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The levels of the NMDA receptor co-agonist D-serine are reduced in the substantia nigra of MPTP-lesioned macaques and in the cerebrospinal fluid of Parkinson’s disease patients
- Source :
- Scientific Reports, Scientific Reports, Nature Publishing Group, 2019, 9 (1), ⟨10.1038/s41598-019-45419-1⟩, Scientific Reports, Vol 9, Iss 1, Pp 1-15 (2019)
- Publication Year :
- 2019
- Publisher :
- HAL CCSD, 2019.
-
Abstract
- Dysfunction of NMDA receptor (NMDAR)-mediated transmission is supposed to contribute to the motor and non-motor symptoms of Parkinson's Disease (PD), and to L-DOPA-induced dyskinesia. Besides the main agonist L-glutamate, two other amino acids in the atypical D-configuration, D-serine and D-aspartate, activate NMDARs. In the present work, we investigated the effect of dopamine depletion on D-amino acids metabolism in the brain of MPTP-lesioned Macaca mulatta, and in the serum and cerebrospinal fluid of PD patients. We found that MPTP treatment increases D-aspartate and D-serine in the monkey putamen while L-DOPA rescues both D-amino acids levels. Conversely, dopaminergic denervation is associated with selective D-serine reduction in the substantia nigra. Such decrease suggests that the beneficial effect of D-serine adjuvant therapy previously reported in PD patients may derive from the normalization of endogenous D-serine levels and consequent improvement of nigrostriatal hypoglutamatergic transmission at glycine binding site. We also found reduced D-serine concentration in the cerebrospinal fluid of L-DOPA-free PD patients. These results further confirm the existence of deep interaction between dopaminergic and glutamatergic neurotransmission in PD and disclose a possible direct influence of D-amino acids variations in the changes of NMDAR transmission occurring under dopamine denervation and L-DOPA therapy. Dysfunction of NMDA receptor (NMDAR)-mediated transmission is supposed to contribute to the motor and non-motor symptoms of Parkinson’s Disease (PD), and to L-DOPA-induced dyskinesia. Besides the main agonist L-glutamate, two other amino acids in the atypical D-configuration, D-serine and D-aspartate, activate NMDARs. In the present work, we investigated the effect of dopamine depletion on D-amino acids metabolism in the brain of MPTP-lesioned Macaca mulatta, and in the serum and cerebrospinal fluid of PD patients. We found that MPTP treatment increases D-aspartate and D-serine in the monkey putamen while L-DOPA rescues both D-amino acids levels. Conversely, dopaminergic denervation is associated with selective D-serine reduction in the substantia nigra. Such decrease suggests that the beneficial effect of D-serine adjuvant therapy previously reported in PD patients may derive from the normalization of endogenous D-serine levels and consequent improvement of nigrostriatal hypoglutamatergic transmission at glycine binding site. We also found reduced D-serine concentration in the cerebrospinal fluid of L-DOPA-free PD patients. These results further confirm the existence of deep interaction between dopaminergic and glutamatergic neurotransmission in PD and disclose a possible direct influence of D-amino acids variations in the changes of NMDAR transmission occurring under dopamine denervation and L-DOPA therapy.
- Subjects :
- 0301 basic medicine
Parkinson's disease
lcsh:Medicine
chemistry.chemical_compound
Mice
[SCCO]Cognitive science
0302 clinical medicine
Glycine binding
L-DOPA therapy
Serine
lcsh:Science
ComputingMilieux_MISCELLANEOUS
Multidisciplinary
MPTP
Putamen
Dopaminergic
Parkinson Disease
NMDA
3. Good health
Substantia Nigra
Settore MED/26 - NEUROLOGIA
medicine.drug
Agonist
medicine.medical_specialty
medicine.drug_class
Substantia nigra
Receptors, N-Methyl-D-Aspartate
Article
03 medical and health sciences
Dopamine
Internal medicine
medicine
Animals
Humans
business.industry
[SCCO.NEUR]Cognitive science/Neuroscience
lcsh:R
MPTP Poisoning
medicine.disease
030104 developmental biology
Endocrinology
chemistry
nervous system
Macaca
lcsh:Q
business
030217 neurology & neurosurgery
Neuroscience
Subjects
Details
- Language :
- English
- ISSN :
- 20452322
- Database :
- OpenAIRE
- Journal :
- Scientific Reports, Scientific Reports, Nature Publishing Group, 2019, 9 (1), ⟨10.1038/s41598-019-45419-1⟩, Scientific Reports, Vol 9, Iss 1, Pp 1-15 (2019)
- Accession number :
- edsair.doi.dedup.....459ce6224f65d25344565ef0f7a0be59