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National Institute of Environmental Health Sciences

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Publication Detail

Title: Effect of organophosphorus insecticides and their metabolites on astroglial cell proliferation.

Authors: Guizzetti, Marina; Pathak, Shantha; Giordano, Gennaro; Costa, Lucio G

Published In Toxicology, (2005 Nov 15)

Abstract: Though little attention has been given to the possibility that glial cells may represent a target for the developmental neurotoxicity of organophosphorus (OP) insecticides, recent evidence, obtained in particular with chlorpyrifos (CP), suggests that developmental exposure to this compound may indeed target astrocytes. To substantiate and expand these observations, we carried out a series of in vitro studies utilizing fetal rat astrocytes and a human astrocytoma cell line, 1321N1 cells, to investigate the effect of the OPs CP, diazinon (DZ) and parathion (P), their oxygen analogs chlorpyrifos oxon (CPO), diazoxon (DZO) and paraoxon (PO), and their metabolites 3,5,6-trichloro-2-pyridinol (TCP), 2-isopropyl-6-methyl-4-pyrimidol (IMP) and para-nitrophenol (PNP), on cell proliferation. In fetal rat astrocytes and astrocytoma cells maintained in serum, CP, DZ, P, CPO, DZO, and PO induced a concentration-dependent inhibition in [(3)H]thymidine incorporation with a very similar potency (IC(50) between 45 and 57 microM). Among the other metabolites, PNP was the most potent (IC(50)=70-80 microM), while TCP and IMP were much less effective (IC(50)>100 microM). Cytotoxicity appears to account only for a small part of the effect on DNA synthesis. OP insecticides and their oxons were three- to six-fold more potent in inhibiting [(3)H]thymidine incorporation when cells were synchronized in the G(0)/G(1) phase of the cell cycle and re-stimulated by carbachol or epidermal growth factor. These results suggest that OP insecticides and their oxons affect astroglial cell proliferation and that the transition from the G(0)/G(1) to the S/G(2) phase of the cell cycle may be particularly sensitive to the action of these compounds.

PubMed ID: 16102884 Exiting the NIEHS site

MeSH Terms: No MeSH terms associated with this publication

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