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. 2018 Jun 7;20(7):897-902.
doi: 10.1093/ntr/ntx177.

Prenatal Nicotine Exposure Disrupts Infant Neural Markers of Orienting

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Prenatal Nicotine Exposure Disrupts Infant Neural Markers of Orienting

Erin King et al. Nicotine Tob Res. .
Free PMC article


Introduction: Prenatal nicotine exposure (PNE) from maternal cigarette smoking is linked to developmental deficits, including impaired auditory processing, language, generalized intelligence, attention, and sleep. Fetal brain undergoes massive growth, organization, and connectivity during gestation, making it particularly vulnerable to neurotoxic insult. Nicotine binds to nicotinic acetylcholine receptors, which are extensively involved in growth, connectivity, and function of developing neural circuitry and neurotransmitter systems. Thus, PNE may have long-term impact on neurobehavioral development. The purpose of this study was to compare the auditory K-complex, an event-related potential reflective of auditory gating, sleep preservation and memory consolidation during sleep, in infants with and without PNE and to relate these neural correlates to neurobehavioral development.

Methods: We compared brain responses to an auditory paired-click paradigm in 3- to 5-month-old infants during Stage 2 sleep, when the K-complex is best observed. We measured component amplitude and delta activity during the K-complex.

Results: Infants with PNE demonstrated significantly smaller amplitude of the N550 component and reduced delta-band power within elicited K-complexes compared to nonexposed infants and also were less likely to orient with a head turn to a novel auditory stimulus (bell ring) when awake.

Conclusions: PNE may impair auditory sensory gating, which may contribute to disrupted sleep and to reduced auditory discrimination and learning, attention re-orienting, and/or arousal during wakefulness reported in other studies.

Implications: Links between PNE and reduced K-complex amplitude and delta power may represent altered cholinergic and GABAergic synaptic programming and possibly reflect early neural bases for PNE-linked disruptions in sleep quality and auditory processing. These may pose significant disadvantage for language acquisition, attention, and social interaction necessary for academic and social success.


Figure 1.
Figure 1.
(a) Difference in peak-to-peak amplitude between P200 and N550 components of K-complex by exposure group, adjusted for postmenstrual age at electroencephalogram (EEG). CTL = 17 drug-free infants, PNE = 16 with prenatal nicotine exposure. F = 3.74, p = .036. (b) Delta power of K-complex measured at the Cz electrode, adjusted for postmenstrual age at EEG, by group; F = 3.76, p = .035.

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