Short-term mastication after weaning upregulates GABAergic signalling and reduces dendritic spine in thalamus

Biochem Biophys Res Commun. 2018 Apr 6;498(3):621-626. doi: 10.1016/j.bbrc.2018.03.032. Epub 2018 Mar 11.

Abstract

Mastication enhances brain function and mental health, but little is known about the molecular mechanisms underlying the effects of mastication on neural development in early childhood. Therefore, we analysed the gene expression in juvenile neural circuits in rats fed with a soft or chow diet immediately after weaning. We observed that the gene expression patterns in the thalamus varied depending on the diet. Furthermore, gene ontology analysis revealed that two terms were significantly enhanced: chemical synaptic transmission and positive regulation of dendritic spine morphogenesis. With respect to chemical synaptic transmission, glutamate decarboxylase and GABA receptors were upregulated in the chow diet group. The related genes, including vesicular GABA transporter, were also upregulated, suggesting that mastication activates GABAergic signalling. With respect to dendritic spine morphogenesis, Ingenuity Pathway Analysis predicted fewer extension of neurites and neurons and fewer number of branches in the chow diet group. The numbers of spines in the ventral posterolateral and posteromedial regions were significantly decreased. These results suggest that mastication in the early developing period upregulates GABAergic signalling genes, with a decrease of spines in the thalamus.

Keywords: Dendritic spine; GABA; Mastication; Thalamus; Transcriptome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animal Feed / analysis
  • Animals
  • Dendritic Spines / genetics
  • Dendritic Spines / physiology*
  • Dendritic Spines / ultrastructure
  • GABA Plasma Membrane Transport Proteins / genetics
  • GABA Plasma Membrane Transport Proteins / metabolism
  • Gene Expression Regulation, Developmental
  • Glutamate Decarboxylase / genetics
  • Glutamate Decarboxylase / metabolism
  • Male
  • Mastication*
  • Neurogenesis
  • Rats
  • Rats, Wistar
  • Receptors, GABA / genetics
  • Receptors, GABA / metabolism
  • Signal Transduction*
  • Synaptic Transmission
  • Thalamus / growth & development
  • Thalamus / physiology*
  • Transcriptome
  • Up-Regulation
  • Weaning
  • gamma-Aminobutyric Acid / genetics
  • gamma-Aminobutyric Acid / metabolism*

Substances

  • GABA Plasma Membrane Transport Proteins
  • Receptors, GABA
  • gamma-Aminobutyric Acid
  • Glutamate Decarboxylase