scholarly journals Recording neural activity in unrestrained animals with 3D tracking two photon microscopy

2017 ◽  
Author(s):  
Doycho Karagyozov ◽  
Mirna Mihovilovic Skanata ◽  
Amanda Lesar ◽  
Marc Gershow

Optical recordings of neural activity in behaving animals can reveal the neural correlates of decision making, but such recordings are compromised by brain motion that often accompanies behavior. Two-photon point scanning microscopy is especially sensitive to motion artifacts, and to date, two-photon recording of activity has required rigid mechanical coupling between the brain and microscope. To overcome these difficulties, we developed a two-photon tracking microscope with extremely low latency (360 μs) feedback implemented in hardware. We maintained continuous focus on neurons moving with velocities of 3 mm/s and accelerations of 1 m/s2 both in-plane and axially, allowing high-bandwidth measurements with modest excitation power. We recorded from motor- and inter-neurons in unrestrained freely behaving fruit fly larvae, correlating neural activity with stimulus presentation and behavioral outputs. Our technique can be extended to stabilize recordings in a variety of moving substrates.

Nano Letters ◽  
2013 ◽  
Vol 13 (3) ◽  
pp. 980-986 ◽  
Author(s):  
Bram van den Broek ◽  
Brian Ashcroft ◽  
Tjerk H. Oosterkamp ◽  
John van Noort

eLife ◽  
2020 ◽  
Vol 9 ◽  
Author(s):  
Tianyu Wang ◽  
Chunyan Wu ◽  
Dimitre G Ouzounov ◽  
Wenchao Gu ◽  
Fei Xia ◽  
...  

1300 nm three-photon calcium imaging has emerged as a useful technique to allow calcium imaging in deep brain regions. Application to large-scale neural activity imaging entails a careful balance between recording fidelity and perturbation to the sample. We calculated and experimentally verified the excitation pulse energy to achieve the minimum photon count required for the detection of calcium transients in GCaMP6s-expressing neurons for 920 nm two-photon and 1320 nm three-photon excitation. By considering the combined effects of in-focus signal attenuation and out-of-focus background generation, we quantified the cross-over depth beyond which three-photon microscopy outpeforms two-photon microscopy in recording fidelity. Brain tissue heating by continuous three-photon imaging was simulated with Monte Carlo method and experimentally validated with immunohistochemistry. Increased immunoreactivity was observed with 150 mW excitation power at 1 and 1.2 mm imaging depths. Our analysis presents a translatable model for the optimization of three-photon calcium imaging based on experimentally tractable parameters.


2016 ◽  
Vol 2016.28 (0) ◽  
pp. _1C21-1_-_1C21-4_
Author(s):  
Hiroshi TAKEDA ◽  
Ryo HOSHIKAWA ◽  
Hiroyuki TAKUWA ◽  
Bin JI ◽  
Makoto HIGUCHI ◽  
...  

Cell Reports ◽  
2018 ◽  
Vol 25 (5) ◽  
pp. 1371-1383.e10 ◽  
Author(s):  
Doycho Karagyozov ◽  
Mirna Mihovilovic Skanata ◽  
Amanda Lesar ◽  
Marc Gershow

2012 ◽  
Vol 39 (6) ◽  
pp. 505-512
Author(s):  
Run-Hua JIANG ◽  
Xiao-Hua LV ◽  
De-Rong LI ◽  
Ting-Wei QUAN ◽  
Xiu-Li LIU ◽  
...  

2010 ◽  
Vol 98 (3) ◽  
pp. 178a ◽  
Author(s):  
Bram van den Broek ◽  
Tjerk H. Oosterkamp ◽  
John van Noort

2016 ◽  
Vol 54 (12) ◽  
pp. 1343-1404
Author(s):  
A Ghallab ◽  
R Reif ◽  
R Hassan ◽  
AS Seddek ◽  
JG Hengstler

ACS Omega ◽  
2020 ◽  
Author(s):  
Kazushi Yamaguchi ◽  
Kohei Otomo ◽  
Yuichi Kozawa ◽  
Motosuke Tsutsumi ◽  
Tomoko Inose ◽  
...  

2021 ◽  
Vol 18 (2) ◽  
pp. 220-220
Author(s):  
Weijian Zong ◽  
Runlong Wu ◽  
Shiyuan Chen ◽  
Junjie Wu ◽  
Hanbin Wang ◽  
...  

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