4.7 Article

Changes in Metabotropic Glutamate Receptor Gene Expression in Rat Brain in a Lithium-Pilocarpine Model of Temporal Lobe Epilepsy

Journal

Publisher

MDPI
DOI: 10.3390/ijms23052752

Keywords

temporal lobe epilepsy; metabotropic glutamate receptor; RT-qPCR; lithium-pilocarpine model; hippocampus; temporal cortex

Funding

  1. IEPhB Research Program [075-00408-21-00]
  2. IEPhB Research Resource Center

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This study analyzed the changes in gene expression of mGluR subtypes in different brain regions during the latent and chronic phases of a lithium-pilocarpine model of epilepsy. The results showed region- and phase-specific changes in expression, with increased mGluR5 mRNA levels and decreased expression of group III genes during the latent phase. Most of the changes in expression detected in the latent stage were absent in the chronic stage, except for reduced mGluR8 mRNA production in the hippocampus. The study suggested that agonists of group III mGluRs are the most promising targets for preventing epilepsy.
Preventing epileptogenesis in people at risk is an unmet medical need. Metabotropic glutamate receptors (mGluRs) are promising targets for such therapy. However, drugs acting on mGluRs are not used in the clinic due to limited knowledge of the involvement of mGluRs in epileptogenesis. This study aimed to analyze the changes in gene expression of mGluR subtypes (1-5, 7, 8) in various rat brain regions in the latent and chronic phases of a lithium-pilocarpine model of epilepsy. For this study, multiplex test systems were selected and optimized to analyze mGluR gene expression using RT-qPCR. Region- and phase-specific changes in expression were revealed. During the latent phase, mGluR5 mRNA levels were increased in the dorsal and ventral hippocampus, and expression of group III genes was decreased in the hippocampus and temporal cortex, which could contribute to epileptogenesis. Most of the changes in expression detected in the latent stage were absent in the chronic stage, but mGluR8 mRNA production remained reduced in the hippocampus. Moreover, we found that gene expression of group II mGluRs was altered only in the chronic phase. The study deepened our understanding of the mechanisms of epileptogenesis and suggested that agonists of group III mGluRs are the most promising targets for preventing epilepsy.

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