Abstract

Functional mapping of brain activity is important in elucidating how neural networks operate in the living brain. The whisker sensory system of rodents is an excellent model to study peripherally evoked neural activity in the central nervous system. Each facial whisker is represented by discrete modules of neurons all along the pathway leading to the neocortex. These modules are called “barrels” in layer 4 of the primary somatosensory cortex. Their location (approximately 300–500 μm below cortical surface) allows for convenient imaging of whisker-evoked neural activity in vivo. Fluorescence laminar optical tomography (FLOT) provides depth-resolved fluorescence molecular information with an imaging depth of a few millimeters. Angled illumination and detection configurations can improve both resolution and penetration depth. We applied angled FLOT (aFLOT) to record 3D neural activities evoked in the whisker system of mice by deflection of a single whisker in vivo. A 100 μm capillary and a pair of microelectrodes were inserted to the mouse brain to test the capability of the imaging system. The results show that it is possible to obtain 3D functional maps of the sensory periphery in the brain. This approach can be broadly applicable to functional imaging of other brain structures.

Highlights

  • Visualization of evoked and spontaneous neuronal activity in vivo is of great importance for understanding brain functions

  • In this paper, combining angled FLOT (aFLOT) with voltage-sensitive dyes (VSDs), we present 3D neural activities evoked in the whisker barrel cortex of mice by deflection of a single whisker in vivo with 5 ms temporal resolution

  • We have demonstrated that it is possible to detect the 3D neural activities by deflection of a single whisker using non-contact optical measurements of the mouse brain in vivo

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Summary

Sensitive Dye Imaging of Brain

Activation received: 10 November 2015 accepted: 14 April 2016 Published: 29 April 2016. The two green rods in the 3D OCT image are the electrodes recorded by OCT and the orange ones are the aFLOT-reconstructed changes in fluorescence (Δ F/F(%), ordinate) in response to electrical stimulation at different time points. Changes in fluorescence (ΔF/F(%), ordinate) in response to the C2 whisker stimulation reconstructed by the aFLOT system in different depths. Compared to neural responses in XY plane, XZ cross-section provides us with a new perspective to investigate the neural activities at different time points

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