Skip Navigation
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Your Environment. Your Health.

Publication Detail

Title: Chlorpyrifos-, diisopropylphosphorofluoridate-, and parathion-induced behavioral and oxidative stress effects: are they mediated by analogous mechanisms of action?

Authors: López-Granero, Caridad; Cañadas, Fernando; Cardona, Diana; Yu, Yingchun; Giménez, Estela; Lozano, Rafael; Avila, Daiana Silva; Aschner, Michael; Sánchez-Santed, Fernando

Published In Toxicol Sci, (2013 Jan)

Abstract: Exposure to organophosphates (OPs) can lead to cognitive deficits and oxidative damage. Little is known about the relationship between behavioral deficits and oxidative stress within the context of such exposures. Accordingly, the first experiment was carried out to address this issue. Male Wistar rats were administered 250 mg/kg of chlorpyrifos (CPF), 1.5 mg/kg of diisopropylphosphorofluoridate (DFP), or 15 mg/kg of parathion (PTN). Spatial learning in the water maze task was evaluated, and F(2)-isoprostanes (F(2)-IsoPs) and prostaglandin (PGE(2)) were analyzed in the hippocampus. A second experiment was designed to determine the degree of inhibition of brain acetylcholinesterase (AChE) activity, both the soluble and particulate forms of the enzyme, and to assess changes in AChE gene expression given evidence on alternative splicing of the gene in response to OP exposures. In addition, brain acylpeptide hydrolase (APH) activity was evaluated as a second target for OP-mediated effects. In both experiments, rats were sacrificed at various points to determine the time course of OPs toxicity in relation to their mechanism of action. Results from the first experiment suggest cognitive and emotional deficits after OPs exposure, which could be due to, at least in part, increased F(2)-IsoPs levels. Results from the second experiment revealed inhibition of brain AChE and APH activity at various time points post OP exposure. In addition, we observed increased brain read-through splice variant AChE (AChE-R) mRNA levels after 48 h PTN exposure. In conclusion, this study provides novel data on the relationship between cognitive alterations and oxidative stress, and the diverse mechanisms of action along a temporal axis in response to OP exposures in the rat.

PubMed ID: 22986948 Exiting the NIEHS site

MeSH Terms: Acetylcholinesterase/genetics; Acetylcholinesterase/metabolism; Animals; Behavior, Animal/drug effects*; Chlorpyrifos/toxicity*; Dinoprostone/metabolism; F2-Isoprostanes/metabolism; Hippocampus/drug effects; Hippocampus/metabolism; Isoflurophate/toxicity*; Male; Maze Learning/drug effects; Oxidative Stress/drug effects*; Parathion/toxicity*; Peptide Hydrolases/metabolism; Rats; Rats, Wistar; Spatial Behavior/drug effects

Back
to Top