CHOLINERGIC MARKER DEFICITS INDUCED BY LESIONS OF THE NUCLEUS BASALISOF MEYNERT ARE ATTENUATED BY NERVE GROWTH-FACTOR IN YOUNG, BUT NOT INAGED, F344 RATS

Citation
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
Citations number
38
Categorie Soggetti
Neurosciences
Journal title
ISSN journal
00068993
Volume
609
Issue
1-2
Year of publication
1993
Pages
327 - 332
Database
ISI
SICI code
0006-8993(1993)609:1-2<327:CMDIBL>2.0.ZU;2-C
Abstract
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.