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用于帕金森病大鼠高精度深部脑图谱绘制和神经调节的柔性石墨烯基神经技术。

Flexible graphene-based neurotechnology for high-precision deep brain mapping and neuromodulation in Parkinsonian rats.

作者信息

Ria Nicola, Eladly Ahmed, Masvidal-Codina Eduard, Illa Xavi, Guimerà Anton, Hills Kate, Garcia-Cortadella Ramon, Duvan Fikret Taygun, Flaherty Samuel M, Prokop Michal, Wykes Rob C, Kostarelos Kostas, Garrido Jose A

机构信息

Catalan Institute of Nanoscience and Nanotechnology (ICN2), CSIC and BIST, Campus UAB, Bellaterra, Spain.

University of Manchester, Center for Nanotechnology in Medicine & Division of Neuroscience, London, UK.

出版信息

Nat Commun. 2025 Mar 25;16(1):2891. doi: 10.1038/s41467-025-58156-z.

Abstract

Deep brain stimulation (DBS) is a neuroelectronic therapy for the treatment of a broad range of neurological disorders, including Parkinson's disease. Current DBS technologies face important limitations, such as large electrode size, invasiveness, and lack of adaptive therapy based on biomarker monitoring. In this study, we investigate the potential benefits of using nanoporous reduced graphene oxide (rGO) technology in DBS, by implanting a flexible high-density array of rGO microelectrodes (25 µm diameter) in the subthalamic nucleus (STN) of healthy and hemi-parkinsonian rats. We demonstrate that these microelectrodes record action potentials with a high signal-to-noise ratio, allowing the precise localization of the STN and the tracking of multiunit-based Parkinsonian biomarkers. The bidirectional capability to deliver high-density focal stimulation and to record high-fidelity signals unlocks the visualization of local neuromodulation of the multiunit biomarker. These findings demonstrate the potential of bidirectional high-resolution neural interfaces to investigate closed-loop DBS in preclinical models.

摘要

深部脑刺激(DBS)是一种用于治疗多种神经系统疾病(包括帕金森病)的神经电子疗法。当前的DBS技术面临重要局限性,如电极尺寸大、具有侵入性以及缺乏基于生物标志物监测的适应性治疗。在本研究中,我们通过将柔性高密度氧化石墨烯还原(rGO)微电极阵列(直径25μm)植入健康大鼠和半帕金森病大鼠的丘脑底核(STN),研究在DBS中使用纳米多孔rGO技术的潜在益处。我们证明,这些微电极能够以高信噪比记录动作电位,从而实现STN的精确定位以及基于多单元的帕金森病生物标志物的追踪。提供高密度聚焦刺激和记录高保真信号的双向能力开启了多单元生物标志物局部神经调节可视化的大门。这些发现证明了双向高分辨率神经接口在临床前模型中研究闭环DBS的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa46/11937542/63838b93234b/41467_2025_58156_Fig1_HTML.jpg

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