Effect of Vagus Nerve Stimulation on the GASH/Sal Audiogenic-Seizure-Prone Hamster.
Jaime Gonçalves-SánchezConsuelo SanchoDolores E LópezOrlando CastellanoMaria-Begoña Garcia-CenadorGabriel Servilha-MenezesJuan Manuel Corchado RodríguezNorberto García-CairascoJesús M Gonçalves-EstellaPublished in: International journal of molecular sciences (2023)
Vagus nerve stimulation (VNS) is an adjuvant neuromodulation therapy for the treatment of refractory epilepsy. However, the mechanisms behind its effectiveness are not fully understood. Our aim was to develop a VNS protocol for the Genetic Audiogenic Seizure Hamster from Salamanca (GASH/Sal) in order to evaluate the mechanisms of action of the therapy. The rodents were subject to VNS for 14 days using clinical stimulation parameters by implanting a clinically available neurostimulation device or our own prototype for laboratory animals. The neuroethological assessment of seizures and general behavior were performed before surgery, and after 7, 10, and 14 days of VNS. Moreover, potential side effects were examined. Finally, the expression of 23 inflammatory markers in plasma and the left-brain hemisphere was evaluated. VNS significantly reduced seizure severity in GASH/Sal without side effects. No differences were observed between the neurostimulation devices. GASH/Sal treated with VNS showed statistically significant reduced levels of interleukin IL-1β, monocyte chemoattractant protein MCP-1, matrix metalloproteinases (MMP-2, MMP-3), and tumor necrosis factor TNF-α in the brain. The described experimental design allows for the study of VNS effects and mechanisms of action using an implantable device. This was achieved in a model of convulsive seizures in which VNS is effective and shows an anti-inflammatory effect.
Keyphrases
- temporal lobe epilepsy
- randomized controlled trial
- anti inflammatory
- rheumatoid arthritis
- minimally invasive
- systematic review
- early stage
- white matter
- dendritic cells
- endothelial cells
- stem cells
- mesenchymal stem cells
- dna methylation
- binding protein
- risk assessment
- acute coronary syndrome
- genome wide
- small molecule
- multiple sclerosis
- coronary artery bypass
- protein protein