Does Prenatal Nicotine Exposure Sensitize the Brain to Nicotine-Induced Neurotoxicity in Adolescence?

• Published in: Neuropsychopharmacology (New York, N.Y.) Vol. 29; no. 8; pp. 1440 - 1450
• Main Authors: ABREU-VILLACA, Yael, SEIDLER, Frederic J, SLOTKIN, Theodore A
• Format: Journal Article
• Language: English
• Published: New York, NY Nature Publishing 01.08.2004; Nature Publishing Group
• Subjects: Aging - physiology; Animals; Biological and medical sciences; Body Weight - drug effects; Brain; Brain - drug effects; Brain - physiopathology; Cell Size; Child development; DNA - metabolism; Drug abuse; Female; Male; Medical sciences; Membrane Proteins - metabolism; Mesencephalon - drug effects; Mesencephalon - metabolism; Nerve Tissue Proteins - metabolism; Neurites - drug effects; Neurites - pathology; Neuroglia - drug effects; Neuroglia - pathology; Neurons - drug effects; Neurons - pathology; Neurotoxicity; Neurotoxicity Syndromes - physiopathology; Nicotine; Nicotine - administration & dosage; Nicotine - toxicity; Organ Size - drug effects; Pregnancy; Prenatal Exposure Delayed Effects; Proteins; Rats; Rats, Sprague-Dawley; Smoking; Tobacco, tobacco smoking; Toxicology; United States > US; Human; brain development; Cerebral cortex; Rat; Toxicity; Rodentia; Tobacco smoking; Midbrain; Encephalon; Pregnancy; Progeny; Alkaloid; Vertebrata; Neurotoxicity; Mammalia; cell damage; Animal; DNA; Adolescent; Development; adolescence; Lesion; Hippocampus; Nicotine
• ISSN: 0893-133X; 1740-634X
• DOI: 10.1038/sj.npp.1300443

Offspring of women who smoke during pregnancy are themselves more likely to take up smoking in adolescence. We evaluated neurotoxicant effects of prenatal and adolescent nicotine exposure in developing rats to evaluate whether these contribute to a biological basis for this relationship. Rats were given nicotine or vehicle throughout pregnancy and the offspring then again received nicotine or vehicle during adolescence (postnatal days PN30-47.5); this regimen reproduces the plasma nicotine levels found in smokers. Indices of neural cell number (DNA concentration and content), cell size (protein/DNA ratio), and cell membrane surface area (membrane/total protein) were then evaluated in brain regions during adolescent nicotine administration (PN45) and up to 1 month post-treatment. By itself, prenatal nicotine administration produced cellular alterations that persisted into adolescence, characterized by net cell losses in the midbrain and to a lesser extent, in the cerebral cortex, with corresponding elevations in the membrane/total protein ratio. The hippocampus showed a unique response, with increased DNA content and regional enlargement. Adolescent nicotine treatment alone had similar, albeit smaller effects, but also showed sex-dependence, with effects on protein biomarkers preferential to females. When animals exposed to nicotine prenatally were then given nicotine in adolescence, the net outcome was worsened, largely representing summation of the two individual effects. Our results indicate that prenatal nicotine exposure alters parameters of cell development lasting into adolescence, where the effects add to those elicited directly by adolescent nicotine; neurotoxicant actions may thus contribute to the association between maternal smoking and subsequent smoking in the offspring.