D-Aspartate: An endogenous NMDA receptor agonist enriched in the developing brain with potential involvement in schizophrenia

被引:50
作者
Errico, Francesco [1 ,2 ]
Mothet, Jean-Pierre [3 ]
Usiello, Alessandro [1 ,4 ]
机构
[1] Ceinge Biotecnol Avanzate, Lab Behav Neurosci, I-80145 Naples, Italy
[2] Univ Naples Federico II, Dept Mol Med & Med Biotechnol, I-80138 Naples, Italy
[3] Aix Marseille Univ, CNRS, Ctr Rech Neurobiol & Neurophysiol Marseille, UMR7286, F-13344 Marseille 15, France
[4] Second Univ Naples SUN, Dept Environm Biol & Pharmaceut Sci & Technol, I-81100 Caserta, Italy
关键词
D-Aspartate; D-Serine; D-Aspartate oxidase; NMDA receptor; Schizophrenia; AMINO-ACID OXIDASE; LONG-TERM POTENTIATION; D-SERINE; L-GLUTAMATE; RAT-BRAIN; POSTNATAL CHANGES; NEURODEVELOPMENTAL HYPOTHESIS; SYNAPTIC PLASTICITY; DECREASED LEVELS; GLYCINE SITE;
D O I
10.1016/j.jpba.2015.03.024
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Free D-aspartate and D-serine occur at substantial levels in the mammalian brain. D-Serine is a physiological endogenous co-agonist for synaptic N-Methyl D-Aspartate (NMDA) receptors (NMDARs), and is involved in the pathophysiology of schizophrenia. Much less is known about the biological meaning of D-aspartate. D-Aspartate is present at high levels in the embryo brain and strongly decreases at post-natal phases. Temporal reduction of D-aspartate levels depends on the post-natal onset of D-aspartate oxidase (DDO), an enzyme able to selectively catabolize this D-amino acid. Pharmacological evidence indicates that D-aspartate binds to and activates NMDARs. Characterization of genetic and pharmacological mouse models with abnormally higher levels of D-aspartate has evidenced that increased D-aspartate enhances hippocampal NMDAR-dependent synaptic plasticity, dendritic morphology and spatial memory. In line with the hypothesis of a hypofunction of NMDARs in the pathogenesis of schizophrenia, it has been shown that increased D-aspartate levels also improve brain connectivity, produce corticostriatal adaptations resembling those observed after chronic haloperidol treatment, and protects against prepulse inhibition deficits and abnormal circuits activation induced by psychotomimetic drugs. In healthy humans, genetic variation predicting reduced expression of DDO in post-mortem prefrontal cortex is associated with greater prefrontal gray matter and activity during working memory. On the other side, evaluation of D-aspartate content in post-mortem patients with schizophrenia has shown a significant reduction of this D-amino acid in the prefrontal cortex and striatum. Generation of mouse models with reduced embryonic levels of D-aspartate may disclose unprecedented role for D-aspartate in developmental brain processes associated with vulnerability to psychotic-like symptoms. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:7 / 17
页数:11
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