Molecular basis of dopamine replacement therapy and its side effects in Parkinson's disease

被引:63
作者
You, Hana [1 ,2 ,3 ,4 ,5 ,6 ]
Mariani, Louise-Laure [1 ,2 ,3 ,4 ]
Mangone, Graziella [1 ,2 ,3 ,4 ]
de Nailly, Delphine Le Febvre [2 ,7 ]
Charbonnier-Beaupel, Fanny [7 ]
Corvol, Jean-Christophe [1 ,2 ,3 ,4 ,8 ]
机构
[1] UPMC Univ Paris 06, Sorbonne Univ, Hop Pitie Salpetriere, UMR S 1127,ICM, Paris, France
[2] Hop La Pitie Salpetriere, INSERM, Unit 1127, CIC 1422,NS PK FCRIN, Paris, France
[3] Hop La Pitie Salpetriere, CNRS, Unit 7225, Paris, France
[4] Hop La Pitie Salpetriere, AP HP, Dept Neurol, Paris, France
[5] Univ Hosp, Inselspital, Dept Neurol, Freiburgstr 18, CH-3010 Bern, Switzerland
[6] Univ Bern, Freiburgstr 18, CH-3010 Bern, Switzerland
[7] Hop La Pitie Salpetriere, AP HP, Dept Pharm, Paris, France
[8] Hop La Pitie Salpetriere, CIC Neurosci, ICM Bldg,47-83 Blvd Hop, F-75013 Paris, France
关键词
Parkinson's disease; Dopamine; Levodopa; Dopaminergic therapy; Dopamine signalling; IMPULSE CONTROL DISORDERS; CATECHOL-O-METHYLTRANSFERASE; LEVODOPA-INDUCED DYSKINESIAS; STIMULATED ADENYLYL-CYCLASE; MEDIUM SPINY NEURONS; GLUR1 AMPA RECEPTOR; DOUBLE-BLIND; MOTOR FLUCTUATIONS; NMDA RECEPTOR; LONG-TERM;
D O I
10.1007/s00441-018-2813-2
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
There is currently no cure for Parkinson's disease. The symptomatic therapeutic strategy essentially relies on dopamine replacement whose efficacy was demonstrated more than 50 years ago following the introduction of the dopamine precursor, levodopa. The spectacular antiparkinsonian effect of levodopa is, however, balanced by major limitations including the occurrence of motor complications related to its particular pharmacokinetic and pharmacodynamic properties. Other therapeutic strategies have thus been developed to overcome these problems such as the use of dopamine receptor agonists, dopamine metabolism inhibitors and non-dopaminergic drugs. Here we review the pharmacology and molecular mechanisms of dopamine replacement therapy in Parkinson's disease, both at the presynaptic and postsynaptic levels. The perspectives in terms of novel drug development and prediction of drug response for a more personalised medicine will be discussed.
引用
收藏
页码:111 / 135
页数:25
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