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Persistent cholinergic presynaptic deficits after neonatal chlorpyrifos exposure.

Publication ,  Journal Article
Slotkin, TA; Cousins, MM; Tate, CA; Seidler, FJ
Published in: Brain Res
June 1, 2001

The commonly-used organophosphate insecticide, chlorpyrifos (CPF), impairs brain cell development, axonogenesis and synaptogenesis. In the current study, we administered CPF to neonatal rats on postnatal (PN) days 1-4 (1 mg/kg) or PN11-14 (5 mg/kg), treatments that were devoid of overt toxicity. We then examined two cholinergic synaptic markers, choline acetyltransferase activity (ChAT) and [3H]hemicholinium-3 binding (HC-3) in the hippocampus, midbrain, striatum, brainstem and cerebral cortex in the juvenile (PN30) and young adult (PN60). Across all brain regions, CPF exposure evoked significant reductions in both markers, with larger effects on HC-3 binding, which is responsive to neuronal impulse activity, than on ChAT, a constitutive marker. Superimposed on the deficits, there were gender-selective effects and distinct regional disparities in the critical exposure period for vulnerability. In the hippocampus, either the early or late treatment regimen evoked decreases in ChAT but the early regimen elicited a much larger decrease in HC-3; effects persisted into adulthood. In the midbrain, CPF administration on PN1-4 elicited deficits similar to those seen in the hippocampus; however, exposure on PN11-14 elicited changes preferentially in females. Gender selectivity was also apparent in the striatum, in this case reflecting deficits in females after CPF treatment on PN1-4. In contrast, the effects of CPF on the brainstem were relatively more robust in males; effects in the cerebral cortex were less notable than in other regions. These results indicate that neonatal CPF exposure produces widespread deficiencies in cholinergic synaptic function that persist into adulthood. The effects are likely to contribute to gender-selective alterations in behavioral performance that persist or emerge long after the termination of exposure and well after the restoration of cholinesterase activity.

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Published In

Brain Res

DOI

ISSN

0006-8993

Publication Date

June 1, 2001

Volume

902

Issue

2

Start / End Page

229 / 243

Location

Netherlands

Related Subject Headings

  • Tritium
  • Symporters
  • Sex Factors
  • Rats, Sprague-Dawley
  • Rats
  • Presynaptic Terminals
  • Plasma Membrane Neurotransmitter Transport Proteins
  • Neurology & Neurosurgery
  • Nerve Tissue Proteins
  • Neostriatum
 

Citation

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Slotkin, T. A., Cousins, M. M., Tate, C. A., & Seidler, F. J. (2001). Persistent cholinergic presynaptic deficits after neonatal chlorpyrifos exposure. Brain Res, 902(2), 229–243. https://doi.org/10.1016/s0006-8993(01)02387-3
Slotkin, T. A., M. M. Cousins, C. A. Tate, and F. J. Seidler. “Persistent cholinergic presynaptic deficits after neonatal chlorpyrifos exposure.Brain Res 902, no. 2 (June 1, 2001): 229–43. https://doi.org/10.1016/s0006-8993(01)02387-3.
Slotkin TA, Cousins MM, Tate CA, Seidler FJ. Persistent cholinergic presynaptic deficits after neonatal chlorpyrifos exposure. Brain Res. 2001 Jun 1;902(2):229–43.
Slotkin, T. A., et al. “Persistent cholinergic presynaptic deficits after neonatal chlorpyrifos exposure.Brain Res, vol. 902, no. 2, June 2001, pp. 229–43. Pubmed, doi:10.1016/s0006-8993(01)02387-3.
Slotkin TA, Cousins MM, Tate CA, Seidler FJ. Persistent cholinergic presynaptic deficits after neonatal chlorpyrifos exposure. Brain Res. 2001 Jun 1;902(2):229–243.
Journal cover image

Published In

Brain Res

DOI

ISSN

0006-8993

Publication Date

June 1, 2001

Volume

902

Issue

2

Start / End Page

229 / 243

Location

Netherlands

Related Subject Headings

  • Tritium
  • Symporters
  • Sex Factors
  • Rats, Sprague-Dawley
  • Rats
  • Presynaptic Terminals
  • Plasma Membrane Neurotransmitter Transport Proteins
  • Neurology & Neurosurgery
  • Nerve Tissue Proteins
  • Neostriatum