AI Article Synopsis

  • Developmental exposure to chlorpyrifos (CPF) in male mice showed a dose-dependent reduction in cholinesterase activity in both red blood cells and brain, particularly at higher CPF concentrations.
  • There was a significant decrease in doublecortin(+) cells in the subgranular zone and NeuN(+)-expressing mature neurons in the hilus at elevated CPF levels, indicating impaired neurogenesis during development.
  • The study suggests that while CPF exposure affects the maturation of granule cell lineages, these effects are transient and do not seem to alter overall hippocampal neurogenesis by postnatal day 77.

Article Abstract

The effect of developmental exposure to chlorpyrifos (CPF) on hippocampal neurogenesis was examined in male mice after maternal dietary exposure to CPF at 0, 4, 20, or 100ppm from gestation day 10 to postnatal day (PND) 21. Cholinesterase activity was dose-dependently decreased in red blood cells at ≥4ppm and in the brain at 100ppm both in dams and offspring on PND 21. Immunohistochemically, doublecortin(+) cells were decreased at ≥20ppm in the subgranular zone (SGZ) of the dentate gyrus, and NeuN(+)-expressing mature neurons were decreased at 100ppm in the hilus on PND 21. There were no differences in the numbers of progenitor populations expressing Tbr2 or M1 muscarinic acetylcholine receptors. Transcript levels of Dcx also decreased at ≥20ppm, and those of Pcna, Casp3, Bax, Bcl2, Pax6 and Tbr2 were unchanged in the dentate gyrus by real-time RT-PCR. At PND 77, hippocampal neurogenesis was unchanged. These results suggest that developmental CPF exposure directly but transiently suppresses maturation of late-stage granule cell lineages in the SGZ and affects interneuron populations in the hilus.

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http://dx.doi.org/10.1016/j.reprotox.2013.02.004DOI Listing

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