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Stability and reaction of the dithiocarbamate-ferrous-NO complex in PMA-stimulated peritoneal macrophages

机译:二硫代氨基甲酸酯-亚铁-NO配合物在PMA刺激的腹膜巨噬细胞中的稳定性和反应

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摘要

In this study the stability of the NO spin-trapping complex, (dithiocarbamate)_2Fe~(2+) NO and its interaction with rat peritoneal macrophages was investigated. The stability experiments showed that DTCS (dithiocarboxy sarcosine) trapping complex was more stable than that of MGD (N-methyl-D-glucamine-dithiocarbamate) in macrophages activated by PMA (phorbol-1,2-myristate-1,3-acetate) and L-arginine. Free radical species, O_2~(·-) and NO, generated in macrophages respiratory burst were causative for the instability of the NO trapping complex. Addition of more dithiocarbamate and ferrous salt could increase the stability of the trapping complex in the system. Dithiocarbamate and ferrous salt did not impair the oxygen consumption of macrophages. The increasing effects of dithiocarbamate derivatives and ferrous salt on the stability of the trapping complex may be due to their scavenging effects on the free radicals generated by macrophages and their ability to inhibit the oxidation of ferrous ion in the (dithiocarbamate)_2Fe~(2+)NO complex.
机译:本研究研究了自旋捕获复合物(二硫代氨基甲酸酯)_2Fe〜(2+)NO的稳定性及其与大鼠腹膜巨噬细胞的相互作用。稳定性实验表明,在被PMA激活的巨噬细胞中,DTCS(二硫代羧基肌氨酸)捕获复合物比MGD(N-甲基-D-葡糖胺-二硫代氨基甲酸酯)捕获复合物更稳定(佛波醇1,2-肉豆蔻酸酯-1,3-乙酸酯)。和L-精氨酸。巨噬细胞呼吸爆发中产生的自由基O_2〜(·-)和NO是造成NO捕集络合物不稳定的原因。添加更多的二硫代氨基甲酸酯和亚铁盐可以提高系统中捕集配合物的稳定性。二硫代氨基甲酸酯和亚铁盐不会损害巨噬细胞的耗氧量。二硫代氨基甲酸酯衍生物和亚铁盐对捕集配合物稳定性的增加作用可能是由于它们对巨噬细胞产生的自由基的清除作用以及它们抑制(二硫代氨基甲酸酯)_2Fe〜(2+没有复杂的

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