S. Dracheva et al., N-methyl-D-aspartic acid receptor expression in the dorsolateral prefrontal cortex of elderly patients with schizophrenia, AM J PSYCHI, 158(9), 2001, pp. 1400-1410
Objective: The N-methyl-D-aspartic acid (NMDA) class of glutamate receptors
has received attention in the pathophysiology of schizophrenia because of
the similarity between some schizophrenic symptoms and symptoms caused by N
MDA antagonists. To determine if NMDA receptor abnormalities were present a
t the mRNA level, expression of NMDA receptor (NR) subunits NR1, NR2A, and
NR2B Was measured in specimens from the dorsolateral prefrontal cortex and
the occipital cortex of elderly patients with schizophrenia and normal elde
rly subjects.
Method: Postmortem specimens from antemortem assessed and diagnosed elderly
patients with schizophrenia (N=26) were compared with those from a neuropa
thologically and neuropsychiatrically normal elderly comparison group (N=13
) and from patients with Alzheimer's disease (N=10). The mRNA expression of
the NR1, NR2A, and NR2B subunits and of postsynaptic density 95 (PSD-95),
a protein associated with postsynaptic NMDA receptors, was studied with qua
ntitative real-time reverse transcriptase polymerase chain reaction.
Results: Expression of NR1 and NR2A but not NR2B subunits was higher in the
dorsolateral prefrontal cortex and the occipital cortex of patients with s
chizophrenia than in the normal and Alzheimer's disease groups. In contrast
, NR1 expression was significantly lower in the Alzheimer's disease group.
Occipital cortex expression of PSD-95 was higher in the schizophrenic subje
cts and correlated strongly with the expression of NR2A and NR2B in both co
rtical regions and with expression of NR1 in the occipital cortex, These re
sults were not influenced by neuroleptic exposure history, postmortem inter
val, or age of the subject,
Conclusions: NMDA receptor subunits are abnormally expressed in elderly pat
ients with schizophrenia, The disproportionate expression of the NR1 and NR
2A subunits relative to NR2B expression may have implications for the patho
physiology of schizophrenia and the sensitivity of schizophrenic patients t
o glutamate and glutamatergic drugs.