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The effect of L‐cysteine and N‐acetylcysteine on porphyrin/heme biosynthetic pathway in cells treated with 5‐aminolevulinic acid and exposed to radiation
Author(s) -
He D.,
Behar S.,
Roberts J. E.,
Lim H. W.
Publication year - 1996
Publication title -
photodermatology, photoimmunology and photomedicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.736
H-Index - 60
eISSN - 1600-0781
pISSN - 0905-4383
DOI - 10.1111/j.1600-0781.1996.tb00199.x
Subject(s) - a431 cells , ferrochelatase , epidermoid carcinoma , cell culture , acetylcysteine , heme , porphyrin , microbiology and biotechnology , chemistry , cysteine , photosensitizer , biochemistry , cell , biology , cell cycle , enzyme , carcinoma , photochemistry , genetics , molecular medicine , antioxidant
The effects of L‐cysteine (LC) and N‐acetylcysteine (NAC) on porphyrin accumulation in a human dermal microvascular endothelial cell line (HMEC‐1) and a human epidermoid carcinoma cell line (A431) loaded with 5‐aminolevulinic acid (ALA) and exposed to ultraviolet A (UVA) and blue light radiation were determined. Porphyrin accumulation was decreased in the presence of 0.1–7.5 mM LC (24.8%‐31.4% suppression in HMEC‐1 cell; 35.8%‐48.9% suppression in A431 cells), and in the presence of 0.1–10.0 mM NAC (30.9%‐58.0% suppression in HMEC‐1 cells; 8.5%‐45.3% in A431 cells). The suppression occurred in a LC or NAC dose‐dependent fashion. The above was associated with partial reversal of suppression of ferrochelatase (FeC) activity in HMEC‐1 cells and in A431 cells. As compared to FeC activity in cells treated with ALA and irradiation, enzyme activity was higher (by 31.9%‐62.1%) in the presence of LC (1.0 mM or 5.0 mM) and in the presence of NAC (1.0 mM or 5.0 mM). These data indicate that LC and NAC have protective effects on porphyrin‐ and irradiation‐induced diminution of FeC activity in HMEC‐1 cells and A431 cells in vitro.