The nematode Caenorhabditis elegans as a model of organophosphate-induced mammalian neurotoxicity.

Toxicol Appl Pharmacol

Department of Environmental Health Science, The University of Georgia, Athens, GA 30602-2102, USA.

Published: February 2004

AI Article Synopsis

  • The study tested 15 organic phosphate pesticides for their toxic effects on the nematode Caenorhabditis elegans, finding a significant correlation between the toxicity levels in C. elegans and traditional mammalian models (rats and mice).
  • Five of the eight chemicals tested showed strong cholinesterase inhibition, indicating a link between behavioral toxicity and biochemical activity.
  • The findings suggest that C. elegans can be a valuable model for assessing chemical toxicity and may enhance early screening processes for potential neurotoxins.

Article Abstract

Fifteen organic phosphate pesticides were tested by computer tracking for their acute behavioral toxicity with the nematode Caenorhabditis elegans. Thirteen of these 15 chemicals are used as insecticides and are anticholesterase agents. The other two chemicals are used as herbicides. EC50 values for each chemical were compared to the corresponding LD50 acute lethality value in rats and mice. Order of toxicity was found to be significantly correlated in comparisons of C. elegans to both rats and mice. Mechanistic investigations were conducted by assaying 8 of the 15 chemicals for anticholinesterase activity in C. elegans. Significant cholinesterase inhibition was confirmed for five chemicals that had displayed high behavioral toxicity, while three chemicals of low behavioral toxicity showed no significant decrease in cholinesterase activity. Toxicity for two chemicals that do not inhibit cholinesterase in mammals was linked to pH effects. Detailed comparison of individual chemicals and metabolic issues are discussed. These results have positive implications for the use of C. elegans as a mammalian neurological model and support the use of C. elegans in early rounds of chemical toxicity screening.

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Source
http://dx.doi.org/10.1016/j.taap.2003.09.013DOI Listing

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