Effects of acute ethanol intoxication during pregnancy on central dopaminergic system in male rats

• Published in: Neurotoxicology and teratology Vol. 16; no. 4; p. 385
• Main Authors: Fulginiti, S, Minetti, S A, Virgolini, M B
• Format: Journal Article
• Language: English
• Published: United States 01.07.1994
• Subjects: 3,4-Dihydroxyphenylacetic Acid - metabolism; Aging - metabolism; Alcoholic Intoxication; Amphetamine - pharmacology; Animals; Apomorphine - pharmacology; Corpus Striatum - drug effects; Corpus Striatum - growth & development; Corpus Striatum - metabolism; Dopamine - metabolism; Dose-Response Relationship, Drug; Female; Gestational Age; Male; Motor Activity - drug effects; Nucleus Accumbens - drug effects; Nucleus Accumbens - growth & development; Nucleus Accumbens - metabolism; Pregnancy; Prenatal Exposure Delayed Effects; Rats; Rats, Wistar; Stereotyped Behavior - drug effects; Synapses - drug effects; Synapses - metabolism
• ISSN: 0892-0362
• DOI: 10.1016/0892-0362(94)90027-2

Pregnant albino rats received 2 IP injections, spaced by 4 h, of either ethanol (2.9 g/kg in 24% v/v saline solution) or saline, on gestational day (GD) 8. During adulthood, male rats prenatally exposed to alcohol exhibited an increased stereotyped behavioral response to 12 mg/kg of amphetamine (AMPH) or 1 mg/kg of apomorphine (APO), whereas the stereotypy induced by 6 mg/kg of AMPH showed no difference between control and experimental animals. Also, the hypoactivity response elicited by small doses of APO was not significantly affected by the prenatal treatment with alcohol. Analysis of dopaminergic function in the striatum and nucleus accumbens demonstrated no change on dopamine (DA) levels in both structures in alcohol pre-exposed 55- and 180-day-old rats. A reduction in striatum 3-4 dihydroxyphenylacetic acid levels was observed at both ages. These results indicate that an acute intoxication with alcohol on GD 8 induces a long-lasting decrease in striatal but not in nucleus accumbens DA metabolism. As a consequence, a lower striatal DA release might produce a compensatory supersensitivity of postsynaptic DA sites. This interpretation is consistent and correlates with behavioral results.