There is growing awareness that lutein and zeaxanthin may be important protective factors against visual loss from age-related macular degeneration (AMD), the leading cause of irreversible blindness in the developed world. These xanthophyll carotenoids are derived exclusively from the diet, and they are concentrated at very high levels in the human macula with extraordinarily high specificity. They are thought to protect against age-related damage to the macula through anti-oxidant and light-screening mechanisms. Whenever a tissue exhibits selective uptake of a compound, the process is likely to be mediated through specific binding proteins, and detailed analysis of carotenoid oxidation products in the eye suggests that the retina is a site for active metabolic interconversions of dietary lutein and zeaxanthin and their metabolites. The enzymes and binding proteins involved in these pathways will be characterized and isolated from human donor eyes. Particular emphasis will be placed on the pi isoform of glutathione S-transferase (GSTP1), an enzyme recently identified in this laboratory as likely to be involved in the conversion of lutein to zeaxanthin in the human eye. Defects in carotenoid binding and metabolic pathways could have severe consequences on normal macular function. Stable isotope methods will be used to study the phamacokinetics of carotenoid uptake, clearance, and metabolism in the eyes of small animal models. These studies may lead to improved and more rational strategies for raising macular carotenoid levels in individuals at risk for visual loss from AMD. Resonance Raman spectroscopy has proven to be a powerful objective method for the noninvasive assessment of macular carotenoid levels. An imaging mode of this technique will be used to map the distribution of carotenoids in human donor eyes and in the primate retina with previously unobtainable resolution and specificity. This information will provide valuable insights into the physiology of the macular pigments in the normal eye and a greater understanding of the alterations that may occur in association with aging and degenerative processes.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY011600-08
Application #
7059920
Study Section
Biology and Diseases of the Posterior Eye Study Section (BDPE)
Program Officer
Mariani, Andrew P
Project Start
1997-08-01
Project End
2007-04-30
Budget Start
2006-05-01
Budget End
2007-04-30
Support Year
8
Fiscal Year
2006
Total Cost
$291,974
Indirect Cost
Name
University of Utah
Department
Ophthalmology
Type
Schools of Medicine
DUNS #
009095365
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
Andersen, Karl M; Sauer, Lydia; Gensure, Rebekah H et al. (2018) Characterization of Retinitis Pigmentosa Using Fluorescence Lifetime Imaging Ophthalmoscopy (FLIO). Transl Vis Sci Technol 7:20
Arunkumar, Ranganathan; Calvo, Charles M; Conrady, Christopher D et al. (2018) What do we know about the macular pigment in AMD: the past, the present, and the future. Eye (Lond) 32:992-1004
Sauer, Lydia; Gensure, Rebekah H; Hammer, Martin et al. (2018) Fluorescence Lifetime Imaging Ophthalmoscopy: A Novel Way to Assess Macular Telangiectasia Type 2. Ophthalmol Retina 2:587-598
Conrady, Christopher D; Bell, James P; Besch, Brian M et al. (2017) Correlations Between Macular, Skin, and Serum Carotenoids. Invest Ophthalmol Vis Sci 58:3616-3627
Hatori, Megumi; Gronfier, Claude; Van Gelder, Russell N et al. (2017) Global rise of potential health hazards caused by blue light-induced circadian disruption in modern aging societies. NPJ Aging Mech Dis 3:9
Gorusupudi, Aruna; Nelson, Kelly; Bernstein, Paul S (2017) The Age-Related Eye Disease 2 Study: Micronutrients in the Treatment of Macular Degeneration. Adv Nutr 8:40-53
Li, Binxing; Vachali, Preejith P; Shen, Zhengqing et al. (2017) Retinal accumulation of zeaxanthin, lutein, and ?-carotene in mice deficient in carotenoid cleavage enzymes. Exp Eye Res 159:123-131
Choi, Rene Y; Gorusupudi, Aruna; Wegner, Kimberley et al. (2017) MACULAR PIGMENT DISTRIBUTION RESPONSES TO HIGH-DOSE ZEAXANTHIN SUPPLEMENTATION IN PATIENTS WITH MACULAR TELANGIECTASIA TYPE 2. Retina 37:2238-2247
Shyam, Rajalekshmy; Vachali, Preejith; Gorusupudi, Aruna et al. (2017) All three human scavenger receptor class B proteins can bind and transport all three macular xanthophyll carotenoids. Arch Biochem Biophys 634:21-28
Shyam, Rajalekshmy; Gorusupudi, Aruna; Nelson, Kelly et al. (2017) RPE65 has an additional function as the lutein to meso-zeaxanthin isomerase in the vertebrate eye. Proc Natl Acad Sci U S A 114:10882-10887

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