Youssefi A A, Arutyunyan R, Emerit I
Department of Genetics, Centre de Recherches Biomédicales des Cordeliers, CNRS, Paris, France.
Mutat Res. 1994 Sep 1;309(2):185-91. doi: 10.1016/0027-5107(94)90091-4.
Besides the direct interaction of psoralens with DNA and other macromolecules, the role of reactive oxygen species in the PUVA-induced cellular injury has been stressed. The present study shows that treatment of human blood cultures with 5-methoxypsoralen or 8-methoxypsoralen, followed by UVA exposure, results in chromosome damage. The supernatant of these cultures contains secondarily formed chromosome damaging material, called clastogenic factor (CFs). Not only CF formation, but also CF action is inhibited by superoxide dismutase (SOD), suggesting that superoxide is formed on the pathway to chromosome aberration. CF is detectable in the cell culture supernatants after a minimal delay of 18 h, and reaches a plateau at 24 h of cultivation. SOD is no longer protective if added after 24 h, i.e., the enzyme can prevent, but not repair the oxyradical-induced damage.
除了补骨脂素与DNA及其他大分子的直接相互作用外,活性氧物质在光化学疗法(PUVA)诱导的细胞损伤中的作用也受到了关注。本研究表明,用5-甲氧基补骨脂素或8-甲氧基补骨脂素处理人体血液培养物,随后进行长波紫外线(UVA)照射,会导致染色体损伤。这些培养物的上清液含有次生形成的染色体损伤物质,称为致裂因子(CFs)。超氧化物歧化酶(SOD)不仅抑制CF的形成,还抑制CF的作用,这表明超氧化物是在导致染色体畸变的途径中形成的。在培养18小时的最短延迟后,可在细胞培养上清液中检测到CF,并在培养24小时时达到平台期。如果在24小时后添加SOD,则不再具有保护作用,即该酶可以预防但不能修复氧自由基诱导的损伤。