The photochemical behavior of 5-S-cysteinyldopa (5-S-CD), a colorless product of melanocyte metabolism, was investigated in neutral phosphate buffer with biologically relevant UV radiation. Exposure of 5-S-CD to pyrex-filtered UV light (wavelengths > 320 nm) was found to induce an oxygen-dependent reaction, leading to, besides abundant polymeric materials, the benzothiazine derivatives I and II (two diastereoisomers). Superoxide dismutase exerted a small inhibitory effect on 5-S-CD consumption, whereas other active oxygen scavengers had no effect on. the reaction course. Addition of glutathione as a hydrogen donor completely suppressed the reaction. With UVB light (wavelength range 280-320 nm) photolysis of 5-S-CD proceeded mainly with formation of 3,4-dihydroxy-phenylalanine, arising presumably by photohomolytic cleavage of the S-CH2 bond followed by desulfuration. These results are of interest in relation to the high susceptibility of fair-complexioned individuals to actinic damage and skin cancer.
Photochemistry of 5-S-cysteinyldopa / D'Ischia, Marco; C., Costantini; G., Prota; A. P. A. L. U. M. B., O.. - In: PHOTOCHEMISTRY AND PHOTOBIOLOGY. - ISSN 0031-8655. - STAMPA. - 60:(1994), pp. 33-37.
Photochemistry of 5-S-cysteinyldopa
D'ISCHIA, MARCO;
1994
Abstract
The photochemical behavior of 5-S-cysteinyldopa (5-S-CD), a colorless product of melanocyte metabolism, was investigated in neutral phosphate buffer with biologically relevant UV radiation. Exposure of 5-S-CD to pyrex-filtered UV light (wavelengths > 320 nm) was found to induce an oxygen-dependent reaction, leading to, besides abundant polymeric materials, the benzothiazine derivatives I and II (two diastereoisomers). Superoxide dismutase exerted a small inhibitory effect on 5-S-CD consumption, whereas other active oxygen scavengers had no effect on. the reaction course. Addition of glutathione as a hydrogen donor completely suppressed the reaction. With UVB light (wavelength range 280-320 nm) photolysis of 5-S-CD proceeded mainly with formation of 3,4-dihydroxy-phenylalanine, arising presumably by photohomolytic cleavage of the S-CH2 bond followed by desulfuration. These results are of interest in relation to the high susceptibility of fair-complexioned individuals to actinic damage and skin cancer.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
