Abstract

Non-invasive optical imaging of neuronal voltage response signals in live brains is constrained in depth by the optical diffusion limit, which is due primarily to optical scattering by brain tissues. Although photoacoustic tomography breaks this limit by exciting the targets with diffused photons and detecting the resulting acoustic responses, it has not been demonstrated as a modality for imaging voltage responses. In this communication, we report the first demonstration of photoacoustic voltage response imaging in both in vitro HEK-293 cell cultures and in vivo mouse brain surfaces. Using spectroscopic photoacoustic tomography at isosbestic wavelengths, we can separate voltage response signals and hemodynamic signals on live brain surfaces. By imaging HEK-293 cell clusters through 4.5 mm thick ex vivo rat brain tissue, we demonstrate photoacoustic tomography of cell membrane voltage responses beyond the optical diffusion limit. Although the current voltage dye does not immediately allow in vivo deep brain voltage response imaging, we believe our method opens up a feasible technical path for deep brain studies in the future.

Highlights

  • A human brain generates thoughts, perceptions, memories, actions, and emotions based on environments and experiences, while defining each individual person

  • We demonstrate the photoacoustic detection of Human embryonic kidney 293 (HEK-293) cell membrane voltages through 4.5 mm thick ex vivo rat brain tissue

  • Immediately allow in vivo deep brain voltage response imaging, we believe our method opens up a feasible technical path for deep brain studies in the future

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Summary

Introduction

A human brain generates thoughts, perceptions, memories, actions, and emotions based on environments and experiences, while defining each individual person. Microelectrodes and macro-electrodes are workhorses in recording neural voltage response signals and stimulating neural tissue[10, 11] in clinics and labs They are limited by the small number of practicable simultaneous recording points and they cannot interrogate tiny neuronal circuit components such as dendrites and axon terminals. PAT is a versatile optical imaging modality, its potential in imaging voltage responses of neuronal activities has never been explored. In this communication, for the first time, we demonstrate photoacoustic voltage response imaging contrast by using a non-radiative voltage sensor (dipicrylamine, or DPA for short). Immediately allow in vivo deep brain voltage response imaging, we believe our method opens up a feasible technical path for deep brain studies in the future

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