In-vitro Recordings of Neural Magnetic Activity From the Auditory Brainstem Using Color Centers in Diamond: A Simulation Study
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In-vitro Recordings of Neural Magnetic Activity From the Auditory Brainstem Using Color Centers in Diamond : A Simulation Study. / Karadas, Mursel; Olsson, Christoffer; Winther Hansen, Nikolaj; Perrier, Jean-Francois; Webb, James Luke; Huck, Alexander; Andersen, Ulrik Lund; Thielscher, Axel.
In: Frontiers in Neuroscience, Vol. 15, 643614, 2021.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - In-vitro Recordings of Neural Magnetic Activity From the Auditory Brainstem Using Color Centers in Diamond
T2 - A Simulation Study
AU - Karadas, Mursel
AU - Olsson, Christoffer
AU - Winther Hansen, Nikolaj
AU - Perrier, Jean-Francois
AU - Webb, James Luke
AU - Huck, Alexander
AU - Andersen, Ulrik Lund
AU - Thielscher, Axel
PY - 2021
Y1 - 2021
N2 - Magnetometry based on nitrogen-vacancy (NV) centers in diamond is a novel technique capable of measuring magnetic fields with high sensitivity and high spatial resolution. With the further advancements of these sensors, they may open up novel approaches for the 2D imaging of neural signals in vitro. In the present study, we investigate the feasibility of NV-based imaging by numerically simulating the magnetic signal from the auditory pathway of a rodent brainstem slice (ventral cochlear nucleus, VCN, to the medial trapezoid body, MNTB) as stimulated by both electric and optic stimulation. The resulting signal from these two stimulation methods are evaluated and compared. A realistic pathway model was created based on published data of the neural morphologies and channel dynamics of the globular bushy cells in the VCN and their axonal projections to the principal cells in the MNTB. The pathway dynamics in response to optic and electric stimulation and the emitted magnetic fields were estimated using the cable equation. For simulating the optic stimulation, the light distribution in brain tissue was numerically estimated and used to model the optogenetic neural excitation based on a four state channelrhodopsin-2 (ChR2) model. The corresponding heating was also estimated, using the bio-heat equation and was found to be low (
AB - Magnetometry based on nitrogen-vacancy (NV) centers in diamond is a novel technique capable of measuring magnetic fields with high sensitivity and high spatial resolution. With the further advancements of these sensors, they may open up novel approaches for the 2D imaging of neural signals in vitro. In the present study, we investigate the feasibility of NV-based imaging by numerically simulating the magnetic signal from the auditory pathway of a rodent brainstem slice (ventral cochlear nucleus, VCN, to the medial trapezoid body, MNTB) as stimulated by both electric and optic stimulation. The resulting signal from these two stimulation methods are evaluated and compared. A realistic pathway model was created based on published data of the neural morphologies and channel dynamics of the globular bushy cells in the VCN and their axonal projections to the principal cells in the MNTB. The pathway dynamics in response to optic and electric stimulation and the emitted magnetic fields were estimated using the cable equation. For simulating the optic stimulation, the light distribution in brain tissue was numerically estimated and used to model the optogenetic neural excitation based on a four state channelrhodopsin-2 (ChR2) model. The corresponding heating was also estimated, using the bio-heat equation and was found to be low (
KW - cable equation
KW - neural magnetic field
KW - magnetometry
KW - NV centers
KW - Monte Carlo
KW - optogenetics
KW - fiber optics
KW - Kubelka-Munk model
KW - UNDERLYING OPTICAL STIMULATION
KW - POTASSIUM CHANNEL
KW - COCHLEAR NUCLEUS
KW - MEDIAL NUCLEUS
KW - TRAPEZOID BODY
KW - MOUSE CALYX
KW - KINETICS
KW - SYNAPSE
KW - LIGHT
KW - FIELD
U2 - 10.3389/fnins.2021.643614
DO - 10.3389/fnins.2021.643614
M3 - Journal article
C2 - 34054404
VL - 15
JO - Frontiers in Neuroscience
JF - Frontiers in Neuroscience
SN - 1662-4548
M1 - 643614
ER -
ID: 271752637