Department of Cellular Biology and Pathology, School of Medicine, University of Salamanca, 37007 Salamanca, Spain.
Institute for Biomedical Research of Salamanca (IBSAL), 37007 Salamanca, Spain.
Int J Mol Sci. 2023 Dec 20;25(1):91. doi: 10.3390/ijms25010091.
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.
迷走神经刺激(VNS)是一种辅助神经调节疗法,用于治疗难治性癫痫。然而,其有效性背后的机制尚不完全清楚。我们的目的是为来自萨拉曼卡的遗传性听觉癫痫仓鼠(GASH/Sal)开发 VNS 方案,以评估该疗法的作用机制。通过植入临床可用的神经刺激设备或我们自己的实验室动物原型,对啮齿动物进行 14 天的 VNS。在手术前和 VNS 后的第 7、10 和 14 天,对癫痫发作和一般行为进行神经行为学评估。此外,还检查了潜在的副作用。最后,评估了血浆和左脑半球中 23 种炎症标志物的表达。VNS 可显著降低 GASH/Sal 的癫痫严重程度,且无副作用。两种神经刺激设备之间没有差异。接受 VNS 治疗的 GASH/Sal 在大脑中显示出白细胞介素 IL-1β、单核细胞趋化蛋白 MCP-1、基质金属蛋白酶(MMP-2、MMP-3)和肿瘤坏死因子 TNF-α的水平显著降低。所描述的实验设计允许使用植入式设备研究 VNS 效应和作用机制。在一种有效的癫痫发作模型中实现了这一点,并显示出抗炎作用。