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Effects of prenatal nicotine exposure on primate brain development and attempted amelioration with supplemental choline or vitamin C: neurotransmitter receptors, cell signaling and cell development biomarkers in fetal brain regions of rhesus monkeys.

Publication ,  Journal Article
Slotkin, TA; Seidler, FJ; Qiao, D; Aldridge, JE; Tate, CA; Cousins, MM; Proskocil, BJ; Sekhon, HS; Clark, JA; Lupo, SL; Spindel, ER
Published in: Neuropsychopharmacology
January 2005

Studies in developing rodents indicate that nicotine is a neuroteratogen that disrupts brain development by stimulating nicotinic acetylcholine receptors (nAChRs) that control neural cell replication and differentiation. We administered nicotine to pregnant Rhesus monkeys from gestational day 30 through 160 by continuous infusion, achieving maternal plasma levels comparable to those in smokers (30 ng/ml). Fetal brain regions and peripheral tissues were examined for nAChR subtypes, other neurotransmitter receptors, and indices of cell signaling and cell damage. Nicotine evoked nAChR upregulation, but with distinct regional disparities indicative of selective stimulatory responses. Similarly, indices of cell loss (reduced DNA), cell size and neuritic outgrowth (protein/DNA and membrane/total protein ratios) were distinct for each region and did not necessarily follow the rank order of nAChR upregulation, suggesting the involvement of additional mechanisms such as oxidative stress. We then attempted to offset the adverse effects of nicotine with standard dietary supplements known to interact with nicotine. By itself, choline elicited nicotine-like actions commensurate with its promotion of cholinergic neurotransmission. When given in combination with nicotine, choline protected some regions from damage but worsened nicotine's effects in other regions. Similarly, Vitamin C supplementation had mixed effects, increasing nAChR responses while providing protection from cell damage in the caudate, the brain region most susceptible to oxidative stress. Our results indicate that nicotine elicits neurodevelopmental damage that is highly selective for different brain regions, and that dietary supplements ordinarily thought to be neuroprotectant may actually worsen some of the adverse effects of nicotine on the fetal brain.

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Published In

Neuropsychopharmacology

DOI

ISSN

0893-133X

Publication Date

January 2005

Volume

30

Issue

1

Start / End Page

129 / 144

Location

England

Related Subject Headings

  • Thiobarbituric Acid Reactive Substances
  • Signal Transduction
  • Receptors, Neurotransmitter
  • Psychiatry
  • Prenatal Exposure Delayed Effects
  • Pregnancy
  • Oxidative Stress
  • Nootropic Agents
  • Nicotinic Agonists
  • Nicotine
 

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Slotkin, T. A., Seidler, F. J., Qiao, D., Aldridge, J. E., Tate, C. A., Cousins, M. M., … Spindel, E. R. (2005). Effects of prenatal nicotine exposure on primate brain development and attempted amelioration with supplemental choline or vitamin C: neurotransmitter receptors, cell signaling and cell development biomarkers in fetal brain regions of rhesus monkeys. Neuropsychopharmacology, 30(1), 129–144. https://doi.org/10.1038/sj.npp.1300544
Slotkin, Theodore A., Frederic J. Seidler, Dan Qiao, Justin E. Aldridge, Charlotte A. Tate, Mandy M. Cousins, Becky J. Proskocil, et al. “Effects of prenatal nicotine exposure on primate brain development and attempted amelioration with supplemental choline or vitamin C: neurotransmitter receptors, cell signaling and cell development biomarkers in fetal brain regions of rhesus monkeys.Neuropsychopharmacology 30, no. 1 (January 2005): 129–44. https://doi.org/10.1038/sj.npp.1300544.
Slotkin TA, Seidler FJ, Qiao D, Aldridge JE, Tate CA, Cousins MM, Proskocil BJ, Sekhon HS, Clark JA, Lupo SL, Spindel ER. Effects of prenatal nicotine exposure on primate brain development and attempted amelioration with supplemental choline or vitamin C: neurotransmitter receptors, cell signaling and cell development biomarkers in fetal brain regions of rhesus monkeys. Neuropsychopharmacology. 2005 Jan;30(1):129–144.
Journal cover image

Published In

Neuropsychopharmacology

DOI

ISSN

0893-133X

Publication Date

January 2005

Volume

30

Issue

1

Start / End Page

129 / 144

Location

England

Related Subject Headings

  • Thiobarbituric Acid Reactive Substances
  • Signal Transduction
  • Receptors, Neurotransmitter
  • Psychiatry
  • Prenatal Exposure Delayed Effects
  • Pregnancy
  • Oxidative Stress
  • Nootropic Agents
  • Nicotinic Agonists
  • Nicotine