Gille G, Rausch W D, Hung S T, Moldzio R, Ngyuen A, Janetzky B, Engfer A, Reichmann H
Department of Neurology, Technical University of Dresden, Federal Republic of Germany.
J Neural Transm (Vienna). 2002 Feb;109(2):157-69. doi: 10.1007/s007020200011.
Dopamine agonists play an important role in the treatment of Parkinson's disease by reducing the administration of L-3,4-dihydroxyphenylalanine (L-DOPA). The enzymatic and non-enzymatic conversion of L-DOPA is suspected to increase oxidative stress, which leads to the degeneration of dopaminergic neurons in Parkinson's disease. In primary mouse mesencephalic cultures we show that the dopamine D1/D2 receptor agonist lisuride, in a concentration range of 0.001-1 microM, enhances the survival of dopaminergic neurons, protects against toxicity induced by L-DOPA or 1-methyl-4-phenylpyridinium ion (MPP+) and stimulates 3H-dopamine uptake. Lisuride also reduces anaerobic metabolism during incubation with L-DOPA. The present findings suggest that lisuride may have trophic/survival-promoting properties and potentially reduces oxidative stress.
多巴胺激动剂通过减少左旋多巴(L-3,4-二羟基苯丙氨酸,L-DOPA)的用量,在帕金森病的治疗中发挥重要作用。L-DOPA的酶促和非酶促转化被怀疑会增加氧化应激,进而导致帕金森病中多巴胺能神经元的退化。在原代小鼠中脑培养物中,我们发现多巴胺D1/D2受体激动剂利苏力特在0.001 - 1微摩尔的浓度范围内,可提高多巴胺能神经元的存活率,保护细胞免受L-DOPA或1-甲基-4-苯基吡啶离子(MPP+)诱导的毒性,并刺激3H-多巴胺摄取。利苏力特在与L-DOPA共同孵育期间还可减少无氧代谢。目前的研究结果表明,利苏力特可能具有营养/促进存活的特性,并有可能降低氧化应激。