Abstract
Parkinson’s disease is a progressive neurodegenerative disorder
resulting from the degeneration of pigmented dopaminergic neurons in the
substantia nigra pars compacta. It induces a series of functional
modifications in the circuitry of the basal ganglia nuclei and leads to
severe motor disturbances. The amino acid glutamate, as an excitatory
neurotransmitter, plays a key role in the disruption of normal basal
ganglia function regulated through the interaction with its receptor
proteins. It has been proven that glutamate receptors participate in the
modulation of neuronal excitability, transmitter release, and long-term
synaptic plasticity, in addition to being related to the altered
neurotransmission in Parkinson’s disease. Therefore, they are considered
new targets for improving the therapeutic strategies used to treat
Parkinson’s disease. In this review, we discuss the biological
characteristics of these receptors and demonstrate the receptor-mediated
neuroprotection in Parkinson’s disease. Pharmacological manipulation of
these receptors during anti-Parkinsonian processes in both experimental
studies and clinical trials are also summarized.
Original language | English |
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Article number | 4391 |
Number of pages | 17 |
Journal | International Journal of Molecular Sciences |
Volume | 20 |
Issue number | 18 |
DOIs | |
Publication status | Published - 6 Sept 2019 |
Scopus Subject Areas
- Catalysis
- Molecular Biology
- Spectroscopy
- Computer Science Applications
- Physical and Theoretical Chemistry
- Organic Chemistry
- Inorganic Chemistry
User-Defined Keywords
- Glutamate receptors
- MGluR4
- MGluR5
- NMDA receptor
- Parkinson’s disease