Transcriptome of the Wistar audiogenic rat (WAR) strain following audiogenic seizures

Epilepsy Res. 2018 Nov:147:22-31. doi: 10.1016/j.eplepsyres.2018.08.010. Epub 2018 Aug 29.

Abstract

The Wistar Audiogenic Rat (WAR) is a model whose rats are predisposed to develop seizures following acoustic stimulation. We aimed to establish the transcriptional profile of the WAR model, searching for genes that help in understanding the molecular mechanisms involved in the predisposition and seizures expression of this strain. RNA-Seq of the corpora quadrigemina of WAR and Wistar rats subjected to acoustic stimulation revealed 64 genes differentially regulated in WAR. We validated twelve of these genes by qPCR in stimulated and naive (non-stimulated) WAR and Wistar rats. Among these, Acsm3 was upregulated in WAR in comparison with both control groups. In contrast, Gpr126 and Rtel1 were downregulated in naive and stimulated WAR rats in comparison with the Wistar controls. Qdpr was upregulated only in stimulated WAR rats that exhibited audiogenic seizures. Our data show that there are genes with differential intrinsic regulation in the WAR model and that seizures can alter gene regulation. We identified new genes that might be involved in the epileptic phenotype and comorbidities of the WAR model.

Keywords: Audiogenic epilepsy; RNA-Seq; Seizure; Transcriptome; WAR.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acoustic Stimulation / adverse effects
  • Animals
  • Disease Models, Animal
  • Epilepsy, Reflex / genetics*
  • Epilepsy, Reflex / pathology*
  • Epilepsy, Reflex / physiopathology*
  • Gene Expression Profiling
  • Kindling, Neurologic / physiology
  • Male
  • Principal Component Analysis
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Wistar
  • Receptors, G-Protein-Coupled / genetics
  • Receptors, G-Protein-Coupled / metabolism*
  • Spectrophotometry
  • Tectum Mesencephali / metabolism
  • Tectum Mesencephali / physiopathology*
  • Transcriptome / physiology*

Substances

  • RNA, Messenger
  • Receptors, G-Protein-Coupled