In Vivo Voltage-Sensitive Dye Optical Functional Imaging of the Subcortical Brain

Author(s):  
Qinggong Tang ◽  
Vassiliy Tsytsarev ◽  
Chia-Pin Liang ◽  
Reha Erzurumlu ◽  
Yu Chen
2015 ◽  
Vol 5 (1) ◽  
Author(s):  
Qinggong Tang ◽  
Vassiliy Tsytsarev ◽  
Chia-Pin Liang ◽  
Fatih Akkentli ◽  
Reha S. Erzurumlu ◽  
...  

Author(s):  
David C. Ng ◽  
Takashi Tokuda ◽  
Keiichiro Kagawa ◽  
Hideki Tamura ◽  
Sadao Shiosaka ◽  
...  

Molecules ◽  
2021 ◽  
Vol 26 (6) ◽  
pp. 1614
Author(s):  
Ken-ichiro Matsumoto ◽  
James B. Mitchell ◽  
Murali C. Krishna

Radiation therapy is one of the main modalities to treat cancer/tumor. The response to radiation therapy, however, can be influenced by physiological and/or pathological conditions in the target tissues, especially by the low partial oxygen pressure and altered redox status in cancer/tumor tissues. Visualizing such cancer/tumor patho-physiological microenvironment would be a useful not only for planning radiotherapy but also to detect cancer/tumor in an earlier stage. Tumor hypoxia could be sensed by positron emission tomography (PET), electron paramagnetic resonance (EPR) oxygen mapping, and in vivo dynamic nuclear polarization (DNP) MRI. Tissue oxygenation could be visualized on a real-time basis by blood oxygen level dependent (BOLD) and/or tissue oxygen level dependent (TOLD) MRI signal. EPR imaging (EPRI) and/or T1-weighted MRI techniques can visualize tissue redox status non-invasively based on paramagnetic and diamagnetic conversions of nitroxyl radical contrast agent. 13C-DNP MRI can visualize glycometabolism of tumor/cancer tissues. Accurate co-registration of those multimodal images could make mechanisms of drug and/or relation of resulted biological effects clear. A multimodal instrument, such as PET-MRI, may have another possibility to link multiple functions. Functional imaging techniques individually developed to date have been converged on the concept of theranostics.


2007 ◽  
Vol 98 (1) ◽  
pp. 502-512 ◽  
Author(s):  
Michael T. Lippert ◽  
Kentaroh Takagaki ◽  
Weifeng Xu ◽  
Xiaoying Huang ◽  
Jian-Young Wu

We describe methods to achieve high sensitivity in voltage-sensitive dye (VSD) imaging from rat barrel and visual cortices in vivo with the use of a blue dye RH1691 and a high dynamic range imaging device (photodiode array). With an improved staining protocol and an off-line procedure to remove pulsation artifact, the sensitivity of VSD recording is comparable with that of local field potential recording from the same location. With this sensitivity, one can record from ∼500 individual detectors, each covering an area of cortical tissue 160 μm in diameter (total imaging field ∼4 mm in diameter) and a temporal resolution of 1,600 frames/s, without multiple-trial averaging. We can record 80–100 trials of intermittent 10-s trials from each imaging field before the VSD signal reduces to one half of its initial amplitude because of bleaching and wash-out. Taken together, the methods described in this report provide a useful tool for visualizing evoked and spontaneous waves from rodent cortex.


PLoS ONE ◽  
2011 ◽  
Vol 6 (10) ◽  
pp. e26158 ◽  
Author(s):  
Markus Rothermel ◽  
Benedict Shien Wei Ng ◽  
Agnieszka Grabska-Barwińska ◽  
Hanns Hatt ◽  
Dirk Jancke

Lab on a Chip ◽  
2017 ◽  
Vol 17 (22) ◽  
pp. 3935-3935
Author(s):  
Yongmin Cho ◽  
Daniel A. Porto ◽  
Hyundoo Hwang ◽  
Laura J. Grundy ◽  
William R. Schafer ◽  
...  

Correction for ‘Automated and controlled mechanical stimulation and functional imaging in vivo in C. elegans’ by Yongmin Cho et al., Lab Chip, 2017, 17, 2609–2618.


1999 ◽  
Author(s):  
Weisheng Zhang ◽  
Pamela Reilly-Contag ◽  
David K. Stevenson ◽  
Christopher H. Contag

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