame atomic absorption spectroscopy. RPE from 18 separate donors was used for SOD activity analysis. Total RPE zinc was 9% lower in eyes from donors >70 years of age compared to th at from donors <age 70. Soluble macular zinc was 45% less in eyes >age 70 and showed a greater decline in the soluble fraction of macular RP E in eyes with signs of macular disease. Total SOD activity increased significantly (P < .05) with donor age. We conclude that zinc content decreased dramatically in the soluble fraction of macular RPE with age and signs of macular degeneration. Total SOD activity correlated nega tively with changes in zinc content. It remains to be determined wheth er the age-related decline in macular zinc is causal with respect to p reviously observed decreases in cellular MT and catalase. (C) 1996 Wil ey-Liss, Inc.