Subramanian Muthumeenakshi, Chiang Chia-Chu, Levi Cedric, Durand Dominique M
Neural Engineering Center, Department of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, 44106, USA.
Neural Engineering Center, Department of Biomedical Engineering, Case Western Reserve University, Cleveland, OH, 44106, USA.
Brain Stimul. 2025 Mar-Apr;18(2):225-234. doi: 10.1016/j.brs.2025.02.001. Epub 2025 Feb 10.
Neural activity such as theta waves, epileptic spikes and seizures can cross a physical transection using electric fields thus propagating by ephaptic coupling and independently of synaptic transmission. Recruitment of neurons in epilepsy occurs in part due to electric field coupling in addition to synaptic mechanisms. Hence, controlling the local electric field could suppress or cancel the generation of these epileptic events.
4-aminopyridine (4-AP) was used to induce spontaneous epileptic spikes and seizures in longitudinal hippocampal slices in-vitro. Two extracellular recording electrodes were placed in the tissue, one at the edge of the slice on the temporal side at the focus of the epileptic activity and the other on the septal side to record the propagation. Two stimulating electrodes were placed outside the slice at the edge of the focal zone. An extracellular voltage clamp circuit maintained the voltage within the focus at 0V with respect to the bath ground.
Experiments showed that 100 % of the epileptic activity originated at the temporal region and propagated to the septal region of the slices thereby establishing the existence of a focus in the temporal end of the tissue. The clamp achieved 100 % suppression of all seizure activity in the tissue with current amplitudes between 70 and 250 nA. No spikes or seizures were observed in either the focus or the septal region when the clamp was "on". When the clamp was turned off, both the spikes and seizure events recovered immediately.
The experiments show that controlling the extracellular voltage within a focus can prevent the generation and the propagation of epileptiform activity from the focus with very low amplitudes currents.
诸如θ波、癫痫棘波和癫痫发作等神经活动能够利用电场穿过物理横断区域,从而通过电突触耦合进行传播,且独立于突触传递。癫痫中神经元的募集部分是由于除了突触机制之外的电场耦合。因此,控制局部电场可以抑制或消除这些癫痫事件的产生。
使用4-氨基吡啶(4-AP)在体外纵向海马切片中诱导自发性癫痫棘波和癫痫发作。将两个细胞外记录电极置于组织中,一个位于癫痫活动焦点处颞侧切片边缘,另一个位于隔侧以记录传播情况。两个刺激电极置于切片外焦点区域边缘。一个细胞外电压钳电路将焦点内的电压相对于浴槽接地维持在0V。
实验表明,100%的癫痫活动起源于切片的颞区并传播至隔区,从而证实了组织颞端存在一个焦点。该钳制在70至250nA的电流幅度下实现了对组织中所有癫痫发作活动的100%抑制。当钳制开启时,在焦点或隔区均未观察到棘波或癫痫发作。当钳制关闭时,棘波和癫痫发作事件立即恢复。
实验表明,通过极低幅度的电流控制焦点内的细胞外电压可以防止癫痫样活动从焦点产生和传播。