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Published on: August 25, 2014
Prenatal and gestational cocaine exposure: Effects on the oxytocin system and social behavior with implications for
1Section on Neural Gene Expression, National Institute of Mental Health, Bethesda, MD, United States.
Insights
Prenatal cocaine exposure (PCE) in rats impairs social behaviors and disrupts oxytocin (Oxt) signaling. Maternal care deficits exacerbate these effects, highlighting drug abuse impacts on offspring development.
Area of Science:
- Neuroscience
- Developmental Psychology
- Toxicology
Background:
- Drug abuse during pregnancy poses significant public health risks, impacting offspring development.
- Prenatal cocaine exposure (PCE) in rats leads to social behavior deficits and altered neuroendocrine function.
- Maternal care is crucial for social development, and cocaine use during pregnancy disrupts this vital interaction.
Purpose of the Study:
- To investigate the distinct and combined effects of PCE and cocaine-induced maternal care deficits on social behaviors and oxytocin (Oxt) signaling in offspring.
- To understand the developmental trajectory of these effects from neonate to adulthood.
Main Methods:
- Utilized a rat model to study the effects of prenatal cocaine exposure (PCE).
- Assessed social behaviors, aggression, and oxytocin (Oxt) levels and mRNA expression in offspring.
- Examined the influence of rearing by cocaine-exposed mothers on offspring outcomes.
Main Results:
- PCE resulted in decreased social behaviors and increased aggression in adolescent and adult rats.
- Rearing by cocaine-exposed mothers exacerbated PCE-induced behavioral deficits.
- Maternal cocaine exposure, independent of PCE, altered Oxt signaling in specific brain regions, with dynamic effects observed in neonates.
Conclusions:
- Both PCE and disrupted maternal care contribute to social behavior deficits, with synergistic effects when combined.
- Oxytocin (Oxt) signaling is dynamically regulated early in development and is sensitive to both direct drug exposure and the early life environment.
- Understanding these interactions is crucial for addressing the long-term consequences of prenatal drug exposure and potential intergenerational transmission of addiction.
Abstract:
Drug abuse during pregnancy is a major public health concern, with negative consequences throughout development. Prenatal cocaine exposure (PCE) in rats produces social behavior deficits with corresponding changes in neuroendocrine and monoaminergic signaling. The relevance of parental care in social behavior maturity cannot be ignored, and gestational exposure to cocaine severely disrupts parental care, thus impacting the early environment of the offspring. Oxytocin (Oxt) is critical in regulating social behaviors and central levels are disrupted following acute and chronic cocaine (CC) treatment in postpartum rat dams, coincident with deficits in maternal care. We will discuss studies aimed to determine the relative contribution of PCE and CC-induced deficits in maternal care to social behaviors and Oxt signaling across development. PCE results in decreased social (including parental) behaviors in adolescence and adulthood. PCE is also associated with increased aggression in adults. Rearing by CC-exposed mothers synergistically increases the behavioral effects of PCE. Rearing by CC-exposed mothers, but not PCE, disrupts Oxt levels and mRNA in regions relevant to social behavior, but does not affect receptors in postpartum adult offspring. Preliminary work indicates that PCE/CC rearing has dynamic effects on Oxt levels and receptors in neonatal rat pups, suggesting very early regulation of Oxt signaling. This work highlights how the interactive role of Oxt signaling and behavioral context throughout development can be derailed by drug abuse during pregnancy. The relevance of disrupted Oxt to intergenerational transmission of addiction is briefly discussed.
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