Pfeiffer S, Leopold E, Hemmens B, Schmidt K, Werner E R, Mayer B
Institut für Pharmakologie und Toxikologie, Karl-Franzens-Universität Graz, Austria.
Free Radic Biol Med. 1997;22(5):787-94. doi: 10.1016/s0891-5849(96)00407-8.
Carboxy-PTIO reacts rapidly with NO to yield NO2 and has been used as a scavenger to test the importance of nitric oxide (NO) in various physiological conditions. This study investigated the effects of carboxy-PTIO on several NO- and peroxynitrite-mediated reactions. The scavenger potently inhibited NO-induced accumulation of cGMP in endothelial cells but potentiated the effect of the putative peroxynitrite donor SIN-1, Carboxy-PTIO completely inhibited peroxynitrite-induced formation of 3-nitrotyrosine from free tyrosine (EC50 = 36 +/- 5 microM) as well as nitration of bovine serum albumin. Peroxynitrite-mediated nitrosation of GSH was stimulated by the drug with an EC50 of 0.12 +/- 0.03 mM, whereas S-nitrosation induced by the NO donor DEA/NO (0.1 mM) was inhibited by the scavenger with an IC50 of 0.11 +/- 0.03 mM. Oxidation of NO with carboxy-PTIO resulted in formation of nitrite without concomitant production of nitrate. Our results demonstrate that the effects of carboxy-PTIO are diverse and question its claimed specificity as NO scavenger.
羧基 - PTIO能迅速与一氧化氮(NO)反应生成二氧化氮(NO₂),并已被用作清除剂来检测一氧化氮在各种生理条件下的重要性。本研究调查了羧基 - PTIO对几种由NO和过氧亚硝酸盐介导的反应的影响。该清除剂能有效抑制NO诱导的内皮细胞中环鸟苷酸(cGMP)的积累,但增强了假定的过氧亚硝酸盐供体SIN - 1的作用。羧基 - PTIO完全抑制了过氧亚硝酸盐诱导的由游离酪氨酸形成3 - 硝基酪氨酸(半数有效浓度[EC50] = 36±5微摩尔/升)以及牛血清白蛋白的硝化作用。该药物刺激了过氧亚硝酸盐介导的谷胱甘肽(GSH)亚硝化反应,EC50为0.12±0.03毫摩尔/升,而由NO供体DEA/NO(0.1毫摩尔)诱导的S - 亚硝化反应则被该清除剂抑制,半数抑制浓度(IC50)为0.11±0.03毫摩尔/升。羧基 - PTIO与NO发生氧化反应生成亚硝酸盐,且没有伴随硝酸盐的产生。我们的结果表明,羧基 - PTIO的作用是多样的,并对其作为NO清除剂所宣称的特异性提出了质疑。