W. Reimann et al., EFFECTS OF AGING AND LONG-TERM OPERANT-CONDITIONING ON BEHAVIOR AND PRESYNAPTIC CHOLINERGIC AND DOPAMINERGIC NEURONAL MECHANISMS IN RATS, Archives internationales de pharmacodynamie et de therapie, 325, 1993, pp. 5-20
Presynaptic events in the brain, such as neurotransmitter synthesis an
d release, may change during ageing or by performance of an operant be
havior. Therefore, we measured the acetylcholine synthesis and release
, and the dopamine release in brain tissue from different groups of ra
ts. Male Sprague-Dawley rats, 4-5 or 16-17 months old, were housed ind
ividually under identical conditions; one group of the older rats was
maintained under an operant conflict procedure for 8 months. Striatal
and cerebral cortex slices were preincubated with [H-3]dopamine and [H
-3]choline, respectively, superfused and stimulated electrically. Diff
erent Ca++ concentrations were used and, in [H-3]dopamine experiments,
0.1 mumol/l of apomorphine was added. Hippocampal slices were incubat
ed with [H-3]choline, and H-3-uptake and [H-3]acetylcholine synthesis
were measured. Gross behavior was not different between the groups as
regards duration of exploration, defecation rate or spontaneous motili
ty. Uptake of [H-3]choline and synthesis of [H-3]acetylcholine tended
to be lower in the aged rats but did not differ significantly in the g
roups. The [H-3]dopamine release was significantly reduced by 20 % in
aged rats as compared to young or aged, trained rats. The effect of ch
anges in Ca++ concentration and the response to apomorphine on the rel
ease of [H-3]dopamine were similar in all groups, indicating a lack of
age-related changes of the N-type Ca++ channels and presynaptic D-2 r
eceptors. Thus, ageing coincided with an impaired striatal dopamine re
lease which was prevented by the operant conditioning.