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Determination of S ‐[2‐carboxy‐1‐(1 H ‐imidazol‐ 4‐yl)ethyl]glutathione, a novel metabolite of L ‐histidine, in tissue extracts from sunlight‐ irradiated rat by capillary electrophoresis
Author(s) -
Kinuta Masahiro,
Ohta Jun,
Yamada Hiroshi,
Kinuta Keiko,
Abe Tadashi,
Li ShunAi,
Otsuka Atsushi,
Nakanishi Akira,
Takei Kohji
Publication year - 2001
Publication title -
electrophoresis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.666
H-Index - 158
eISSN - 1522-2683
pISSN - 0173-0835
DOI - 10.1002/1522-2683(200109)22:16<3365::aid-elps3365>3.0.co;2-m
Subject(s) - urocanic acid , metabolite , chemistry , glutathione , histidine , adduct , biochemistry , capillary electrophoresis , metabolism , kidney , chromatography , amino acid , enzyme , biology , organic chemistry , endocrinology
Abstract Exposure of the skin to sunlight results in an increase in the content of epidermal urocanic acid, a key metabolite of L ‐histidine, and some portions of the metabolite penetrate into the body fluid. S ‐[2‐Carboxy‐1‐(1 H ‐imidazol‐4‐yl)ethyl]glutathione (GS(CIE)), an adduct of glutathione and urocanic acid, was proposed to be an origin of a urinary compound, S ‐[2‐carboxy‐1‐(1 H ‐imidazol‐4‐yl)ethyl]‐ L ‐cysteine (Cys(CIE)). Various catabolites of Cys(CIE) were also isolated from human urine previously. However, no direct evidence to show the existence of GS(CIE) as a biological material had been found. By using capillary electrophoresis, the glutathione adduct has now been found in the extracts of rat tissues from the kidney, liver, skin and blood when the rat was kept under conditions of sunlight irradiation after the fur on the dorsal skin had been clipped. On the other hand, no or a trace of GS(CIE) was determined in rat tissue extracts when the animal was kept indoor in usual manner. The glutathione adduct was isolated from the kidney extract of the sunlight‐irradiated rat using ion‐exchangers and high‐voltage paper electrophoresis, and determined by fast‐atom‐bombardment mass spectrometry. These results indicate that GS(CIE) formation actually occurs in the body and that the formation is accelerated by exposing the rat to sunlight irradiation. From these findings, we propose an alternative pathway of histidine metabolism which is initiated by the adduction of urocanic acid to glutathione to form GS(CIE) and terminates with the formation of the urinary compounds via Cys(CIE).