Effects of prenatal cocaine exposure on estrous cycle, and behavior and expression of estrogen receptor alpha and oxytocin during estrus and diestrus in mice offspring
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Summary
This summary is machine-generated.Prenatal cocaine exposure alters female offspring
Area Of Science
- Neuroscience
- Developmental Biology
- Reproductive Science
Background
- Prenatal cocaine exposure (PCE) is linked to long-term neurological and behavioral deficits.
- Female behaviors are influenced by the estrous cycle, with estrogen receptors and oxytocin playing key roles in social behavior regulation.
- The impact of PCE on the estrous cycle and subsequent neurobehavioral outcomes in female offspring remains largely unexplored.
Purpose Of The Study
- To investigate whether PCE induces changes in the estrous cycle of female offspring.
- To compare neurobehavioral changes (locomotion, anxiety, social behavior) in PCE offspring during different estrous cycle phases (estrus vs. diestrus).
- To examine the expression of estrogen receptor alpha (ERα) and oxytocin in the brains of PCE offspring.
Main Methods
- Mice received daily cocaine administration during gestation (gestational day 12 for 7 days).
- Adult female offspring underwent estrous cycle assessment.
- Locomotion, anxiety, social behaviors, and ERα/oxytocin neuron expression were evaluated, comparing estrus and diestrus phases.
Main Results
- PCE shortened the proestrus and estrus phases of the estrous cycle.
- PCE offspring exhibited increased anxiety and altered social behaviors during both estrus and diestrus.
- Motility was unaffected in estrus but reduced in diestrus; ERα and oxytocin expression decreased in specific brain regions.
Conclusions
- PCE disrupts the estrous cycle and alters ERα and oxytocin expression in a region-specific manner.
- PCE and the estrous cycle interact to influence offspring motility and social behaviors.
- ERα and oxytocin signaling pathways are implicated in mediating PCE's effects on female offspring neurobehavior.

