Recent failures of new potential symptomatic treatments for Parkinson's disease: Causes and solutions

被引:27
作者
Linazasoro, G [1 ]
机构
[1] Ctr Neurol & Neurocirugia Func, Clin Quiron, San Sebastian 20012, Guipuzcoa, Spain
关键词
Parkinson's disease; motor complications; animal models; treatment alternatives;
D O I
10.1002/mds.20120
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
One major goal of current research in Parkinson's disease (PD) is the discovery of novel agents to improve symptomatic management. The object of these new treatments should be to provide effective symptom control throughout the course of the disease without the development of side effects such as motor and psychiatric complications. Results of several clinical trials of new treatment options reported in the past 2 years have shown negative or unsatisfactory results. Most of the drugs and surgical procedures used in these studies had been tested previously in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) monkeys as well as in the classic 6-hydroxydopamine-lesioned rat model. They raise several questions about the true reliability of animal studies, the adequacy of the working hypotheses and design of clinical trials, the validity of tools in current use to evaluate a specific effect, and the selectivity of the drugs used. All these factors may explain failure. This review focuses on pharmacological and surgical treatments tested to improve the management of patients with motor fluctuations and dyskinesias. Some of the recent trials and possible reasons for their lack of success are critically analysed. Finally, some suggestions to avoid further failures and improve results are proposed. (C) 2004 Movement Disorder Society.
引用
收藏
页码:743 / 754
页数:12
相关论文
共 122 条
[1]   Anatomical and physiological evidence for D1 and D2 dopamine receptor colocalization in neostriatal neurons [J].
Aizman, O ;
Brismar, H ;
Uhlén, P ;
Zettergren, E ;
Levey, AI ;
Forssberg, H ;
Greengard, P ;
Aperia, A .
NATURE NEUROSCIENCE, 2000, 3 (03) :226-230
[2]   Striatal fosB expression is causally linked with L-DOPA-induced abnormal involuntary movements and the associated upregulation of striatal prodynorphin mRNA in a rat model of Parkinson's disease [J].
Andersson, M ;
Hilbertson, A ;
Cenci, MA .
NEUROBIOLOGY OF DISEASE, 1999, 6 (06) :461-474
[3]  
[Anonymous], DECADE BRAIN
[4]  
Augood SJ, 2000, J COMP NEUROL, V421, P247
[5]   Adenosine A2A receptor antagonist treatment of Parkinson's disease [J].
Bara-Jimenez, W ;
Sherzai, A ;
Dimitrova, T ;
Favit, A ;
Bibbiani, F ;
Gillespie, M ;
Morris, MJ ;
Mouradian, MM ;
Chase, TN .
NEUROLOGY, 2003, 61 (03) :293-296
[6]  
Bara-Jimenez William, 2003, Neurology, V60, pA507
[7]   PARTIAL DOPAMINE AGONIST THERAPY OF LEVODOPA-INDUCED DYSKINESIAS [J].
BARONTI, F ;
MOURADIAN, MM ;
CONANT, KE ;
GIUFFRA, M ;
BRUGHITTA, G ;
CHASE, TN .
NEUROLOGY, 1992, 42 (06) :1241-1243
[8]   Experimental models of Parkinson's disease [J].
Beal, MF .
NATURE REVIEWS NEUROSCIENCE, 2001, 2 (05) :325-332
[9]   Neuroprotection for Parkinson's disease: a call for clinically driven experimental design [J].
Bezard, E .
LANCET NEUROLOGY, 2003, 2 (07) :393-393
[10]   Attenuation of levodopa-induced dyskinesia by normalizing dopamine D3 receptor function [J].
Bézard, E ;
Ferry, S ;
Mach, U ;
Stark, H ;
Leriche, L ;
Boraud, T ;
Gross, C ;
Sokoloff, P .
NATURE MEDICINE, 2003, 9 (06) :762-767