Detection of neural light-scattering activity in vivo: optical transmittance studies in the rat brain

0545856 - ÚI 2022 US eng J - Journal Article
Pan, W.J. - Lee, S. Y. - Billings, Jacob - Nezafati, M. - Majeed, W. - Buckley, E. - Keilholz, S.
Detection of neural light-scattering activity in vivo: optical transmittance studies in the rat brain.
Neuroimage. Roč. 179 (2018), s. 207-214. ISSN 1053-8119. E-ISSN 1095-9572
Keywords : imaging spectroscopy * water diffusion * cell-volume * signals * cortex * fmri * mri * Intrinsic optical signal * Neural scattering activity * Neurovascular coupling * Optical transmission measurement * In vivo
Impact factor: 5.812, year: 2018

Optical studies of ex vivo brain slices where blood is absent show that neural activity is accompanied by significant intrinsic optical signals (IOS) related to activity-dependent scattering changes in neural tissue. However, the neural scattering signals have been largely ignored in vivo in widely-used IOS methods where absorption contrast from hemoglobin was employed. Changes in scattering were observed on a time scale of seconds in previous brain slice IOS studies, similar to the time scale for the hemodynamic response. Therefore, potential crosstalk between the scattering and absorption changes may not be ignored if they have comparable contributions to IOS. In vivo, the IOS changes linked to neural scattering have been elusive. To isolate neural scattering signals in vivo, we employed 2 implantable optodes for small-separation (2 mm) transmission measurements of local brain tissue in anesthetized rats. This unique geometry enables us to separate neuronal activity-related changes in neural tissue scattering from changes in blood absorption based upon the direction of the signal change. The changes in IOS scattering and absorption in response to up-states of spontaneous neuronal activity in cortical or subcortical structures have strong correlation to local field potentials, but significantly different response latencies. We conclude that activity-dependent neural tissue scattering in vivo may be an additional source of contrast for functional brain studies that provides complementary information to other optical or MR-based systems that are sensitive to hemodynamic contrast.
Permanent Link: http://hdl.handle.net/11104/0322492