Medtronic Neuromodulation, Minneapolis, MN, USA.
Medtronic Neuromodulation, Minneapolis, MN, USA.
Brain Res. 2025 Jan 1;1846:149233. doi: 10.1016/j.brainres.2024.149233. Epub 2024 Sep 12.
Recent reports have described stimulation evoked resonant neural activity (ERNA) recorded in the subthalamic nucleus (STN) and globus pallidus internus (GPi) of patients during Deep Brain Stimulation (DBS) surgery. The constraints imposed during intraoperative recordings in patients limit the opportunity for in-depth study of new findings such as ERNA. In this pilot study, we leverage a large animal model to focus on detailed characterization of ERNA. Bilateral DBS leads were implanted in the STN in three ovine subjects and externalized for chronic use with custom stimulation and recording circuitry. ERNA was reliably recorded from the STN region in all three subjects with distinct specificity to recording and stimulation sites/contacts. Basic neural response characteristics such as input/output behavior, frequency response and strength/duration curves were evaluated. ERNA amplitude was highly dependent upon stimulation frequency, due to the interaction of the underlying resonant activity and the evoked response from each stimulus pulse. The results could be predicted by a mathematical model of constructive/destructive phase interference, and importantly, the evoked response latency. Significant time dependent dynamics in these evoked potentials were observed, which will be critically important to understand for future clinical applications. Based upon these recordings from leads in the STN region of healthy ovine subjects, these data confirm that DBS evokes high frequency resonant activity in the basal ganglia network. The clinical utility of ERNA remains to be demonstrated, but its direct association with DBS therapy makes it an interesting biomarker for potential use in contact selection and closed loop therapy.
最近的报告描述了在深部脑刺激 (DBS) 手术中记录到的患者丘脑底核 (STN) 和苍白球 internus (GPi) 中的刺激诱发共振神经活动 (ERNA)。患者术中记录期间施加的限制限制了对 ERNA 等新发现的深入研究机会。在这项初步研究中,我们利用大动物模型专注于 ERNA 的详细特征描述。在三个绵羊受试者中双侧植入 STN 的 DBS 导联,并通过定制的刺激和记录电路将其引出用于慢性使用。在所有三个受试者中都可靠地从 STN 区域记录到 ERNA,其特异性明显针对记录和刺激部位/触点。评估了基本的神经反应特征,如输入/输出行为、频率响应和强度/持续时间曲线。由于潜在的共振活动与每个刺激脉冲的诱发反应之间的相互作用,ERNA 幅度高度依赖于刺激频率。结果可以通过建设性/破坏性相位干扰的数学模型进行预测,重要的是,诱发反应潜伏期。观察到这些诱发电位中存在显著的时间相关动力学,这对于未来的临床应用至关重要。基于健康绵羊受试者 STN 区域导联的这些记录,这些数据证实 DBS 会在基底神经节网络中引发高频共振活动。ERNA 的临床效用仍有待证明,但它与 DBS 治疗的直接关联使其成为潜在应用于触点选择和闭环治疗的有趣生物标志物。