Evaluation of skull optical clearing process for longitudinal non invasive optical imaging

We have evaluated in vitro and in vivo the efficiency and practicability of reversible optical clearing of the skull for minimally invasive, longitudinal imaging of the rodent brain. Firstly, in vitro experiments have been conducted on resected mice skulls to evaluate the efficiency of the optical clarification process using different optical clearing agents. On the basis of recent literature, we have evaluated in vitro different optical clearing processes: (i) the direct application of PEG400; (ii) sequential EDTA and glycerol application and (iii) application of a solution of urea dissolved in ethanol. First, the time course of the clarification of the skull has been monitored quantitatively. We have carried out photometry experiments at 633 nm using a two integrating spheres system to characterize the total transmittance and reflectance of the mice skull samples. The evaluation of the optical transmission coefficient at 1300 nm was also obtained at different time points of the clearing process using sequential optical coherent tomography (OCT) imaging of the skull samples during the clearing process. Second, in vivo evaluation was carried out for repeated transcranial mapping of brain blood flow after optical clarification of the skull. Relative blood flow maps were obtained from multiple exposure laser speckle imaging. Third, post-mortem analysis of the toxicity of the chemicalstopical application was evaluated using immunohistochemistry to asses eventual cells death and inflammation. Overall our results show that in vivo brain imaging in mice could benefit from in vivo optical clearing. Yet, the use of optical clearing agents in vivo requires a proper evaluation of their efficiency, practicability of their use and potential toxicity to the tissues, especially for long term longitudinal studies.

[1]  H. Gurden,et al.  Visualizing odor representation in the brain: a review of imaging techniques for the mapping of sensory activity in the olfactory glomeruli , 2011, Cellular and Molecular Life Sciences.

[2]  Mildred S. Cano-Velázquez,et al.  Evaluation of a transparent cranial implant as a permanent window for cerebral blood flow imaging. , 2018, Biomedical optics express.

[3]  Leila Ghanbari,et al.  Cortex-wide neural interfacing via transparent polymer skulls , 2018, Nature Communications.

[4]  Hongkui Zeng,et al.  Long-Term Optical Access to an Estimated One Million Neurons in the Live Mouse Cortex. , 2016, Cell reports.

[5]  Anna Devor,et al.  Determination of optimal exposure time for imaging of blood flow changes with laser speckle contrast imaging. , 2005, Applied optics.

[6]  David Kleinfeld,et al.  Chronic optical access through a polished and reinforced thinned skull. , 2010, Nature methods.

[7]  Valery V Tuchin,et al.  Measurement of tissue optical properties in the context of tissue optical clearing , 2018, Journal of biomedical optics.

[8]  Soleimanzad Haleh,et al.  Optical properties of mice skull bone in the 455- to 705-nm range. , 2017, Journal of biomedical optics.

[9]  Dan Zhu,et al.  Quantitative evaluation of SOCS-induced optical clearing efficiency of skull. , 2015, Quantitative imaging in medicine and surgery.

[10]  A. Grinvald,et al.  A tandem-lens epifluorescence macroscope: Hundred-fold brightness advantage for wide-field imaging , 1991, Journal of Neuroscience Methods.

[11]  Henry Pinkard,et al.  Advanced methods of microscope control using μManager software. , 2014, Journal of biological methods.

[12]  Jian Wang,et al.  Longitudinal volume changes of hippocampal subfields and cognitive decline in Parkinson's disease. , 2020, Quantitative imaging in medicine and surgery.

[13]  Olivier Lefebvre,et al.  Multiple speckle exposure imaging for the study of blood flow changes induced by functional activation of barrel cortex and olfactory bulb in mice , 2019, Neurophotonics.

[14]  Shigeo Okabe,et al.  Evaluation of cranial window types for in vivo two-photon imaging of brain microstructures. , 2014, Microscopy.

[15]  Demetris K. Roumis,et al.  Removable cranial windows for long-term imaging in awake mice , 2014, Nature Protocols.

[16]  Andrew C. N. Chen,et al.  Intact skull chronic windows for mesoscopic wide-field imaging in awake mice , 2016, Journal of Neuroscience Methods.

[17]  Q. Luo,et al.  A large, switchable optical clearing skull window for cerebrovascular imaging , 2018, Theranostics.

[18]  Andrew K. Dunn,et al.  Quantitative imaging of ischemic stroke through thinned skull in mice with Multi Exposure Speckle Imaging , 2010, Biomedical optics express.

[19]  Ruikang K. Wang,et al.  Application of Thinned-Skull Cranial Window to Mouse Cerebral Blood Flow Imaging Using Optical Microangiography , 2014, PloS one.

[20]  J. Goodman Statistical Properties of Laser Speckle Patterns , 1963 .

[21]  Shuang Chang,et al.  Review of methods and applications of attenuation coefficient measurements with optical coherence tomography , 2019, Journal of biomedical optics.