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Long-term immunotoxic effects of combined prenatal and neonatal atrazine exposure in BALB/C mice

Public Domain


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  • Personal Author:
  • Description:
    Atrazine & its metabolites are present at high levels in a high percentage of water supplies in agro-intensive areas. Given that humans in these areas use water from these contaminated sources, we investigated the long-term effects of prenatal & neonatal exposure to atrazine on the immune system. To determine these effects, pregnant Balb/C dams were exposed to 700 g atrazine per day from day 10 postcoitus to day 10 postpartum. All offspring were allowed to nurse their natural mother & were weaned at 25 days of age. Offspring were randomly segregated by sex & exposure & aged to approximately 1 year of age at which time their spleens were removed for analysis. Phenotypic analysis was performed using flow cytometry & cytokine production was measured by cytometric bead array after anti- CD3/anti-CD28 stimulation of the spleen cells. The spleen cells were stained to determine total T cells, CD8+ T cells, CD4+ T cells, B cells, granulocytes, macrophages, NK cells, nTreg & LAG-3+-Treg cells. Cytokines measured include interleukin (IL)-2, IL-4, IL-6, interferon- , tumor necrosis factor- , IL-17A, IL-10 & TGF- 1 which measures the functional ability of the cells to respond to stimulation as well as allows for further classification of the T cells into TH1, TH2, TH17 cells. One year old female offspring had significant decreases in the percentage of CD8+ T cells & significant increases in granulocytes & NK cells. There was a trend (same type of change; 1 of 2 runs significant) towards an increase in LAG-3+ Treg cells. Male offspring showed significant decreases in the percentage of CD8+ T cells & significant increases in CD4+ as well as a trend towards a significant increase in NK cells. This is the first time the long term changes in immune cell phenotype have been documented after a prenatal & neonatal exposure to atrazine & it demonstrates that these early life exposures can result in permanent changes to the immune system. [Description provided by NIOSH]
  • Subjects:
  • Keywords:
  • ISSN:
    1096-6080
  • Document Type:
  • Genre:
  • Place as Subject:
  • CIO:
  • Division:
  • Topic:
  • Location:
  • Volume:
    120
  • NIOSHTIC Number:
    nn:20040265
  • Citation:
    Toxicologist 2011 Mar; 120(Suppl 2):143
  • CAS Registry Number:
  • Federal Fiscal Year:
    2011
  • Peer Reviewed:
    False
  • Source Full Name:
    The Toxicologist. Society of Toxicology 50th Annual Meeting and ToxExpo, March 6-10, 2011, Washington, DC
  • Supplement:
    2
  • Collection(s):
  • Main Document Checksum:
    urn:sha-512:091c8829ba88b1e5ecb71a77c8a382591929921d629b8780f59c21c2299268c9befecbc6f7ff38d8810921097f62a755437b22cc3445e2a80351e13fc7b2b9c2
  • Download URL:
  • File Type:
    Filetype[PDF - 59.04 KB ]
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