Mechanisms of iron porphyrin reactions with peroxynitrite

被引:154
作者
Lee, JB [1 ]
Hunt, JA [1 ]
Groves, JT [1 ]
机构
[1] Princeton Univ, Dept Chem, Princeton, NJ 08544 USA
关键词
D O I
10.1021/ja980507y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Peroxynitrite (ONOO-)is a major cytotoxic agent that has been implicated in a host of pathophysiological conditions; it is therefore important to develop therapeutic agents to detoxify this potent biological oxidant, and to understand the modes of action of these agents. Water-soluble iron porphyrins, such as 5,10,15,20-tetrakis(N-methyl-4'-pyridyl)porphinatoiron(III) [Fe(III)TMPyP] and 5,10,15,20-tetrakis-(2,4,6-trimethyl-3,5-sulfonatophenyl)porphinatoiron(III) [Fe(III)TMPS], have been shown to catalyze the efficient decomposition of ONOO- to NO3- and NO2- under physiological conditions. However, the mechanisms of ONOO- decomposition catalyzed by these water-soluble iron porphyrins have not yet been elucidated. We have shown that there are two different pathways operating in the catalytic decomposition of ONOO- by FeTMPyP. Fe(III)TMPyP reacts rapidly with ONOO- to produce oxoFe(IV)TMPyP and NO2 (k approximate to 5 x 10(7) M-1 s(-1)). The oxoFe(IV) porphyrin, which persisted throughout the catalytic decomposition of ONOO-, was shown to be relatively unreactive toward NO2- and NO2-. This oxoFe(IV) porphyrin was also shown to react with ONOO- (k = 1.8 x 10(6) M-1 s(-1)), and it was this oxoFe(TV)-ONOO- reaction pathway that predominated under conditions of excess ONOO- with respect to Fe(III)TMPyP. The competition between the two pathways explains the highly nonlinear relationship observed for k(cat) with respect to ONOO- concentration. Fe(III)-TMPyP is also known to catalyze the dismutation of the ONOO- precursor superoxide (O2(-.)), and using stopped-flow spectrophotometry, the rate of Fe(III)TMPyP-catalyzed O-2(-.) dismutation has been determined to be 1.9 x 10(7) M-1 s(-1) by direct measurement. A detailed mechanistic understanding of how iron porphyrins function in the catalytic decomposition of both ONOO- and O-2(-.) may prove essential in the exploration of the chemistry and biology of these reactive oxygen species, and in understanding the biological activity of these metalloporphyrins.
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页码:7493 / 7501
页数:9
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