Neonatal rat pups exposed to repetitive acute pain show decreases in pain t
hreshold and altered behavior during adulthood. A model using prolonged inf
lammatory pain in neonatal rats may have greater clinical relevance for inv
estigating the long-term behavioral effects of neonatal pain in ex-preterm
neonates. Neonatal rat pups were exposed to repeated formalin injections on
postnatal (P) days 1-7 (P1-P7), with or without morphine pretreatment, and
were compared with untreated controls. Behavioral testing during adulthood
assessed pain thresholds using hot-plate (HP) and tail-flick (TF) tests, a
lcohol preference, and locomotor activity (baseline and post-amphetamine).
Adult rats exposed to neonatal inflammatory pain exhibited longer HP latenc
ies than controls and male rats had longer HP thresholds compared to female
s. Male rats exposed to neonatal morphine alone exhibited longer TF latenci
es than controls. Both neonatal morphine treatment and neonatal inflammator
y pain decreased ethanol preference, but their effects were not additive. D
uring adulthood, male rats exposed to neonatal inflammatory pain exhibited
less locomotor activity than untreated controls. We conclude that neonatal
formalin and morphine treatment have specific patterns of long-term behavio
ral effects in adulthood, some of which are attenuated when the two treatme
nts are combined. (C) 2001 Elsevier Science Inc. All rights reserved.