SignificanceWe assess the feasibility of using diffuse reflectance spectroscopy (DRS) and coherent anti-Stokes Raman scattering spectroscopy (CARS) as optical tools for human brain tissue identification during deep brain stimulation (DBS) lead insertion, thereby providing a promising avenue for additional real-time neurosurgical guidance.AimWe developed a system that can acquire CARS and DRS spectra during the DBS surgery procedure to identify the tissue composition along the lead trajectory.ApproachDRS and CARS spectra were acquired using a custom-built optical probe integrated in a commercial DBS lead. The lead was inserted to target three specific regions in each of the brain hemispheres of a human cadaver. Spectra were acquired during the lead insertion at constant position increments. Spectra were analyzed to classify each spectrum as being from white matter (WM) or gray matter (GM). The results were compared with tissue classification performed on histological brain sections.ResultsDRS and CARS spectra obtained using the optical probe can identify WM and GM during DBS lead insertion. The tissue composition along the trajectory toward a specific target is unique and can be differentiated by the optical probe. Moreover, the results obtained with principal component analysis suggest that DRS might be able to detect the presence of blood due to the strong optical absorption of hemoglobin.ConclusionsIt is possible to use optical measurements from the DBS lead during surgery to identify WM and GM and possibly the presence of blood in human brain tissue. The proposed optical tool could inform the surgeon during the lead placement if the lead has reached the target as planned. Our tool could eventually replace microelectrode recordings, which would streamline the process and reduce surgery time. Further developments are required to fully integrate these tools into standard clinical procedures.
Deep brain stimulation (DBS) surgery is performed on patients suffering Parkinson’s disease for whom medication is no longer effective in relieving their motor symptoms. In this surgery, a stimulating electrode is implanted in a specific structure deep within the brain, delivering electrical impulses and thus reducing the motor symptoms. The success of the surgery is highly dependent on placing the electrode accurately in the targeted structure, typically the subthalamic nucleus (STN). We developed a DBS electrode that includes optical fibers to perform coherent anti-Stokes Raman scattering (CARS) spectroscopy and diffuse reflectance spectroscopy (DRS) during the electrode insertion in the brain. We were able to identify white and grey matter using principal component analysis (PCA), showing that spectroscopic measurements could be suitable for neuronavigation.
SignificanceTypical light sheet microscopes suffer from artifacts related to the geometry of the light sheet. One main inconvenience is the non-uniform thickness of the light sheet obtained with a Gaussian laser beam.AimWe developed a two-photon light sheet microscope that takes advantage of a thin and long Bessel-Gauss beam illumination to increase the sheet extent without compromising the resolution.ApproachWe use an axicon lens placed directly at the output of an amplified femtosecond laser to produce a long Bessel-Gauss beam on the sample. We studied the dopaminergic system and its projections in a whole cleared mouse brain.ResultsOur light sheet microscope allows an isotropic resolution of 2.4 μm in all three axes of the scanned volume while keeping a millimetric-sized field of view, and a fast acquisition rate of up to 34 mm2 / s. With slight modifications to the optical setup, the sheet extent can be increased to 6 mm.ConclusionThe proposed system’s sheet extent and resolution surpass currently available systems, enabling the fast imaging of large specimens.
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