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Moderate Prenatal Alcohol Exposure and Quantification of Social Behavior in Adult Rats
Published on: December 14, 2014
Perigestational Opioid Exposure Alters Alcohol-Driven Reward Behaviors in Adolescent Rats
Christopher T Searles1, Hannah J Harder1, Meghan E Vogt1
1Neuroscience Institute, Georgia State University, 100 Piedmont Ave., Atlanta, GA, 30303.
Insights
Babies born with neonatal opioid withdrawal syndrome (NOWS) may face altered alcohol use later in life. Perigestational opioid exposure impacts reward-seeking behaviors and opioid receptor expression in rats.
Area of Science:
- Neuroscience
- Developmental Biology
- Addiction Research
Background:
- Neonatal opioid withdrawal syndrome (NOWS) rates have surged sevenfold since 2004.
- Intrauterine drug exposure is a known risk factor for adult health issues, including future substance use.
- Limited data exists on the long-term risks of alcohol use in individuals with NOWS.
Purpose of the Study:
- To investigate the impact of perigestational opioid exposure (POE) on the mesolimbic reward system in male and female rats.
- To assess how early-life opioid exposure affects alcohol consumption and reward-seeking behaviors during postnatal and adolescent development.
Main Methods:
- Utilized a clinically relevant rat model of morphine exposure from pre-conception to the first week of life.
- Measured alcohol consumption under noncontingent and operant conditioning paradigms.
- Analyzed μ-opioid receptor expression in key reward circuitry regions (nucleus accumbens, medial habenula).
Main Results:
- Perigestational opioid exposure (POE) increased alcohol consumption in female rats under noncontingent conditions.
- POE reduced alcohol consumption in both male and female rats during operant conditioning.
- Operant responding for sucrose was also reduced, indicating broader effects on reward-seeking.
- Significant alterations in μ-opioid receptor expression were observed in the nucleus accumbens and medial habenula.
Conclusions:
- Early-life opioid exposure can significantly alter alcohol consumption patterns and reward system function.
- The effects of POE on reward-seeking behaviors extend beyond drugs of abuse.
- Findings highlight potential long-term neurological consequences of NOWS relevant to future alcohol use risk.
Abstract:
Every fifteen minutes, a baby is born in the U.S. experiencing neonatal opioid withdrawal syndrome (NOWS). Since 2004, the rate of NOWS has increased 7-fold. Clinical studies have established intrauterine exposure to drugs of abuse as a risk factor for adverse health outcomes in adult life, including the propensity for future illicit drug use. Despite extensive knowledge about common mechanisms of action in the neural circuitry that drives opioid and alcohol reward, there is little data on the risks that those born with NOWS face regarding alcohol use later in life. Here, we investigate the impact of perigestational opioid exposure (POE) on the mesolimbic reward system of male and female Sprague Dawley rats at postnatal and adolescent ages. Our laboratory has developed a clinically relevant model for morphine exposure spanning pre-conception to the first week of life. Using this model, we found that POE increased alcohol consumption in female rats under noncontingent conditions, and inversely, reduced alcohol consumption in both male and female rats during operant conditioning sessions. Operant responding was also reduced for sucrose, suggesting that the impact of POE on reward-seeking behaviors is not limited to drugs of abuse. Expression of μ-opioid receptors was also significantly altered in the nucleus accumbens and medial habenula, regions previously shown to play a significant role in reward/aversion circuitry.
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