Literature DB >> 16783542

Paradoxical effects of prenatal acetylcholinesterase blockade on neuro-behavioral development and drug-induced stereotypies in reeler mutant mice.

Giovanni Laviola1, Walter Adriani, Chiara Gaudino, Ramona Marino, Flavio Keller.   

Abstract

INTRODUCTION: Epidemiological and experimental studies support a link between genetic and epigenetic factors in vulnerability to develop enduring neurobehavioral alterations. We studied the interplay between genetic vulnerability and the prenatal exposure to a neurotoxic compound. Chlorpyrifos, a potent and reversible acetylcholinesterase blocker used as a pesticide, and the "reeler" mouse, lacking the extracellular-matrix protein Reelin, were used.
MATERIALS AND METHODS: Homozygous reeler (RL), heterozygous (HZ), and wild-type (WT) mice were prenatally exposed to chlorpyrifos-oxon (CPF-O), the active metabolite of chlorpyrifos, or to vehicle (prenatal controls) on gestation days 14-16, that is, during a peak period of neurogenesis in the cerebral cortex. The offspring was reared by the natural dam and tested during infancy and at adulthood for global consequences of the prenatal exposure.
CONCLUSION: The results are consistent with complex interactions between genetic (reeler genotype) and epigenetic (prenatal exposure to CPF-O) factors. In the case of some "genetically modulated" parameters (ultrasound vocalization, amphetamine-induced locomotion, and stereotypy), exposure to CPF-O paradoxically reverted the effects produced by progressive reelin absence. Conversely, for an "epigenetically modulated" parameter (grasping reflex maturation), the effects of CPF-O exposure were counteracted by progressive reelin absence. Finally, for parameters apparently untouched by either factor alone (righting reflex latency, scopolamine-induced locomotor activity), prenatal CPF-O exposure unmasked an otherwise latent genotype dependency. This complex picture also points to reciprocal adaptations within cholinergic and dopaminergic systems during development. Data are interesting in view of recently discovered cholinergic abnormalities in autism and schizophrenia, and may suggest new avenues for early intervention.

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Year:  2006        PMID: 16783542     DOI: 10.1007/s00213-006-0426-z

Source DB:  PubMed          Journal:  Psychopharmacology (Berl)        ISSN: 0033-3158            Impact factor:   4.530


  58 in total

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4.  Muscarinic cholinergic hyperactivity in schizophrenia. Relationship to positive and negative symptoms.

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5.  Reelin in the extracellular matrix and dendritic spines of the cortex and hippocampus: a comparison between wild type and heterozygous reeler mice by immunoelectron microscopy.

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8.  Nicotinic receptor abnormalities in the cerebellar cortex in autism.

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9.  Acetylcholinesterase level and molecular isoforms are altered in brain of Reelin Orleans mutant mice.

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10.  Alterations in central nervous system serotonergic and dopaminergic synaptic activity in adulthood after prenatal or neonatal chlorpyrifos exposure.

Authors:  Justin E Aldridge; Armando Meyer; Frederic J Seidler; Theodore A Slotkin
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  31 in total

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Authors:  Abby A Li; Kimberly A Lowe; Laura J McIntosh; Pamela J Mink
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2.  Animal models of gene-environment interactions in schizophrenia.

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Review 5.  Animal models of gene-environment interaction in schizophrenia: A dimensional perspective.

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6.  Nicotine exposure during adolescence: cognitive performance and brain gene expression in adult heterozygous reeler mice.

Authors:  Emilia Romano; Federica De Angelis; Lisa Ulbrich; Antonella De Jaco; Andrea Fuso; Giovanni Laviola
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7.  Nicotine restores Wt-like levels of reelin and GAD67 gene expression in brain of heterozygous reeler mice.

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8.  Impulsivity as long-term sequelae after chlorpyrifos intoxication: time course and individual differences.

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10.  Persistent cognitive alterations in rats after early postnatal exposure to low doses of the organophosphate pesticide, diazinon.

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