Ontogenetic alterations in molecular and structural correlates of dendritic growth after developmental exposure to polychlorinated biphenyls

Environ Health Perspect. 2007 Apr;115(4):556-63. doi: 10.1289/ehp.9773. Epub 2007 Jan 16.

Abstract

Objective: Perinatal exposure to polychlorinated biphenyls (PCBs) is associated with decreased IQ scores, impaired learning and memory, psychomotor difficulties, and attentional deficits in children. It is postulated that these neuropsychological deficits reflect altered patterns of neuronal connectivity. To test this hypothesis, we examined the effects of developmental PCB exposure on dendritic growth.

Methods: Rat dams were gavaged from gestational day 6 through postnatal day (PND) 21 with vehicle (corn oil) or the commercial PCB mixture Aroclor 1254 (6 mg/kg/day). Dendritic growth and molecular markers were examined in pups during development.

Results: Golgi analyses of CA1 hippocampal pyramidal neurons and cerebellar Purkinje cells indicated that developmental exposure to PCBs caused a pronounced age-related increase in dendritic growth. Thus, even though dendritic lengths were significantly attenuated in PCB-treated animals at PND22, the rate of growth was accelerated at later ages such that by PND60, dendritic growth was comparable to or even exceeded that observed in vehicle controls. Quantitative reverse transcriptase polymerase chain reaction analyses demonstrated that from PND4 through PND21, PCBs generally increased expression of both spinophilin and RC3/neurogranin mRNA in the hippocampus, cerebellum, and cortex with the most significant increases observed in the cortex.

Conclusions: This study demonstrates that developmental PCB exposure alters the ontogenetic profile of dendritogenesis in critical brain regions, supporting the hypothesis that disruption of neuronal connectivity contributes to neuropsychological deficits seen in exposed children.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, N.I.H., Intramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Cell Enlargement
  • Child
  • Cognition Disorders / chemically induced
  • Dendritic Cells / drug effects*
  • Developmental Disabilities / chemically induced
  • Disease Models, Animal
  • Environmental Pollutants / toxicity*
  • Female
  • Humans
  • Polychlorinated Biphenyls / toxicity*
  • Pregnancy
  • Prenatal Exposure Delayed Effects*
  • Purkinje Cells / drug effects
  • Pyramidal Tracts / cytology
  • Pyramidal Tracts / drug effects
  • Rats
  • Rats, Long-Evans

Substances

  • Environmental Pollutants
  • Polychlorinated Biphenyls