Samocha-Bonet Dorit, Lichtenberg Dov, Pinchuk Ilya
Department of Physiology and Pharmacology, Sackler Medical School, Tel Aviv University, 69978 Tel Aviv, Israel.
J Inorg Biochem. 2005 Oct;99(10):1963-72. doi: 10.1016/j.jinorgbio.2005.06.006.
Urate and ascorbate are the major water-soluble low molecular weight antioxidants in serum. Much attention has been devoted to the effect of these antioxidants on lipoprotein peroxidation in vivo and on their effect on copper-induced peroxidation ex vivo. These studies revealed that urate inhibits ascorbate oxidation in vitro, whereas the effect of ascorbate on urate oxidation has not been systematically studied thus far. The present study addresses mechanistic aspects of the kinetics of copper-induced oxidation of both these antioxidants and their mutual effects in aqueous solutions. We found that: (i) ascorbate becomes oxidized much faster than urate. (ii) Urate inhibits the oxidation of ascorbate but, even in the presence of excess urate, ascorbate becomes oxidized much faster than urate. (iii) Ascorbate, as well as the products of its oxidation (and/or hydrolysis) inhibit the copper-induced oxidation of urate. All these results are consistent with the hypothesis that the rate of ascorbate oxidation is determined by the rate of reoxidation of reduced copper (Cu(I)) to Cu(II) by molecular oxygen, whereas the rate of urate oxidation is governed by the rate of oxidation of urate within a 2:1 urate/copper complex. We think that the mutual effects of urate and ascorbate on each other's oxidation are likely to enhance their inhibitory effect on lipid peroxidation in biologically relevant systems including membranes and lipoproteins.
尿酸盐和抗坏血酸盐是血清中主要的水溶性低分子量抗氧化剂。这些抗氧化剂对体内脂蛋白过氧化的影响以及它们对体外铜诱导的过氧化的影响已受到广泛关注。这些研究表明,尿酸盐在体外抑制抗坏血酸盐的氧化,而迄今为止,抗坏血酸盐对尿酸盐氧化的影响尚未得到系统研究。本研究探讨了铜诱导的这两种抗氧化剂氧化动力学的机制方面以及它们在水溶液中的相互作用。我们发现:(i)抗坏血酸盐比尿酸盐氧化得快得多。(ii)尿酸盐抑制抗坏血酸盐的氧化,但即使存在过量的尿酸盐,抗坏血酸盐的氧化速度也比尿酸盐快得多。(iii)抗坏血酸盐及其氧化(和/或水解)产物抑制铜诱导的尿酸盐氧化。所有这些结果都与以下假设一致,即抗坏血酸盐的氧化速率由分子氧将还原态铜(Cu(I))再氧化为Cu(II)的速率决定,而尿酸盐的氧化速率由尿酸盐在2:1尿酸盐/铜络合物中的氧化速率控制。我们认为,尿酸盐和抗坏血酸盐对彼此氧化的相互作用可能会增强它们在包括膜和脂蛋白在内的生物相关系统中对脂质过氧化的抑制作用。