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ToxSci Advance Access published online on December 26, 2006

Toxicological Sciences, doi:10.1093/toxsci/kfl194
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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

Long-Lasting Reductions of Ethanol Drinking, Enhanced Ethanol-induced Sedation, and Decreased c-fos Expression in the Edinger-Westphal Nucleus in Wistar Rats Exposed to the Organophosphate Chlorpyrifos

F Carvajal*, M López-Grancha#, M Navarro§, MC Sánchez-Amate* and I Cubero*,1

* Departamento de Neurociencia y Ciencias de la Salud, University of Almería, Almería, Spain § Department of Psychology, University of North Carolina, Chapel Hill, USA # Department of Psychopharmacology, CNS Research Department, 31 av Paul Vaillant-Couturier, 92220 Bagneux, France

1 Corresponding author: Inmaculada Cubero, Ph.D., Assistant professor Email: icubero{at}ual.es Address: Department of Neurociencia y Ciencias de la Salud, University of Almería, 04120 Almería, Spain. Fax: 950-015473

Received October 18, 2006; accepted December 20, 2006


   Abstract

Intermittent or continuous exposure to a wide variety of chemically-unrelated environmental pollutants might result in the development of Multiple Chemical Intolerance (MCS) and increased sensitivity to drugs of abuse. Interestingly, clinical evidence suggests that exposure to organophosphates might be linked to increased ethanol sensitivity and reduced voluntary consumption of ethanol-containing beverages in humans. The growing body of clinical and experimental evidence emerging in this new scientific field that bridges environmental health sciences, toxicology, and drug research, calls for well controlled studies aimed to analyze the nature of the neurobiological interactions of drugs and pollutants. Present study specifically evaluated neurobiological and behavioral responses to ethanol in Wistar rats that were previously exposed to the pesticide Organophosphate Chlorpyrifos (CPF). In agreement with clinical data, animals pre-treated with a single injection of CPF showed long-lasting ethanol avoidance that was not secondary to altered gustatory processing or enhancement of the aversive properties of ethanol. Furthermore, CPF pre-treatment increased ethanol-induced sedation without altering blood ethanol levels. An immunocytochemical assay revealed reduced c-fos expression in the Edinger-Westphal nucleus following CPF treatment, a critical brain area that has been implicated in ethanol intake and sedation. We hypothesize that that CPF might modulate cellular mechanisms (decreased intracellular cAMP signalling, alpha-7-nicotinic receptors and/or cerebral AChE inhibition) in neuronal pathways critically involved in neurobiological responses to ethanol.

Key Words: Chlorpyrifos; Ethanol avoidance; Chemical intolerance; Edinger-Westphal nucleus; Cholinesterase inhibition; Organophosphates.


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