Toronto Western Research Institute, Toronto Western Hospital, University Health Network, Toronto, Ontario M5T 2S8, Canada.
J Neurosci. 2011 May 11;31(19):7190-8. doi: 10.1523/JNEUROSCI.1171-11.2011.
l-3,4-dihydroxyphenylalanine (l-DOPA) is the most effective treatment for Parkinson's disease, but long-term l-DOPA administration is marred by the emergence of motor complications, namely, dyskinesia and a shortening of antiparkinsonian benefit (wearing-OFF). 3,4-methylenedioxymethamphetamine (MDMA) is unique in that it exerts antidyskinetic effects and may enhance antiparkinsonian actions of l-DOPA. MDMA is composed of two enantiomers with different pharmacological profiles; here, we describe a novel enantiospecific synthesis of the two enantiomers and expand on the previous characterization of their pharmacology. R-MDMA (rectus-MDMA) is relatively selective for 5-HT(2A) receptors, whereas S-MDMA (sinister-MDMA) inhibits both serotonin (SERT) and dopamine transporters (DAT; SERT/DAT ratio of 10 to 1). R- or S-MDMA (1, 3, and 10 mg/kg, s.c.) was administered in combination with l-DOPA (15 mg/kg, s.c.) to six female common marmosets (Callithrix jacchus) rendered parkinsonian by MPTP (1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine) administration. Motor disability, including parkinsonism and dyskinesia, and duration of antiparkinsonian benefit (ON-time) were evaluated. After the administration of R-MDMA (3 and 10 mg/kg), the severity of peak-dose dyskinesia was decreased (by 33 and 46%, respectively; p < 0.05); although total ON-time was unchanged (approximately 220 min), the duration of ON-time with disabling dyskinesia was decreased by 90 min when compared to l-DOPA alone (69% reduction; p < 0.05). S-MDMA (1 mg/kg) increased the total ON-time by 88 min compared to l-DOPA alone (34% increase; p < 0.05), though dyskinesia were exacerbated. These data suggest that racemic MDMA exerts simultaneous effects, reducing dyskinesia and extending ON-time, by 5-HT(2A) antagonism and SERT-selective mixed monoamine uptake inhibition, which arise from its R and S enantiomers, respectively.
L-3,4-二羟基苯丙氨酸(L-DOPA)是治疗帕金森病最有效的药物,但长期使用 L-DOPA 会导致运动并发症的出现,即运动障碍和抗帕金森病作用的缩短(开期缩短)。3,4-亚甲二氧基甲基苯丙胺(MDMA)的独特之处在于它具有抗运动障碍作用,并可能增强 L-DOPA 的抗帕金森病作用。MDMA 由两种具有不同药理学特征的对映异构体组成;在这里,我们描述了一种新的对映选择性合成这两种对映异构体的方法,并扩展了它们以前的药理学特征描述。R-MDMA(rectus-MDMA)对 5-HT2A 受体相对选择性,而 S-MDMA(sinister-MDMA)抑制 5-羟色胺(SERT)和多巴胺转运体(DAT;SERT/DAT 比值为 10 比 1)。R-或 S-MDMA(1、3 和 10 mg/kg,皮下注射)与 L-DOPA(15 mg/kg,皮下注射)联合给药,用于六只因 MPTP(1-甲基-4-苯基-1,2,3,6-四氢吡啶)给药而患有帕金森病的普通狨猴(Callithrix jacchus)。评估运动障碍,包括帕金森病和运动障碍,以及抗帕金森病作用的持续时间(ON 时间)。在给予 R-MDMA(3 和 10 mg/kg)后,峰值剂量运动障碍的严重程度降低(分别降低 33%和 46%;p<0.05);尽管总 ON 时间不变(约 220 分钟),但与单独给予 L-DOPA 相比,伴有致残性运动障碍的 ON 时间减少了 90 分钟(69%减少;p<0.05)。S-MDMA(1 mg/kg)与单独给予 L-DOPA 相比,总 ON 时间增加了 88 分钟(增加 34%;p<0.05),尽管运动障碍加剧。这些数据表明,外消旋 MDMA 通过 5-HT2A 拮抗作用和 SERT 选择性混合单胺摄取抑制作用,同时发挥作用,减少运动障碍并延长 ON 时间,这分别来自其 R 和 S 对映异构体。