Department of Physiology, University of Tartu, Tartu, Estonia.
Dermatology. 2012;224(2):168-76. doi: 10.1159/000338023. Epub 2012 May 4.
Dopamine has been proven to be toxic for melanocytes. In vitiligo patients the level of dopamine is increased and the functioning of several enzymes participating in the dopamine pathway is changed.
With the use of quantitative real-time polymerase chain reaction and ELISA the expression of genes connected to the dopamine pathway (PAH, PCD, TH, DDC, DBH, PNMT, GPX1, MAOA, MAOB, COMT, DRD1-DRD5, VMAT1 and VMAT2) was observed in vitiligo patients' and control subjects' skin and blood.
The mRNA expression of GPX1, DDC, MAOA, DRD1 and DRD5 differs in vitiligo skin and the protein level of DDC, MAOA, MAOB, DRD1 and DRD5 is changed in vitiligo patients' skin and/or blood sera.
The dopamine pathway probably influences melanogenesis directly or through the melanocortin pathway. We provide new data about changes of expression profile of the dopamine-synthesizing enzyme DDC, the dopamine-degrading enzymes MAOA and MAOB and the D1-like family dopamine receptors in vitiligo skin and blood sera.
多巴胺已被证明对黑素细胞有毒性。在白癜风患者中,多巴胺水平升高,参与多巴胺途径的几种酶的功能发生改变。
使用定量实时聚合酶链反应和 ELISA,观察白癜风患者和对照组皮肤和血液中与多巴胺途径(PAH、PCD、TH、DDC、DBH、PNMT、GPX1、MAOA、MAOB、COMT、DRD1-DRD5、VMAT1 和 VMAT2)相关的基因表达。
白癜风皮肤中 GPX1、DDC、MAOA、DRD1 和 DRD5 的 mRNA 表达不同,白癜风患者皮肤和/或血清中 DDC、MAOA、MAOB、DRD1 和 DRD5 的蛋白水平发生改变。
多巴胺途径可能直接或通过黑素皮质素途径影响黑色素生成。我们提供了关于白癜风皮肤和血清中多巴胺合成酶 DDC、多巴胺降解酶 MAOA 和 MAOB 以及 D1 样家族多巴胺受体表达谱变化的新数据。