Palumbo A, Astarita G, d'Ischia M
Zoological Station 'Anton Dohrn', Villa Comunale, I-80121 Naples, Italy.
Biochem J. 2001 May 15;356(Pt 1):105-10. doi: 10.1042/0264-6021:3560105.
6-Nitrodopamine and 6-nitronoradrenaline (6-nitronorepinephrine), putative products of the nitric oxide (NO)-dependent nitration of dopamine and noradrenaline, are reported to be reversible, competitive inhibitors of neuronal nitric oxide synthase (nNOS) with K(i) values of 45 and 52 microM respectively. The nitrocatecholamines inhibited H(2)O(2) production in the absence of L-arginine and tetrahydrobiopterin (BH(4)) (the IC(50) values for 6-nitrodopamine and 6-nitronoradrenaline were 85 and 55 microM respectively) but without affecting cytochrome c reduction. The apparent K(i) values for nitrocatecholamine inhibition of enzyme activation by BH(4) were 18 microM for 6-nitrodopamine and 40 microM for 6-nitronoradrenaline. Both nitrocatecholamines antagonized the dimerization of nNOS induced by BH(4) and by L-arginine, the effect being reversed by BH(4) (more than 10 microM) and L-arginine (e.g. 100 microM). Overall, these results suggest that nitrocatecholamines interfere with nNOS activity by binding to the enzyme in the proximity of the substrate and BH(4)-binding sites near the haem group.
6-硝基多巴胺和6-硝基去甲肾上腺素(6-硝基去甲肾上腺素)是多巴胺和去甲肾上腺素依赖一氧化氮(NO)硝化作用的推定产物,据报道它们是神经元型一氧化氮合酶(nNOS)的可逆竞争性抑制剂,其抑制常数(K(i))值分别为45和52微摩尔。在没有L-精氨酸和四氢生物蝶呤(BH(4))的情况下,硝基儿茶酚胺抑制过氧化氢(H(2)O(2))的产生(6-硝基多巴胺和6-硝基去甲肾上腺素的半数抑制浓度(IC(50))值分别为85和55微摩尔),但不影响细胞色素c的还原。6-硝基多巴胺对BH(4)激活酶的抑制作用的表观K(i)值为18微摩尔,6-硝基去甲肾上腺素为40微摩尔。两种硝基儿茶酚胺均拮抗由BH(4)和L-精氨酸诱导的nNOS二聚化,这种作用可被BH(4)(超过10微摩尔)和L-精氨酸(例如100微摩尔)逆转。总体而言,这些结果表明硝基儿茶酚胺通过在底物和血红素基团附近的BH(4)结合位点附近与酶结合来干扰nNOS活性。