4.6 Article

Mesh-based Monte Carlo method for fibre-optic optogenetic neural stimulation with direct photon flux recording strategy

Journal

PHYSICS IN MEDICINE AND BIOLOGY
Volume 61, Issue 6, Pages 2265-2282

Publisher

IOP Publishing Ltd
DOI: 10.1088/0031-9155/61/6/2265

Keywords

light propagation in tissues; optogenetics; Monte Carlo simulation; photon migration; turbid media

Funding

  1. New Growth Engine Industry Project of the Ministry of Knowledge and Economy [10047579]
  2. National Research Foundation of Korea (NRF) - Korea government (MSIP) [2015R1A2A2A03005382]
  3. GIST Research Institute Project through GIST, Korea
  4. Korea Evaluation Institute of Industrial Technology (KEIT) [10047579] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  5. National Research Foundation of Korea [2015R1A2A2A03005382] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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We propose a Monte Carlo (MC) method based on a direct photon flux recording strategy using inhomogeneous, meshed rodent brain atlas. This MC method was inspired by and dedicated to fibre-optics-based optogenetic neural stimulations, thus providing an accurate and direct solution for light intensity distributions in brain regions with different optical properties. Our model was used to estimate the 3D light intensity attenuation for close proximity between an implanted optical fibre source and neural target area for typical optogenetics applications. Interestingly, there are discrepancies with studies using a diffusion-based light intensity prediction model, perhaps due to use of improper light scattering models developed for far-field problems. Our solution was validated by comparison with the gold-standard MC model, and it enabled accurate calculations of internal intensity distributions in an inhomogeneous near light source domain. Thus our strategy can be applied to studying how illuminated light spreads through an inhomogeneous brain area, or for determining the amount of light required for optogenetic manipulation of a specific neural target area.

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