NEUROPROTECTION AGAINST NMDA INDUCED CELL-DEATH IN RAT NUCLEUS BASALIS BY CA2-TREATMENT( ANTAGONIST NIMODIPINE, INFLUENCE OF AGING AND DEVELOPMENTAL DRUG)

Citation
Pgm. Luiten et al., NEUROPROTECTION AGAINST NMDA INDUCED CELL-DEATH IN RAT NUCLEUS BASALIS BY CA2-TREATMENT( ANTAGONIST NIMODIPINE, INFLUENCE OF AGING AND DEVELOPMENTAL DRUG), Neurodegeneration, 4(3), 1995, pp. 307-314
Citations number
54
Categorie Soggetti
Neurosciences
Journal title
ISSN journal
10558330
Volume
4
Issue
3
Year of publication
1995
Pages
307 - 314
Database
ISI
SICI code
1055-8330(1995)4:3<307:NANICI>2.0.ZU;2-Q
Abstract
In the current study the neuroprotective effect of the L-type calcium channel antagonist nimodipine in rat brain was investigated in N-methy l-D-aspartate-induced neuronal degeneration in vivo. In the present mo del NMDA was unilaterally injected in the magnocellular nucleus basali s and the neurotoxic impact assessed by measuring cortical cholinergic fibre loss as a percentage of fibre density of the intact control hem isphere. This procedure proved to be a reproducible model in which the degree of damage was almost linearly proportional to the NMDA dose. N europrotection by nimodipine was determined in a number of conditions. First, the effect of nimodipine treatment in adult animals starting t wo weeks prior to neurotoxic injury was compared with neuroprotection provided by perinatal treatment of the mother animals with the calcium antagonist. Surprisingly, the degree of protection was in both cases similar, yielding almost 30% reduction of fibre loss. The neuroprotect ive effect in adulthood of perinatal nimodipine treatment may be expla ined by developmentally enhanced calcium binding proteins or persisten t developmental changes in calcium channel characteristics. Protection by nimodipine was also investigated in aged, 26 month old rats. Compa red to young adult cases, aged animals proved to be less vulnerable to NMDA exposure, while nimodipine application was more potent, thus yie lding a reduction of nearly 50% in nerve fibre damage induced by NMDA infusions. Possible mechanisms of differential calcium influx in the v arious experimental conditions will be discussed. (C) 1995 Academic Pr ess Limited