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Citation
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HERO ID
1049069
Reference Type
Journal Article
Title
A mechanistic study of the photooxidation of A2E, a component of human retinal lipofuscin
Author(s)
Gaillard, ER; Avalle, LB; Keller, LM; Wang, Z; Reszka, KJ; Dillon, JP
Year
2004
Is Peer Reviewed?
Yes
Journal
Experimental Eye Research
ISSN:
0014-4835
EISSN:
1096-0007
Volume
79
Issue
3
Page Numbers
313-319
Language
English
PMID
15336493
DOI
10.1016/j.exer.2004.05.005
Web of Science Id
WOS:000223973400003
Abstract
A major constituent of human retinal lipofuscin is A2E (2-[2,6-dimethyl-8-(2,6,6-trimethyl-1-cyclohexen-1-yl)-1E,3E,5E,7E-octatetraenyl]-1-(2-hydroxyethyl)-4-[4-methyl-6(2,6,6-trimethyl-1-cyclohexen-1-yl)-1E,3E,5E,7E-hexatrienyl]-pyridinium). Light transmitted by the lens is absorbed by A2E and the processes initiated by this absorption has been implicated in several maculopothies. The purpose of this study was to evaluate the dominant photochemical mechanisms involved in these reactions, whether through free radical or singlet oxygen intermediacy. The photodestruction of A2E occurs faster in water vs. chloroform and hydrogenated vs. perdeuterated methanol. Both results suggest a free radical mechanism. Product distributions indicate sequential oxygen addition rather than the addition of two oxygen atoms which would be expected if singlet oxygen was an intermediate. Finally, EPR trapping studies lead to the detection of superoxide as the primary intermediate in the photochemical reactions. It is concluded that if singlet oxygen is involved in these photochemical processes it is of minor importance.
Keywords
A2E; lipofuscin; RPE; photooxidation; AMD; free radicals; superoxide
Tags
•
Chloroform Combined (current)
Chloroform (original)
References: 2000-2018
WoS
•
Methanol (Non-Cancer)
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WOS
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