Alegría Antonio E, Sanchez-Cruz Pedro, Rivas Lilyvet
Department of Chemistry, University of Puerto Rico at Humacao, CUH Station, Humacao, PR 00791.
Free Radic Biol Med. 2004 Nov 15;37(10):1631-9. doi: 10.1016/j.freeradbiomed.2004.07.030.
Ortho-quinones 1,10-phenanthroquinone and beta-lapachone but not para-quinones naphthazarin (NZQ) and 1,4-naphthoquinone enhance ascorbate oxidation in the presence of MgCl(2) and CaCl(2) at constant ionic strength. Alkaline-earth cation chelation is observed for the ortho-semiquinones but not for the para-semiquinones, while no interaction between these quinones (with the exception of NZQ) or ascorbate and these salts was detected, suggesting that semiquinone-metal complexes are responsible for the catalytic action on ascorbate oxidation of these metal salts in the presence of these ortho-quinones. Thus, redox cycling efficiency of the quinones under study here, in the presence of ascorbate, depends not only on the quinone redox potential but also on the semiquinone ability to chelate alkaline-earth cations.
邻醌类化合物1,10 - 菲醌和β - 拉帕醌,但对苯醌类化合物萘azarin(NZQ)和1,4 - 萘醌在MgCl₂和CaCl₂存在且离子强度恒定的情况下不会增强抗坏血酸的氧化。观察到邻半醌与碱土金属阳离子发生螯合作用,而对苯半醌则未观察到这种现象,同时未检测到这些醌类化合物(NZQ除外)或抗坏血酸与这些盐之间存在相互作用,这表明半醌 - 金属络合物是这些金属盐在这些邻醌存在下对抗坏血酸氧化起催化作用的原因。因此,在此研究的醌类化合物在抗坏血酸存在下的氧化还原循环效率不仅取决于醌的氧化还原电位,还取决于半醌螯合碱土金属阳离子的能力。