Abstract

Valproic acid (VPA) is widely prescribed to treat epilepsy. Maternal VPA use is, however, clinically restricted because of the severe risk that VPA may cause neurodevelopmental disorders in offspring, such as autism spectrum disorder. Understanding the negative action of VPA may help to prevent VPA-induced neurodevelopmental disorders. Astrocytes play a vital role in neurodevelopment and synapse function; however, the impact of VPA on astrocyte involvement in neurodevelopment and synapse function has not been examined. In this study, we examined whether exposure of cultured astrocytes to VPA alters neuronal morphology and synapse function of co-cultured neurons. We show that synaptic transmission by inhibitory neurons was small because VPA-exposed astrocytes reduced the number of inhibitory synapses. However, synaptic transmission by excitatory neurons and the number of excitatory synapses were normal with VPA-exposed astrocytes. VPA-exposed astrocytes did not affect the morphology of inhibitory neurons. These data indicate that VPA-exposed astrocytes impair synaptogenesis specifically of inhibitory neurons. Our results indicate that maternal use of VPA would affect not only neurons but also astrocytes and would result in perturbed astrocyte-mediated neurodevelopment.

Highlights

  • Valproic acid (VPA) is widely prescribed to treat epilepsy

  • Patch clamps were performed on mass culture preparations and compared among four groups of astrocytes exposed to different concentrations of VPA (0 mM, 0.3 mM, 1 mM and 3 mM)

  • We investigated whether VPA-exposed astrocytes affect synaptic properties of co-cultured neurons

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Summary

Introduction

Valproic acid (VPA) is widely prescribed to treat epilepsy. Maternal VPA use is, clinically restricted because of the severe risk that VPA may cause neurodevelopmental disorders in offspring, such as autism spectrum disorder. We show that synaptic transmission by inhibitory neurons was small because VPA-exposed astrocytes reduced the number of inhibitory synapses. Synaptic transmission by excitatory neurons and the number of excitatory synapses were normal with VPA-exposed astrocytes. VPA exposure of cultured cortical neurons derived from postnatal day 1 rats suppresses the formation of GABAergic synapses, but not glutamatergic ­synapses[12]. It is clear that VPA exposure has an effect on neuronal development It is unknown whether VPA exposure of astrocytes, which play important roles in synapse formation and in modulation of synaptic function, has an effect on neurodevelopment. We found changes to the synaptic function of cortical inhibitory, but not excitatory, neurons co-cultured with VPA-exposed astrocytes

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