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Nucleic Acid-Based Therapeutics for Parkinson's Disease
被引:40
|作者:
Nakamori, Masayuki
[1
]
Junn, Eunsung
[2
,3
]
Mochizuki, Hideki
[1
]
Mouradian, M. Maral
[2
,3
]
机构:
[1] Osaka Univ, Grad Sch Med, Dept Neurol, Suita, Osaka, Japan
[2] Rutgers Biomed & Hlth Sci, Robert Wood Johnson Med Sch Inst Neurol Therapeut, Piscataway, NJ 08854 USA
[3] Rutgers Biomed & Hlth Sci, Dept Neurol, Piscataway, NJ 08854 USA
基金:
美国国家卫生研究院;
关键词:
alpha-Synuclein;
Antisense oligonucleotides;
MicroRNA;
Gene therapy;
Neurodegeneration;
ALPHA-SYNUCLEIN EXPRESSION;
GENE-THERAPY;
SUBSTANTIA-NIGRA;
ANTISENSE OLIGONUCLEOTIDES;
DOWN-REGULATION;
DOUBLE-BLIND;
NEURODEGENERATIVE DISEASES;
SILENCING VECTOR;
DOPAMINE NEURONS;
SIRNA DELIVERY;
D O I:
10.1007/s13311-019-00714-7
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Parkinson's disease (PD) is a progressive neurodegenerative disorder that is diagnosed largely on clinical grounds due to characteristic motor manifestations that result from the loss of nigrostriatal dopaminergic neurons. While traditional pharmacological approaches to enhance dopamine levels, such as with l-dopa, can be very effective initially, the chronic use of this dopamine precursor is commonly plagued with motor response complications. Additionally, with advancing disease, non-motor manifestations emerge, including psychosis and dementia that compound patient disability. The pathology includes hallmark intraneuronal inclusions known as Lewy bodies and Lewy neurites that contain fibrillar -synuclein aggregates. Evidence has also accumulated that these aggregates can propagate across synaptically connected brain regions, a phenomenon that can explain the progressive nature of the disease and the emergence of additional symptoms over time. The level of -synuclein is believed to play a critical role in its fibrillization and aggregation. Accordingly, nucleic acid-based therapeutics for PD include strategies to deliver dopamine biosynthetic enzymes to boost dopamine production or modulate the basal ganglia circuitry in order to improve motor symptoms. Delivery of trophic factors that might enhance the survival of dopamine neurons is another strategy that has been attempted. These gene therapy approaches utilize viral vectors and are delivered stereotaxically in the brain. Alternative disease-modifying strategies focus on downregulating the expression of the -synuclein gene using various techniques, including modified antisense oligonucleotides, short hairpin RNA, short interfering RNA, and microRNA. The latter approaches also have implications for dementia with Lewy bodies. Other PD genes can also be targeted using nucleic acids. In this review, we detail these various strategies that are still experimental, and discuss the challenges and opportunities of nucleic acid-based therapeutics for PD.
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页码:287 / 298
页数:12
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