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An Integrated Systems Approach to Decode the Impact of Adolescent Nicotine Exposure in Utero and Postnatally
Adrian Flores1, Austin Gowen1, Victoria L Schaal1
1University of Nebraska Medical Center (UNMC).
Insights
Opioid-exposed offspring show increased vulnerability to nicotine during adolescence. This study reveals neurodevelopmental and behavioral deficits following combined perinatal opioid and adolescent nicotine exposure.
Area of Science:
- Neuroscience
- Developmental Biology
- Toxicology
Background:
- Perinatal opioid exposure, specifically oxycodone, causes neurodevelopmental and behavioral deficits in offspring.
- The interaction between perinatal opioid exposure and adolescent nicotine use is understudied, despite nicotine's prevalence.
Approach:
- Investigated the effects of escalating adolescent nicotine exposure and withdrawal in offspring exposed to oxycodone either in utero (IUO) or postnatally (PNO).
- Utilized Western blot, RT-qPCR, and behavioral assays to assess blood-brain barrier integrity, synaptic proteins, neuroinflammation, nicotine metabolism, and withdrawal behaviors.
Key Points:
- Nicotine exposure altered blood-brain barrier and synaptic proteins in IUO and PNO offspring.
- Evidence of central nervous system immune dysfunction and compromised blood-brain barrier integrity was observed.
- Increased peripheral nicotine catabolism in exposed offspring suggests a higher risk for addiction.
Conclusions:
- Adolescent nicotine exposure and withdrawal exacerbate vulnerabilities in offspring prenatally exposed to opioids.
- This research highlights critical neurodevelopmental and behavioral consequences of combined exposures during sensitive developmental periods.
Abstract:
Perinatal exposure to prescription opioids pose a critical public health risk. Notably, research has found significant neurodevelopmental and behavioral deficits between in utero (IUO) and postnatal (PNO) oxycodone-exposed offspring but there is a notable gap in knowledge regarding the interaction of these groups to other drug exposure, particularly nicotine exposure. Nicotine's widespread use represents a ubiquitous clinical interaction that current research does not address. Children often experiment with drugs and risky behavior; therefore, adolescence is a key timepoint to characterize. This study employed an integrated systems approach to investigate escalating nicotine exposure in adolescence and subsequent nicotine withdrawal in the IUO- and PNO-offspring. Western blot analysis found alterations of the blood-brain barrier (B.B.B.) and synaptic proteins. RT-qPCR further validated immune dysfunction in the central nervous system (CNS) consistent with compromised B.B.B. Peripheral nicotine metabolism was consistent with increased catabolism of nicotine concerning PNO & IUO, a predictor of greater addiction risk. Lastly, behavioral assays found subtle deficits to withdrawal in nociception and anxiety-like behavior. This study showed, for the first time, the vulnerabilities of PNO- and IUO-exposed groups concerning nicotine use during early adolescence and withdrawal.
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