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2
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Tetrahydrobiopterin-dependent inhibition of superoxide generation from neuronal nitric oxide synthase.四氢生物蝶呤依赖性抑制神经元型一氧化氮合酶产生超氧阴离子。
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Identification of novel toxicity-associated metabolites by metabolomics and mass isotopomer analysis of acetaminophen metabolism in wild-type and Cyp2e1-null mice.通过代谢组学和对野生型及Cyp2e1基因敲除小鼠对乙酰氨基酚代谢的质量同位素异构体分析来鉴定新的毒性相关代谢物。
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Formation of 6-nitro-norepinephrine from nitric oxide and norepinephrine in the spinal cord and its role in spinal analgesia.
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Nitrite- and peroxide-dependent oxidation pathways of dopamine: 6-nitrodopamine and 6-hydroxydopamine formation as potential contributory mechanisms of oxidative stress- and nitric oxide-induced neurotoxicity in neuronal degeneration.
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Tetrahydrobiopterin inhibits monomerization and is consumed during catalysis in neuronal NO synthase.四氢生物蝶呤可抑制单体化,并在神经元型一氧化氮合酶的催化过程中被消耗。
J Biol Chem. 1999 Aug 27;274(35):24921-9. doi: 10.1074/jbc.274.35.24921.
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Crystal structure of constitutive endothelial nitric oxide synthase: a paradigm for pterin function involving a novel metal center.组成型内皮型一氧化氮合酶的晶体结构:涉及新型金属中心的蝶呤功能范例。
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Biosynthesis and action of nitric oxide in mammalian cells.哺乳动物细胞中一氧化氮的生物合成与作用
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Bright and dark sides of nitric oxide in ischemic brain injury.一氧化氮在缺血性脑损伤中的双刃剑作用。
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Nitric oxide influences dopaminergic processes.一氧化氮影响多巴胺能过程。
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Determination of nitric oxide synthase cofactors: heme, FAD, FMN, and tetrahydrobiopterin.
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Bioactive 6-nitronorepinephrine identified in mammalian brain.在哺乳动物大脑中鉴定出生物活性6-硝基去甲肾上腺素。
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10
Nitric oxide-induced nitration of catecholamine neurotransmitters: a key to neuronal degeneration?一氧化氮诱导的儿茶酚胺神经递质硝化作用:神经元变性的关键因素?
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6-硝基儿茶酚胺对神经元型一氧化氮合酶的抑制作用,一氧化氮与儿茶酚胺在氧化应激条件下的假定反应产物。

Inhibition of neuronal nitric oxide synthase by 6-nitrocatecholamines, putative reaction products of nitric oxide with catecholamines under oxidative stress conditions.

作者信息

Palumbo A, Astarita G, d'Ischia M

机构信息

Zoological Station 'Anton Dohrn', Villa Comunale, I-80121 Naples, Italy.

出版信息

Biochem J. 2001 May 15;356(Pt 1):105-10. doi: 10.1042/0264-6021:3560105.

DOI:10.1042/0264-6021:3560105
PMID:11336641
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1221817/
Abstract

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.

摘要

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。