Kalirin is involved in epileptogenesis by modulating the activity of the Rac1 signaling pathway

J Chem Neuroanat. 2023 Sep:131:102289. doi: 10.1016/j.jchemneu.2023.102289. Epub 2023 May 17.

Abstract

Background and objective: Epilepsy is a common chronic brain disease. Despite the availability of various anti-seizure drugs, approximately 30 % of patients do not respond to treatment. Recent research suggests that Kalirin plays a role in regulating neurological function. However, the pathogenesis of Kalirin in epileptic seizures remains unclear. This study aims to investigate the role and mechanism of Kalirin in epileptogenesis.

Materials and methods: An epileptic model was induced by intraperitoneal injection of pentylenetetrazole (PTZ). Endogenous Kalirin was inhibited using shRNA. The expression of Kalirin, Rac1, and Cdc42 in the hippocampal CA1 region was measured using Western blotting. Spine and synaptic structures were examined using Golgi staining and electron microscopy. Moreover, the necrotic neurons in CA1 were examined using HE staining.

Results: The results indicated that the epileptic score increased in epileptic animals, while inhibition of Kalirin decreased the epileptic scores and increased the latent period of the first seizure attack. Inhibition of Kalirin attenuated the increases in Rac1 expression, dendritic spine density, and synaptic vesicle number in the CA1 region induced by PTZ. However, the increase in Cdc42 expression was not affected by the inhibition of Kalirin.

Conclusion: This study suggests that Kalirin is involved in the development of seizures by modulating the activity of Rac1, providing a novel anti-epileptic target.

Keywords: Dendritic spine; Epilepsy; Kalirin; Rac1; Synaptic Vesicles.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CA1 Region, Hippocampal / metabolism
  • Epilepsy* / metabolism
  • Guanine Nucleotide Exchange Factors* / metabolism
  • Neurons / metabolism
  • Pentylenetetrazole / metabolism
  • Protein Serine-Threonine Kinases* / metabolism
  • Signal Transduction* / physiology
  • rac1 GTP-Binding Protein* / metabolism

Substances

  • Pentylenetetrazole
  • rac1 GTP-Binding Protein
  • Protein Serine-Threonine Kinases
  • Guanine Nucleotide Exchange Factors