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Time‐resolved and Steady‐state Fluorescence Spectroscopic Studies of the Human Lens with Comparison to Argpyrimidine, Pentosidine and 3‐OH‐kynurenine ¶
Author(s) -
Kessel Line,
Kalinin Stanislav,
Nagaraj Ram H.,
Larsen Michael,
Johansson Lennart B.Å.
Publication year - 2002
Publication title -
photochemistry and photobiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.818
H-Index - 131
eISSN - 1751-1097
pISSN - 0031-8655
DOI - 10.1562/0031-8655(2002)0760549trassf2.0.co2
Subject(s) - pentosidine , autofluorescence , fluorescence , kynurenine , tryptophan , chemistry , glycation , lens (geology) , biophysics , photochemistry , biochemistry , optics , biology , amino acid , physics , receptor
The intrinsic fluorescence from the human lens on excitation in the UV region, referred to as blue lens autofluorescence, increases with age or in the presence of diabetes. The present study reveals that the relative contribution of compounds responsible for the blue autofluorescence appears to be a constant with age. Three potential candidates for the blue fluorescence were also studied with respect to fluorescence spectroscopic properties. These were argpyrimidine and pentosidine, both advanced glycation end products, and 3‐hydroxykynurenine (3‐OH‐kynurenine), a photooxidative derivative of tryptophan. It was shown that the spectral properties of argpyrimidine and pentosidine are compatible with the observed blue fluorescence of the human lens, whereas the fluorescence from 3‐OH‐kynurenine is negligible.