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