High-Throughput Microelectrode Arrays for Precise Functional Localization of the Globus Pallidus Internus

Author:

Zhu Yuxin12,Jing Luyi12,Hu Ruilin12,Mo Fan12,Jia Qianli12,Yang Gucheng12,Xu Zhaojie12,Han Meiqi12,Wang Mixia12,Cai Xinxia12,Luo Jinping12ORCID

Affiliation:

1. State Key Laboratory of Transducer Technology, Aerospace Information Research Institute, Chinese Academy of Sciences, Beijing 100190, China.

2. School of Electronics, Electrical and Communication Engineering, University of Chinese Academy of Sciences, Beijing 100049, China.

Abstract

The globus pallidus internus (GPi) was considered a common target for stimulation in Parkinson’s disease (PD). Located deep in the brain and of small size, pinpointing it during surgery is challenging. Multi-channel microelectrode arrays (MEAs) can provide micrometer-level precision functional localization, which can maximize the surgical outcome. In this paper, a 64-channel MEA modified by platinum nanoparticles with a detection site impedance of 61.1 kΩ was designed and prepared, and multiple channels could be synchronized to cover the target brain region and its neighboring regions so that the GPi could be identified quickly and accurately. The results of the implant trajectory indicate that, compared to the control side, there is a reduction in local field potential (LFP) power in multiple subregions of the upper central thalamus on the PD-induced side, while the remaining brain regions exhibit an increasing trend. When the MEA tip was positioned at 8,700 μm deep in the brain, the various characterizations of the spike signals, combined with the electrophysiological characteristics of the β-segmental oscillations in PD, enabled MEAs to localize the GPi at the single-cell level. More precise localization could be achieved by utilizing the distinct characteristics of the internal capsule (ic), the thalamic reticular nucleus (Rt), and the peduncular part of the lateral hypothalamus (PLH) brain regions, as well as the relative positions of these brain structures. The MEAs designed in this study provide a new detection method and tool for functional localization of PD targets and PD pathogenesis at the cellular level.

Funder

the National Natural Science Foundation of China

the National Key Research and Development Program of China

Major Program of Scientific and Technical Innovation 2030

Publisher

American Association for the Advancement of Science (AAAS)

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