Reference : Anxiety in adult female mice following perinatal exposure to chlorpyrifos.
Scientific journals : Article
Life sciences : Environmental sciences & ecology
http://hdl.handle.net/2268/21499
Anxiety in adult female mice following perinatal exposure to chlorpyrifos.
English
Braquenier, Jean-Baptiste[Université de Liège - ULG > Département des sciences et gestion de l'environnement > Ecophysiologie et physiologie animale > >]
Quertemont, Etienne[Université de Liège - ULg > Département des sciences cognitives > Psychologie quantitative >]
Tirelli, Ezio[Université de Liège - ULg > Département des sciences cognitives > Neuroscience comportementale et psychopharmacologie expér. >]
Plumier, Jean-Christophe[Université de Liège - ULg > Département des sciences et gestion de l'environnement > Ecophysiologie et physiologie animale >]
[en] Epidemiologic studies suggested a possible link between prenatal exposure to organophosphate insecticides (OP) and long-term mental delay and some behavioral troubles. Experimental studies in rats and mice have confirmed that a relatively short exposure to low doses of OP such as chlorpyrifos (CPF) during specific perinatal periods decreased anxiety-like behaviors. In the present study, we report that chronic perinatal exposure (GD15-PND14) to low doses of CPF leads to an increase (and not a decrease) in anxiety-like behaviors of female mouse offspring. Pregnant or lactating female mice were exposed to CPF (0.2; 1; or 5 mg/kg day) by oral treatment during 18 consecutive days. Following a recovery period of several weeks, the anxiety of adult female offspring was determined using neurobehavioral tests (elevated plus-maze and light/dark box tests). Our results showed that CPF-exposed female offspring were more anxious than controls. In addition, the magnitude of anxiety profile alterations depended on the level of exposure to CPF during gestation and lactation with a maximal effect observed at the 1 mg/kg day dose. Our results confirm that OP exposure during the perinatal period can induce long-term alterations in mouse anxiety-like behaviors and suggest that the routes of administration and the duration of OP exposure during brain development may be factors to consider when studying the development of anxiety.