Kassubek J, Büttner T, Reichmann H, Riederer P, Schulz J B, Wüllner U, Csoti I
Neurologische Klinik, Universität Ulm, Ulm.
Fortschr Neurol Psychiatr. 2010 Mar;78 Suppl 1:S34-6. doi: 10.1055/s-0029-1245166. Epub 2010 Mar 1.
In this workshop report, the N-methyl-D-aspartate (NMDA) receptor antagonists and the monoamine oxidase (MAO) type B inhibitors are discussed with respect to their role in the pharmacotherapy of Parkinson's Disease (PD). For the NMDA antagonist amantadine, studies demonstrated beneficial effects in various symptoms of the PD complex, while memantine seems to be beneficial in the treatment of cognitive deficits in PD-associated dementia. The MAO B inhibitors selegiline and rasagiline are in use for PD pharmacotherapy; for rasagiline, studies have demonstrated a possible disease-modifying effect. Although not supported by specific controlled studies, a "triple" early therapy is discussed which consists of a dopamine agonist, a MAO B inhibitor and amantadine, in order to try to delay the start of levodopa therapy.
在本研讨会报告中,就N-甲基-D-天冬氨酸(NMDA)受体拮抗剂和单胺氧化酶(MAO)B型抑制剂在帕金森病(PD)药物治疗中的作用进行了讨论。对于NMDA拮抗剂金刚烷胺,研究表明其对PD综合征的各种症状具有有益作用,而美金刚似乎对治疗PD相关性痴呆中的认知缺陷有益。MAO B抑制剂司来吉兰和雷沙吉兰用于PD的药物治疗;对于雷沙吉兰,研究已证明其可能具有疾病修饰作用。尽管没有具体对照研究的支持,但仍讨论了一种由多巴胺激动剂、MAO B抑制剂和金刚烷胺组成的“三联”早期治疗方法,以期尝试推迟左旋多巴治疗的开始。