Elevated NMDA receptor levels and enhanced postsynaptic long-term potentiation induced by prenatal exposure to valproic acid

Tania Rinaldi, Karina Kulangara, Katia Antoniello, Henry Markram, Tania Rinaldi Barkat

    192 Citations (Scopus)

    Abstract

    Valproic acid (VPA) is a powerful teratogen causing birth defects in humans, including autism spectrum disorder (ASD), if exposure occurs during the first trimester of embryogenesis. Learning and memory alterations are common symptoms of ASD, but underlying molecular and synaptic alterations remain unknown. We therefore studied plasticity-related mechanisms in the neocortex of 2-week-old rats prenatally exposed to VPA and tested for changes in glutamate-mediated transmission and plasticity in the neocortex. We found a selective overexpression of NR2A and NR2B subunits of NMDA receptors, as well as the commonly linked kinase calcium/calmodulin-dependent protein kinase II. Synaptic plasticity experiments between pairs of pyramidal neurons revealed an augmented postsynaptic form of long-term potentiation. These results indicate that VPA significantly enhances NMDA receptor-mediated transmission and causes increased plasticity in the neocortex. Enhanced plasticity introduces a surprising perspective to the potential molecular and synaptic mechanisms involved in children prenatally exposed to VPA.
    Original languageEnglish
    JournalProceedings of the National Academy of Sciences of the United States of America
    Volume104
    Issue number33
    Pages (from-to)13501-6
    Number of pages6
    ISSN0027-8424
    DOIs
    Publication statusPublished - 14 Aug 2007

    Keywords

    • Action Potentials
    • Animals
    • Anticonvulsants
    • Calcium
    • Female
    • Long-Term Potentiation
    • Maternal Exposure
    • Pregnancy
    • Rats
    • Rats, Wistar
    • Receptors, N-Methyl-D-Aspartate
    • Synapses
    • Valproic Acid

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