INVESTIGADORES
ABATE Paula
congresos y reuniones científicas
Título:
Interactions between pre- and postnatal ethanol experiences: Participation of Endogenous Opioid System upon newborn and infantile responsiveness to ethanol.
Autor/es:
MIRANDA-MORALES RS; MOLINA JC; ABATE P
Lugar:
Buenos Aires, Argentina
Reunión:
Congreso; 14th Biennial Scientific Meeting of the International Society for Comparative Psychology.; 2008
Institución organizadora:
International Society of Comparative Psychology
Resumen:
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Responsiveness to ethanols reinforcing
properties, mediated by the opioid system, is affected by early
experiences with the drug. In this study, we analyzed
the involvement of the Opioid System in the generation of pre- and postnatal
ethanol-related memories. We also evaluated alcohol self-administration in
newborn and infant rats as a function of such experience. Pregnant dams
received (GDs1720) one daily administration of ethanol (0 or 2g/kg) in
conjunction with naloxone (10mg/kg) or saline. On PD1, newborns were trained in
an operant task (FR=1) receiving ethanol or milk as reinforcers. Yoked-controls
received reinforcement with no contingence with its behavior. An extinction
session was also performed. Infantile intake of ethanol (5%v/v) was assessed
during PDs14 and 15. On PD14, before intake, pups received naloxone (1mg/kg) or
saline; a third group remained untreated. In the operant task, animals
belonging to prenatal ethanol groups and reinforced with ethanol, exhibited significantly
more resistance to extinction when comparing with the remaining groups. The
interaction between ethanol pre- and postnatal treatment resulted in heightened
ethanol intake scores (PD15). Intake scores were diminished by naloxone
administration (PD14). Nevertheless, prenatal naloxone failed to affect either,
neonatal or infantile Responsiveness to the drug. These
results support the hypothesis of a conditioned ethanol-preference acquired in
utero. Furthermore, ethanol experiences during gestation and nursing, promote
subsequent appetitive responses to the drug.