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ToxSci Advance Access originally published online on June 21, 2006
Toxicological Sciences 2006 93(1):125-135; doi:10.1093/toxsci/kfl046
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© The Author 2006. Published by Oxford University Press on behalf of the Society of Toxicology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

The Common Insecticides Cyfluthrin and Chlorpyrifos Alter the Expression of a Subset of Genes with Diverse Functions in Primary Human Astrocytes

Sarah M. Mense*, Amitabha Sengupta*, Changgui Lan*, Mei Zhou*, Galina Bentsman{dagger}, David J. Volsky{dagger}, Robin M. Whyatt*, Frederica P. Perera* and Li Zhang*,1

* Department of Environmental Health Sciences, Columbia University, Mailman School of Public Health, New York, New York 10032; and {dagger} Molecular Virology Division, St Luke's–Roosevelt Hospital Center and College of Physicians and Surgeons, Columbia University, New York, New York 10019

Received April 14, 2006; accepted June 2, 2006

Given the widespread use of insecticides in the environment, it is important to perform studies evaluating their potential effects on humans. Organophosphate insecticides, such as chlorpyrifos, are being phased out; however, the use of pyrethroids in household pest control is increasing. While chlorpyrifos is relatively well studied, much less is known about the potential neurotoxicity of cyfluthrin and other pyrethroids. To gain insights into the neurotoxicity of cyfluthrin, we compared and evaluated the toxicity profiles of chlorpyrifos and cyfluthrin in primary human fetal astrocytes. We found that at the same concentrations, cyfluthrin exerts as great as, or greater toxic effects on the growth, survival, and proper functioning of human astrocytes. By using microarray gene expression profiling, we systematically identified and compared the potential molecular targets of chlorpyrifos and cyfluthrin, at a genome-wide scale. We found that chlorpyrifos and cyfluthrin affect a similar number of transcripts. These targets include molecular chaperones, signal transducers, transcriptional regulators, transporters, and those involved in behavior and development. Further computational and biochemical analyses show that cyfluthrin and chlorpyrifos upregulate certain targets of the interferon-{gamma} and insulin-signaling pathways and that they increase the protein levels of activated extracellular signal–regulated kinase 1/2, a key component of insulin signaling; interleukin 6, a key inflammatory mediator; and glial fibrillary acidic protein, a marker of inflammatory astrocyte activation. These results suggest that inflammatory activation of astrocytes might be an important mechanism underlying neurotoxicity of both chlorpyrifos and cyfluthrin.

Key Words: chlorpyrifos; cyfluthrin; neurotoxicity; human astrocytes; inflammatory; microarray expression analysis.


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