The current status of pharmacotherapy for the treatment of Parkinson's disease: transition from single-target to multitarget therapy

被引:45
作者
Cheong, Siew L. [1 ]
Federico, Stephanie [2 ]
Spalluto, Giampiero [2 ]
Klotz, Karl-Norbert [3 ]
Pastorin, Giorgia [4 ]
机构
[1] Int Med Univ, Sch Pharm, Dept Pharmaceut Chem, Kuala Lumpur, Malaysia
[2] Univ Trieste, Dipartimento Sci Chim & Farmaceut, Trieste, Italy
[3] Univ Wurzburg, Inst Pharmakol & Toxikol, Wurzburg, Germany
[4] Natl Univ Singapore, Dept Pharm, Singapore, Singapore
关键词
MONOAMINE-OXIDASE-B; DOPAMINE AGONIST CHELATOR; ADENOSINE A(2A) RECEPTORS; DESIGNED MULTIPLE LIGANDS; ANTIPARKINSON AGENTS; DIFFERENTIAL ACTIONS; ALPHA-SYNUCLEIN; NEURODEGENERATIVE DISEASES; ANTAGONIST PROPERTIES; IN-VITRO;
D O I
10.1016/j.drudis.2019.05.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Parkinson's disease (PD) is a neurodegenerative disorder characterized by degeneration of dopaminergic neurons. Motor features such as tremor, rigidity, bradykinesia and postural instability are common traits of PD. Current treatment options provide symptomatic relief to the condition but are unable to reverse disease progression. The conventional single-target therapeutic approach might not always induce the desired effect owing to the multifactorial nature of PD. Hence, multitarget strategies have been proposed to simultaneously target multiple proteins involved in the development of PD. Herein, we provide an overview of the pathogenesis of PD and the current pharmacotherapies. Furthermore, rationales and examples of multitarget approaches that have been tested in preclinical trials for the treatment of PD are also discussed.
引用
收藏
页码:1769 / 1783
页数:15
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