Nicotine and the adolescent brain: insights from an animal model
Abstract
Tobacco use in adolescence represents one of the major challenges to the future of public health. Whereas numerous studies have explored the consequences of fetal or adult nicotine effects, little or no basic research has been conducted for nicotine during adolescence, the stage at which regular cigarette use typically begins. This review describes the recent development of a model of adolescent nicotine administration in rats that recapitulates the plasma levels of nicotine found in smokers. Adolescent nicotine evoked CNS nicotinic receptor up-regulation with a distinctly different regional pattern from that seen in the adult; increased receptor expression in male rats persisted for more than a month after discontinuing nicotine administration. We also identified evidence of cell damage and changes in cell size in the female hippocampus. These changes were accompanied by alterations in synaptic activity of cholinergic, noradrenergic, dopaminergic and serotonergic systems during nicotine administration and persisting for extended periods after the termination of exposure; behavioral alterations were commensurate with the neurochemical changes. In each case, the effects of adolescent nicotine differed not only from the adult, but also from the those seen after fetal exposure, indicating that adolescence represents a unique period of vulnerability for nicotine-induced misprogramming of brain cell development and synaptic function. Effects of nicotine on critical components of reward pathways and circuits involved in learning, memory and mood are likely to contribute to increased addictive properties and long-term behavioral problems seen in adolescent smokers.
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Laboratory animals also show a difference in nicotine sensitivity between adolescents and adults.
“The difference in sensitivity to nicotine between adolescents and adults is also reported for laboratory animals (Slotkin 2002; Adriani et al. 2003).”
From Short- and Long-Term Consequences of Nicotine Exposure during Adolescence for Prefrontal Cortex Neuronal Network Function (2012) · cites this paper as Slotkin 2002
The ability of nicotine to regulate β2*-nAChR availability may be age or sex dependent, because the nonhuman primates were male adolescents and the smokers were male and female adults.
“Although a species difference cannot be ruled out, this divergence may suggest that the ability of nicotine to regulate  2 *-nAChR availability is age or sex dependent because the nonhuman primates were male adolescents and the smokers were male and female adults (Slotkin, 2002;Nguyen et al., 2003).”
From Human Tobacco Smokers in Early Abstinence Have Higher Levels of β<sub>2</sub>* Nicotinic Acetylcholine Receptors than Nonsmokers (2006) · cites this paper as Slotkin, 2002
Prenatal nicotine exposure in rats at plasma levels comparable to human active smokers causes apoptosis, fewer neuronal cells, truncated axonogenesis, and deficient synaptogenesis.
“In developing rats exposed prenatally to nicotine at plasma levels comparable to those in human active smokers, standard biomarkers of cell injury indicate apoptosis, reductions in the numbers of neuronal cells, truncation of axonogenesis, and deficient synaptogenesis.”
From Developmental toxicity of nicotine: A transdisciplinary synthesis and implications for emerging tobacco products (2017) · cites this paper as [58]
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References 165 · Cited by 284
- Authors
- Slotkin, T.
- Affiliations
- Duke University (US)
- Corresponding author
- Slotkin, T
- ORCID
- Slotkin, T
- Venue
- Neurotoxicology and Teratology
- Publisher
- Elsevier BV
- Published
- 2002-06
- Volume
- 24
- Issue
- 3
- Pages
- 369-384
- ISSN
- 0892-0362 (ISSN-L)
- OpenAlex
- W2045971161
- Cited by
- 284
- References
- 165
- Citations by year
- 2026: 2 · 2025: 4 · 2024: 3 · 2023: 2 · 2022: 8 · 2021: 10 · 2020: 6 · 2019: 10 · 2018: 11 · 2017: 5 · 2016: 10 · 2015: 18 · 2014: 17 · 2013: 17 · 2012: 10
- FWCI
- 5.41
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neurotoxicology and Teratology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (5r01da014247-03)
- U.S. Public Health Service
- National Institute on Drug Abuse (DA14247)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nicotinic Acetylcholine Receptors Study
- Health Sciences › Medicine › Physiology › Smoking Behavior and Cessation
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Prenatal Substance Exposure Effects
- Keywords
- adolescent nicotine exposure, adolescent tobacco use, hippocampus, synaptic function, cholinergic system, noradrenergic system, dopaminergic system, serotonergic system, brain development, nicotine dependence, sex differences, brain vulnerability, reward pathways, learning and memory, mood
- MeSH terms
- Adolescent, Animals, Behavior, Animal, Brain, Female, Humans, Male, Nicotine, Receptors, Nicotinic, Smoking, Rats
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