Jw. Unger et Y. Schmidt, NEUROPEPTIDE-Y AND SOMATOSTATIN IN THE NEOCORTEX OF YOUNG AND AGING RATS - RESPONSE TO NUCLEUS BASALIS LESIONS, Journal of chemical neuroanatomy, 7(1-2), 1994, pp. 25-34
Lesions of the nucleus basalis of Meynert (NBM) have been used to mimi
c, in part, cholinergic deficits occurring in age-related neurodegener
ative disorders, i.e., Alzheimer's disease. In our study, the effect o
f a persistent cholinergic denervation of the frontoparietal cortex on
neuropeptide Y (NPY) and somatostatin (SOM) was examined in young adu
lt (3 months old) and aging(>18 months old) rats, 1, 3 and 6 months af
ter bilateral stereotaxic NBM lesions with quisqualic acid. In aging,
non-lesioned rats a significant decrease in radioimmunologically and i
mmunohistochemically detectable NPY and SOM was found with no further
changes after lesions. Morphological markers for these peptidergic pop
ulations (cell size and number, NADPH-diaphorase histochemistry, elect
ron microscopy) demonstrated no signs of alterations in both age group
s after lesion. Densitometric analysis of peptide fibre networks displ
ayed a heterogeneous response with a significant rarefication in young
rats 1 month after the lesion, followed by restoration and a tendency
towards increase 6 months post lesioning in individual animals. These
findings were confirmed by radioimmunological measurements. Examinati
on of synaptic and cytoskeletal markers, i.e., synaptophysin, GAP-43,
MAP-2, Tau-l and amyloid precursor protein, did not reveal any signs f
or neuronal reorganization or sprouting. These data are discussed in t
he context of plasticity and pathology in age-related neurodegenerativ
e disorders with cholinergic impairment.