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Brain NMDA Receptors in Schizophrenia and Depression
被引:160
作者:
Adell, Albert
[1
,2
]
机构:
[1] Univ Cantabria, Inst Biomed & Biotechnol Cantabria, IBBTEC, CSIC, Calle Albert Einstein 22 PCTCAN, Santander 39011, Spain
[2] Biomed Res Networking Ctr Mental Hlth CIBERSAM, Santander 39011, Spain
关键词:
NMDA;
depression;
schizophrenia;
subunit;
glutamate;
GABA;
METHYL-D-ASPARTATE;
MEDIAL PREFRONTAL CORTEX;
MTOR SIGNALING PATHWAY;
INDUCED DOPAMINE RELEASE;
PLACEBO-CONTROLLED TRIAL;
EXCITATORY AMINO-ACIDS;
MESSENGER-RNA LEVELS;
PREPULSE INHIBITION;
GENE-EXPRESSION;
D-CYCLOSERINE;
D O I:
10.3390/biom10060947
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
N-methyl-D-aspartate (NMDA) receptor antagonists such as phencyclidine (PCP), dizocilpine (MK-801) and ketamine have long been considered a model of schizophrenia, both in animals and humans. However, ketamine has been recently approved for treatment-resistant depression, although with severe restrictions. Interestingly, the dosage in both conditions is similar, and positive symptoms of schizophrenia appear before antidepressant effects emerge. Here, we describe the temporal mechanisms implicated in schizophrenia-like and antidepressant-like effects of NMDA blockade in rats, and postulate that such effects may indicate that NMDA receptor antagonists induce similar mechanistic effects, and only the basal pre-drug state of the organism delimitates the overall outcome. Hence, blockade of NMDA receptors in depressive-like status can lead to amelioration or remission of symptoms, whereas healthy individuals develop psychotic symptoms and schizophrenia patients show an exacerbation of these symptoms after the administration of NMDA receptor antagonists.
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页码:1 / 27
页数:27
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