The State of the Dopaminergic and Glutamatergic Systems in the Valproic Acid Mouse Model of Autism Spectrum Disorder

Biomolecules. 2022 Nov 15;12(11):1691. doi: 10.3390/biom12111691.

Abstract

Autism Spectrum Disorder (ASD) is a progressive neurodevelopmental disorder mainly characterized by deficits in social communication and stereotyped behaviors and interests. Here, we aimed to investigate the state of several key players in the dopamine and glutamate neurotransmission systems in the valproic acid (VPA) animal model that was administered to E12.5 pregnant females as a single dose (450 mg/kg). We report no alterations in the number of mesencephalic dopamine neurons or in protein levels of tyrosine hydroxylase in either the striatum or the nucleus accumbens. In females prenatally exposed to VPA, levels of dopamine were slightly decreased while the ratio of DOPAC/dopamine was increased in the dorsal striatum, suggesting increased turn-over of dopamine tone. In turn, levels of D1 and D2 dopamine receptor mRNAs were increased in the nucleus accumbens of VPA mice suggesting upregulation of the corresponding receptors. We also report decreased protein levels of striatal parvalbumin and increased levels of p-mTOR in the cerebellum and the motor cortex of VPA mice. mRNA levels of mGluR1, mGluR4, and mGluR5 and the glutamate receptor subunits NR1, NR2A, and NR2B were not altered by VPA, nor were protein levels of NR1, NR2A, and NR2B and those of BDNF and TrkB. These findings are of interest as clinical trials aiming at the dopamine and glutamate systems are being considered.

Keywords: accumbens; autism spectrum disorder; cerebellum; dopamine; glutamate; mouse models; striatum; valproic acid.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autism Spectrum Disorder*
  • Disease Models, Animal
  • Dopamine / metabolism
  • Female
  • Glutamates
  • Mice
  • Pregnancy
  • Valproic Acid* / pharmacology

Substances

  • Valproic Acid
  • Dopamine
  • Glutamates

Grants and funding

The research leading to the results detailed in this manuscript received recurrent funding from Poitiers University and Inserm and specific funding from the Fondation pour la Recherche Médicale # DPP20151033963 (M.J.) and the CPER-FEDER program 2018–2022 (M.J.).