Numerical changes in the overall neostriatal neuronal population have
been investigated by morphometric analysis of Nissl-stained and glucoc
orticoid receptor-immunoreactive neurons. Number and staining intensit
y of various chemically-identified nerve cell populations were analyse
d by means of immunocytochemistry coupled with computer-assisted image
analysis. Three- and 24-month-old male Sprague-Dawley rats were used.
No change in the number of Nissl-stained, glucocorticoid receptor-, d
opamine and adenosine 3':5'-monophosphate-regulated phosphoprotein- an
d enkephalin-immunoreactive neurons and a 50% decrease of neuropeptide
Y-immunoreactive neurons were observed in the aged rat. In our prepar
ations. the glucocorticoid receptor antibody stains around 90% of the
neostriatal neurons, the dopamine and adenosine 3':5'-monophosphate-re
gulated phosphoprotein and enkephalin antibodies label 25-35% and the
neuropeptide Y- antibody stains only 1% of neostriatal neurons. In the
same preparations a significant decrease in the intensity of immunost
aining was observed for enkephalin-, dopamine and adenosine 3':5'-mono
phosphate-regulated phosphoprotein- and neuropeptide Y-immunoreactive
neuronal cell bodies and tyrosine hydroxylase-immunoreactive nerve ter
minals in the aged rat. In the case of neuropeptide Y-, and dopamine a
nd adenosine 3':5'-monophosphate-regulated phosphoprotein-immunoreacti
ve neurons, the changes in the intensity of immunostaining were differ
entially compartmentalized within neostriatum, suggesting selective vu
lnerability of striatal subregions to ageing processes. In conclusion,
these data indicate that no significant age-related neuronal cell los
s occurs in neostriatum. On the other hand, a generalized decrease in
the levels of peptide transmitters and molecules related to dopamine t
ransmission is observed in aged rat neostriatum, possibly resulting in
the known age-related deficits of neostriatally-controlled behaviours
.