CHOLINERGIC MARKER DEFICITS INDUCED BY LESIONS OF THE NUCLEUS BASALISOF MEYNERT ARE ATTENUATED BY NERVE GROWTH-FACTOR IN YOUNG, BUT NOT INAGED, F344 RATS
Ac. Santucci et al., CHOLINERGIC MARKER DEFICITS INDUCED BY LESIONS OF THE NUCLEUS BASALISOF MEYNERT ARE ATTENUATED BY NERVE GROWTH-FACTOR IN YOUNG, BUT NOT INAGED, F344 RATS, Brain research, 609(1-2), 1993, pp. 327-332
To investigate the efficacy of nerve growth factor (NGF) in promoting
recovery from cholinergic damage, young (3-4 month old) and aged (22-2
3 month old) Fischer 344 rats received NMDA-induced unilateral lesions
of the nucleus basalis of Meynert and subcutaneous osmotic pumps (2-w
eek duration) connected to permanently implanted cannulas directed at
the lateral ventricle ipsilateral to the lesion. Pumps were filled wit
h either artificial CSF/rat serum albumin (the vehicle) or 5.0 mug of
angiotensin-free, beta-NGF. Fourteen days after surgery, all subjects
were sacrificed and their brains regionally dissected (frontal and occ
ipital cortices, striatum, and dorsal and ventral hippocampi) and assa
yed for choline acetyltransferase (CAT) and acetylcholinesterase (AChE
). Results indicated that the lesion decreased CAT and AChE levels wit
hin the frontal cortex of both young (29.8% and 39.4% depletion, respe
ctively) and aged (30.5% and 34.8% depletion, respectively) animals. O
nly in young animals did NGF reduce these lesion-induced CAT (by 34.2%
) and AChE deficits (by 65.5%). In fact, NGF exacerbated frontal corti
cal CAT depletions in aged animals in that percent depletion was 11.3%
more following treatment (30.5% vs. 41.8% depletion in Aged/CSF and A
ged/NGF groups, respectively). Lower CAT and AChE levels were found in
the striatum of aged animals, an effect not reversed by NGF treatment
. In contrast, NGF in young animals enhanced striatal CAT activity on
the non-lesioned side by 22.2%. Although NGF has previously been shown
to enhance the functional and structural status of cholinergic cells
in aged animals, the present data suggest that such an effect may not
apply to aged, cholinergically lesioned neurons or that treatment cond
itions (e.g. dose, duration of treatment, etc.), which are adequate fo
r promoting recovery in young adult rats, do not apply fully to aged r
ats.