Neurological impairment in fetal mouse brain by drinking water disinfectant byproducts

Ahmed E. Ahmed, Gerald Campbell, Sam Jacob

Research output: Contribution to journalArticle

19 Citations (Scopus)

Abstract

Developmental exposure to environmental chemicals may have detrimental effects on embryonic brains that could play a major role in the etio-pathology of fetal and adult neurological diseases. The exact mechanism by which prenatal exposures to environmental agents, such as drinking water disinfectant byproducts (DBP), cause neurological impairment in fetus is not known. Our objective is to examine the impact of prenatal exposure to DBP on fetal brain development. Pregnant CD-1 mice, at the sixth day of gestation (GD-6), received a daily (GD-6-GD-18) oral dose of chloroacetonitrile (CAN, 25 ppm), a member of DBP. To assess fetal brain uptake of CAN, several animals were injected with a tracer dose of 2-[14C]-CAN (333 μCi/kg, i.v.), at GD-12 and processed for quantitative in situ micro whole-body autoradiography (QIMWBA) at 1 and 24 h after treatment. The remaining animals continued receiving CAN until GD-18 when fetal brains were processed for biochemical determination of oxidative stress (OS) or prepared for histological examinations. The results indicate a rapid placental transfer and fetal brain uptake of 2-[ 14C]-CAN/metabolites in cortical areas and hippocampus. In treated animals 3-fold decrease in glutathione (GSH), 1.3-fold increase in lipid peroxidation and 1.4-fold increase in DNA oxidation were detected as compared to control. DeOlmos cupric silver staining of fetal brains indicated significant increase in cortical neurodegeneration in treated animals. Immunohistochemical labeling (TUNEL) of apoptotic nuclei in the cortices and choroid plexuses were also increased in treated animals as compared to control. In conclusion, CAN crosses the placental and fetal blood-brain barriers and induces OS that triggered apoptotic neurodegenration in fetal brain. Future studies will examine the molecular mechanisms of these events and its impact on neural development of offspring.

Original languageEnglish (US)
Pages (from-to)633-640
Number of pages8
JournalNeuroToxicology
Volume26
Issue number4 SPEC. ISS.
DOIs
StatePublished - Aug 2005

Fingerprint

Disinfectants
Drinking Water
Byproducts
Brain
Animals
Oxidative stress
Environmental Exposure
Oxidative Stress
Silver Staining
Choroid Plexus
In Situ Nick-End Labeling
Pathology
Metabolites
Fetal Development
Blood-Brain Barrier
Autoradiography
Fetal Blood
Silver
Labeling
Lipid Peroxidation

Keywords

  • Chloroacetonitrile
  • Fetal brain development
  • Haloacetonitriles
  • Oxidative stress
  • Water disinfection byproducts
  • Whole body autoradiography

ASJC Scopus subject areas

  • Cellular and Molecular Neuroscience
  • Neuroscience(all)
  • Toxicology

Cite this

Neurological impairment in fetal mouse brain by drinking water disinfectant byproducts. / Ahmed, Ahmed E.; Campbell, Gerald; Jacob, Sam.

In: NeuroToxicology, Vol. 26, No. 4 SPEC. ISS., 08.2005, p. 633-640.

Research output: Contribution to journalArticle

Ahmed, Ahmed E. ; Campbell, Gerald ; Jacob, Sam. / Neurological impairment in fetal mouse brain by drinking water disinfectant byproducts. In: NeuroToxicology. 2005 ; Vol. 26, No. 4 SPEC. ISS. pp. 633-640.
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