Ry. Shen et al., THE EFFECTS OF CHRONIC AMPHETAMINE TREATMENT ON PRENATAL ETHANOL-INDUCED CHANGES IN DOPAMINE-RECEPTOR FUNCTION - ELECTROPHYSIOLOGICAL FINDINGS, The Journal of pharmacology and experimental therapeutics, 274(3), 1995, pp. 1054-1060
The sensitivity of dopamine (DA) receptors in the mesoaccumbens DA sys
tem was investigated with extracellular recording and microiontophores
is techniques in adult rats that received prenatal ethanol exposure an
d chronic postnatal amphetamine treatment. Pregnant rats were fed with
a liquid diet containing 0 or 35% ethanol-derived calories from gesta
tion day 6 to 20. An ad libitum group received laboratory chow and wat
er. Off-spring were injected with amphetamine (2 mg/kg/day s.c.) or sa
line from postnatal day 22 to 10- to 12-months of age. Electrophysiolo
gical recording procedures were performed 16 to 24 hr after the last a
mphetamine injection. A supersensitivity of somatodendritic DA autorec
eptors in the ventral tegmental area was observed in animals exposed p
renatally to ethanol. This prenatal ethanol exposure-induced supersens
itivity was not observed after postnatal amphetamine treatment. In con
trol animals, postnatal amphetamine treatment did not affect the sensi
tivity of somatodendritic DA autoreceptors. The sensitivity of D-1 DA
receptors in the nucleus accumbens was reduced by prenatal ethanol exp
osure. Postnatal amphetamine treatment reduced D-1 DA receptor sensiti
vity in control animals, but not in animals exposed prenatally to etha
nol. Neither prenatal ethanol treatment nor postnatal amphetamine trea
tment altered the sensitivity of D-2 DA receptors in the nucleus accum
bens. There were no differences between the ad libitum and 0% ethanol-
derived calorie groups, indicating undernutrition did not affect DA re
ceptor function. These results show that prenatal ethanol exposure alt
ered DA receptor function in the mesoaccumbens DA system in adult anim
als. Furthermore, postnatal amphetamine treatment was able to eliminat
e the supersensitivity of somatodendritic DA autoreceptors in prenatal
ethanol-exposed animals.