Microtubule associated proteins (MAPs) are central to the development of no
rmal neuronal cytoarchitecture and have been reported to be altered in schi
zophrenia. In 12 schizophrenic (DSM-III-R criteria) and 12 control hippocam
pi, we estimated the MAP2 immunoreactive dendritic length using antibodies
that recognize total MAP2 (MAP2-T), and a non-phosphorylated form of MAP2 (
MAP2-NP). Within the corona ammonis (CA) subregions, and the subiculum, we
estimated, for each antibody, the length of the immunoreactive dendritic ar
borisation using a stereological length estimation technique based on Bouff
on's Needle principle and image analysis computer software. Controlling for
the confounding effects of age and post-mortem delay, we have found an ele
vation in overall MAP2-NP immunoreactive dendritic length among schizophren
ic subjects in the CA3 (F = 5.9, p = 0.03), CA2 (F = 6.5, p = 0.02), CA1 (F
= 8.3, p = 0.01) and subicular (F = 9.5, p = 0.008) hippocampal subregions
. Similar analyses of MAP2-T immunoreactive dendritic length demonstrated s
ignificant elevations in the CA1 (F = 8.3, p = 0.02), CA4 (F = 4.9, p = 0.0
4) and subicular (F = 7.4, p = 0.01) regions.
The findings of this quantitative study of increased MAP2 immunoreactive de
ndritic arborisation in schizophrenia are most likely to reflect either an
altered dendritic arborisation or a generalised increase in levels of MAP2
with the hippocampal pyramliteratureidal neurons. These findings add to the
growing indicating the presence of synaptodendritic abnormalities in schiz
ophrenia. (C) 2000 Elsevier Science B.V. All rights reserved.