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B RIIT I S H J OU RN AL OF P SYCH IAT RY (2003), 1 83, 414

Size of hippocampal pyramidal neurons

in schizophrenia

J. R. HIGHLEY, M. A. WALKER, B. McDONALD, T. J. CROW and M. M. ESIRI


Background Meta-analyses of
hi
ppocampal size have indicated that this
st
ructure is smaller in schizophrenia.This
could
reflect a reduction in the size of
co
nstituent neurons or a reduced number
of n
eurons.

Aims To measure the size of
hippocampal pyramidal neurons in the
brains of people with and without
schizophrenia.

Method  Pyramidal neuron size in

hippocampal subfields was estimated
stereol
ogically from sections taken at
5 mm intervals throughout the whole
length of right and left hippocampi from
t
he brains of 13 people with schizophrenia
a
nd 16 controls. Results were assessed
us
ing repeated-measures analysis of
covariance looking for a main effect of
diagnosis and gender, and interactions of
these with side.

Results We were unable to detect
significant differences related to diagnosis,
ge
nder or side for any hippocampal
subfield for this series of cases.

Conclusions For this series of brains,
hi
ppocampal cell size is unchanged in
sch
izophrenia.

Declaration of interest None.
F
unding detailed in Acknowledgements.

The hippocampus has interested investiga-
to
rs into schizophrenia for many decades.
Experimental and human studies have
shown
its undoubted importance for mem-
ory
function, which is selectively impaired
in p
eople with schizophrenia (Gruzelier et
al
, 1988; Saykin et al, 1991; Gur et al,
1998). Furt
hermore, some structural ima-
ging st
udies of living patients, as well as
post
-mortem studies, report reductions in
hi
ppocampal size in schizophrenia (Bogerts
et al, 1985; Falkai & Bogerts, 1986; Jeste
& L
ohr, 1989; Nelson et al, 1998)-
although not all studies confirm this, per-
haps beca
use the numbers of individuals
st
udied were sometimes too low to detect
th
e quite subtle reductions described (Alt-
shule
r et al, 1990; Bruton et al, 1990;
H
eckers et al, 1990, 1991). The meta-
analy
sis of in vivo magnetic resonance ima-
ging
(MRI) studies by Nelson et al (1998)
in
dicated a reduction in hippocampal size
of appr
oximately 4%.

Reduction in size of a brain structure
m
ay reflect a reduced size of the constituent
glial
cells and neurons and their processes
as
well as (or as an alternative to) a reduced
num
ber of neurons. Thus, it is important to
document estimates of cell size as well as
cell num
ber in brain structures that are of
in
terest in schizophrenia. Here we present
our findings w
ith respect to pyramidal cell
volume, estimated stereologically, in the
hi
ppocampus on both sides of brains taken
fr
om 13 people with schizophrenia and 16
controls.

METHOD

The brains studied in this investigation
we
re a subset of 29 samples from a collec-
tio
n that has been described elsewhere
(H
ighley et al, 1999; McDonald et al,
2000; W
alker et al, 2002). In brief, brains
we
re collected post mortem from patients
wit
h schizophrenia and a control group,
and fixed b
y suspension in 10% formalin
solution. The case notes of the patients
a
nd controls were assessed by a psychiatrist
(
T.J.C. or Dr Stephen J. Cooper from
Q
ueen’s University, Belfast) to ensure that
they either fulfilled DSM-IV criteria for
s
chizophrenia or schizoaffective disorder
(
American Psychiatric Association, 1994),
or were free of psychopathological dis-
order. The next of kin gave consent for
u
se of brain tissue for research. All brains
w
ere examined by a neuropathologist
(B.M.), masked to diagnosis and gender,
who confirmed them as being free from
s
ignificant neuropathological changes. In
p
articular, there was no evidence of
c
erebrovascular disease, Alzheimer’s dis-
ease or Parkinson’s disease. All measures
w
ere made (by M.A.W.) masked to diag-
nosis and gender. The demographic details
o
f the brain donors in this study are given
in T
able 1.

The temporal lobes were dissected
a
way from the rest of the brain, and sliced
in
to 5 mm coronal slices throughout their
e
ntire length, such that the entirety of the
h
ippocampus was available for histological
examination. Each slice was embedded in
p
araffin wax, and a 25 mm section was
c
ut from its anterior face, mounted on a
c
oated slide, stained with cresyl violet
and luxol fast blue, and coverslipped.
The outlines of four cytoarchitecturally
defined hippocampal subfields were delin-
eated in the manner described by West &
G
undersen (1990):

(a) the hilus (CA4)

(b) an amalgamation of the CA2 and CA3
s
ubfields (hereafter CA2/3)

(c) the CA1 subfield

(d) the subiculum.

The volume density (Vv) of these subfields
w
as measured on both sides of the brain,
using stereological point-counting tech-
niques (Howard & Reed, 1998). Volume
density in this study refers to the proportion
o
f each hippocampal subfield that is
o
ccupied by pyramidal neuronal cell
bodies.

The prepared slides were examined
u
sing a 660 objective and an Olympus
B
X50 microscope mounted with a JVC
T
K-C1380 colour video camera and stage
motor, which in turn were controlled and
v
iewed on a computer running the Olym-
p
us Cast-Grid 2.0 stereology sampling soft-
w
are. On each slide, each subfield was
e
xamined at specific points positioned in a
r
aster search pattern array which covered

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