School of Electrical and Computer Engineering, Purdue University, West Lafayette, IN, 47907, USA; Bindley Bioscience Center, Purdue University, West Lafayette, IN, 47907, USA.
Skirball Institute, Department of Neuroscience and Physiology, Department of Anesthesiology, New York University School of Medicine, New York, NY, 10016, USA.
Brain Stimul. 2022 Jan-Feb;15(1):190-196. doi: 10.1016/j.brs.2021.12.005. Epub 2021 Dec 21.
Neural modulation plays a major role in delineating the circuit mechanisms and serves as the cornerstone of neural interface technologies. Among the various modulation mechanisms, ultrasound enables noninvasive label-free deep access to mammalian brain tissue. To date, most if not all ultrasonic neural modulation implementations are based on ∼1 MHz carrier frequency. The long acoustic wavelength results in a spatially coarse modulation zone, often spanning over multiple function regions. The modulation of one function region is inevitably linked with the modulation of its neighboring regions. Moreover, the lack of in vivo cellular resolution cell-type-specific recording capabilities in most studies prevents the revealing of the genuine cellular response to ultrasound. To significantly increase the spatial resolution, we explored the application of high-frequency ultrasound. To investigate the neuronal response at cellular resolutions, we developed a dual-modality system combining in vivo two-photon calcium imaging and focused ultrasound modulation. The studies show that the ∼30 MHz ultrasound can suppress the neuronal activity in awake mice at 100-μm scale spatial resolutions, paving the way for high-resolution ultrasonic neural modulation. The dual-modality in vivo system validated through this study will serve as a general platform for studying the dynamics of various cell types in response to ultrasound.
神经调制在描绘电路机制方面起着重要作用,是神经接口技术的基石。在各种调制机制中,超声波能够实现对哺乳动物脑组织的非侵入性、无标记的深层访问。迄今为止,大多数(如果不是全部的话)超声神经调制的实现都基于约 1MHz 的载波频率。由于声波长较长,导致调制区域的空间分辨率粗糙,通常跨越多个功能区域。一个功能区域的调制不可避免地与相邻区域的调制相关联。此外,大多数研究中缺乏体内细胞分辨率的细胞类型特异性记录能力,这使得无法揭示超声波对真实细胞的反应。为了显著提高空间分辨率,我们探索了高频超声的应用。为了在细胞分辨率下研究神经元反应,我们开发了一种结合在体双光子钙成像和聚焦超声调制的双模态系统。研究表明,约 30MHz 的超声波可以在 100-μm 尺度的空间分辨率下抑制清醒小鼠的神经元活动,为高分辨率超声神经调制铺平了道路。通过这项研究验证的双模态在体系统将成为研究各种细胞类型对超声波反应的动力学的通用平台。