Kuhn D M
Department of Psychiatry and Behavioral Neurosciences, Wayne State University School of Medicine, Detroit, Michigan, USA.
Adv Exp Med Biol. 1999;467:19-27. doi: 10.1007/978-1-4615-4709-9_3.
Tryptophan hydroxylase is the initial and rate-limiting enzyme in the biosynthesis of the neurotransmitter serotonin. A variety of drugs are known to diminish the function of this enzyme, and possibly cause damage to serotonin neurons. These include the substituted amphetamines methamphetamine and 3,4-methylenedioxy-methamphetamine, as well as L-DOPA, the most common therapy for Parkinsons Disease. In view of the important role for dopamine in the effects of these drugs on tryptophan hydroxylase and on serotonin neurons, we tested whether dopamine could alter the activity of this important enzyme. We found that dopamine-derived quinones, but not dopamine, inactivate tryptophan hydroxylase and convert the protein to a redox-cycling quinoprotein. This posttranslational modification of tryptophan hydroxylase could play a role in the drug-induced reduction in serotonin synthesis.
色氨酸羟化酶是神经递质血清素生物合成中的起始和限速酶。已知多种药物会削弱这种酶的功能,并可能对血清素神经元造成损害。这些药物包括取代苯丙胺类的甲基苯丙胺和3,4-亚甲基二氧基甲基苯丙胺,以及治疗帕金森病最常用的左旋多巴。鉴于多巴胺在这些药物对色氨酸羟化酶和血清素神经元的作用中具有重要作用,我们测试了多巴胺是否会改变这种重要酶的活性。我们发现,源自多巴胺的醌类物质而非多巴胺会使色氨酸羟化酶失活,并将该蛋白质转化为一种氧化还原循环醌蛋白。色氨酸羟化酶的这种翻译后修饰可能在药物诱导的血清素合成减少中起作用。