Sulzer D, Zecca L
Department of Neurology, Columbia University, New York State Psychiatric Institute, New York, NY 10032, USA.
Neurotox Res. 2000 Feb;1(3):181-95. doi: 10.1007/BF03033289.
Dopamine-quinone is synthesized by oxidation of the catechol ring of dopamine. If this occurs within the neuronal cytosol, the quinone may react with cytosolic components, particularly with cysteine residues. In contrast, if quinone is produced within neuronal lysosomes it may provide the fundamental building block for neuromelanin. Since the population of neurons that die in Parkinson's disease are those that display obvious intralysosomal neuromelanin and since cytosolic dopamine-dependent oxyradical formation may underlie methamphetamine toxicity and other specific forms of neurodegeneration in dopaminergic neurons, it is important to elucidate the pathways leading to production of dopamine-quinone. Here we review pathways by which intracellular catechols may be oxidized to quinones, either enzymatically or via reduction of ferric iron or other metals. These metabolites can be adduced by cysteine, could underlie aberrant metabolism and ubiquitination pathways, may induce Lewy body formation, and mediate the synthesis of hydroxyl radical and oxyradical species. Finally, we suggest that by accumulating excess cytosolic catecholamine, neuromelanin synthesis may safely sequester quinones that would otherwise be produced in the neuronal cytosol.
多巴胺醌是通过多巴胺儿茶酚环的氧化合成的。如果这种情况发生在神经元胞质溶胶中,醌可能会与胞质成分发生反应,特别是与半胱氨酸残基反应。相反,如果醌在神经元溶酶体内产生,它可能为神经黑色素提供基本构建单元。由于在帕金森病中死亡的神经元群体是那些显示出明显的溶酶体内神经黑色素的神经元,并且由于胞质多巴胺依赖性氧自由基的形成可能是甲基苯丙胺毒性和多巴胺能神经元中其他特定形式神经退行性变的基础,因此阐明导致多巴胺醌产生的途径很重要。在这里,我们综述了细胞内儿茶酚可能通过酶促作用或通过三价铁或其他金属的还原而氧化为醌的途径。这些代谢产物可以被半胱氨酸诱导,可能是异常代谢和泛素化途径的基础,可能诱导路易小体形成,并介导羟自由基和氧自由基的合成。最后,我们认为,通过积累过量的胞质儿茶酚胺,神经黑色素的合成可能会安全地隔离那些否则会在神经元胞质溶胶中产生的醌。