The Glutamate Hypothesis: A Pathogenic Pathway from which Pharmacological interventions have Emerged

被引:31
作者
Veerman, S. R. T. [1 ]
Schulte, P. F. J. [2 ]
de Haan, L. [3 ]
机构
[1] Flexible Assert Community Treatment, Div Community Mental Hlth, Mental Hlth Serv Org North Holland North, NL-1813 KV Alkmaar, Netherlands
[2] Treatment Ctr Bipolar Disorders, Div Specialised Treatment, Mental Hlth Serv Org North Holland North, Alkmaar, Netherlands
[3] Acad Psychiat Ctr, Early Psychosis Dept, AMC, Amsterdam, Netherlands
关键词
schizophrenia; glutamate; NMDA receptor; clozapine; glycine; POSITIVE ALLOSTERIC MODULATORS; TREATMENT-RESISTANT SCHIZOPHRENIA; PLACEBO-CONTROLLED TRIAL; DOUBLE-BLIND; LY2140023; MONOHYDRATE; RATING-SCALE; ADD-ON; MEMANTINE; CLOZAPINE; ACTIVATION;
D O I
10.1055/s-0034-1383657
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We discuss the relevance of the glutamate hypothesis in explaining cognitive disturbances and negative symptoms in schizophrenia. 4 lines of evidence support the hypothesis that glutamate deregulation, mainly through dysfunction of the N-methyl-D-aspartate (NMDA) receptor, is an important underlying mechanism of schizophrenia. Glutamate pathways are promising sites for intervention. Glutamate agonists combined with non-clozapine antipsychotics and glutamate antagonists augmented to clozapine show interesting clinical benefits in refractory schizophrenia. We illustrate how unique properties of the NMDA receptor antagonist memantine in addition to clozapine, may cause improvement of positive, negative and cognitive symptoms of schizophrenia.
引用
收藏
页码:121 / 130
页数:10
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