Maternal deprivation affects behaviour from youth to senescence: amplification of individual differences in spatial learning and memory in senescent Brown Norway rats
Ms. Oitzl et al., Maternal deprivation affects behaviour from youth to senescence: amplification of individual differences in spatial learning and memory in senescent Brown Norway rats, EUR J NEURO, 12(10), 2000, pp. 3771-3780
Previous studies have shown that deprivation of the infant rat from materna
l care has pronounced effects on the stress system during ontogeny. Here we
test the hypothesis that 24 h of maternal deprivation at postnatal day 3 w
ill cause persistent changes in behaviour. Spatial learning and memory of m
ale Brown Norway rats deprived as infants were observed in the Morris water
maze at 3, 12, 24 and 30-32 months of age (young, adult, aged, senescent).
Their nondeprived mother-reared littermates served as controls. (i) With i
ncreasing age, water maze performance declined in deprived and nondeprived
groups. However, once the task was learned the animals maintained their goo
d performance during retest at later ages. (ii) Maternal deprivation delaye
d acquisition until adulthood and caused at every age a higher degree of pe
rsistent behaviour as judged from the performance of deprived rats' free sw
im trials and reversal trials. (iii) At senescence the mean performance in
the water maze did not differ between the groups. Instead, the individual p
erformance was strikingly different within each group. Senescent deprived r
ats were either nonimpaired or impaired with only a few animals showing an
intermediate performance. Thus, a large group of animals (approximate to 40
%) ages successfully as they are resistant to the effect of maternal depriv
ation. In contrast, the majority of the control animals displayed intermedi
ate performance. Taken together, maternal deprivation has life-long consequ
ences for behaviour and culminates at senescence in amplification of indivi
dual differences in learning ability rather than in a generalized deteriora
tion of cognitive functions.