Winterbourn C C
Pathology Department, Christchurch School of Medicine, Christchurch Hospital, New Zealand.
Arch Biochem Biophys. 1989 Jun;271(2):447-55. doi: 10.1016/0003-9861(89)90295-6.
The effects of GSH on the autoxidation of the fava bean pyrimidine aglycones, divicine and isouramil, and on acid-hydrolyzed vicine (provisional identification 2-amino-4,5,6-trihydroxypyrimidine) have been studied. GSH alone promoted redox cycling of each compound, with concomitant GSH oxidation and H2O2 production. In the presence of superoxide dismutase, there is a lag period during which little pyrimidine oxidation occurs, followed by a period of accelerated oxidation. With the three pyrimidines, increasing concentrations of GSH extended this lag period and progressively decreased subsequent rates of both pyrimidine oxidation and O2 uptake. No GSH oxidation or O2 uptake occurred during the lag. These results show that the combination of GSH and superoxide dismutase is able to inhibit redox cycling of the pyrimidines. With a 10-fold excess of GSH over isouramil or acid-hydrolyzed vicine (20-fold with divicine) this coupled oxidation of GSH and the pyrimidine is almost completely suppressed. This mechanism may be a means whereby GSH in combination with superoxide dismutase protects against the cytotoxic effects of these reactive pyrimidines.
已研究了谷胱甘肽(GSH)对蚕豆嘧啶苷元(divicine和异脲嘧啶)以及酸水解后的巢菜碱(暂定鉴定为2-氨基-4,5,6-三羟基嘧啶)自氧化的影响。单独的GSH促进了每种化合物的氧化还原循环,同时伴有GSH氧化和过氧化氢生成。在超氧化物歧化酶存在的情况下,存在一个延迟期,在此期间嘧啶氧化很少发生,随后是加速氧化期。对于这三种嘧啶,GSH浓度的增加延长了该延迟期,并逐渐降低了随后嘧啶氧化和氧气摄取的速率。在延迟期内未发生GSH氧化或氧气摄取。这些结果表明,GSH和超氧化物歧化酶的组合能够抑制嘧啶的氧化还原循环。当GSH比异脲嘧啶或酸水解后的巢菜碱过量10倍(比divicine过量20倍)时,GSH与嘧啶的这种偶联氧化几乎被完全抑制。这种机制可能是GSH与超氧化物歧化酶结合起来防止这些活性嘧啶产生细胞毒性作用的一种方式。