TY - JOUR
T1 - INS-fOCT
T2 - A label-free, all-optical method for simultaneously manipulating and mapping brain function
AU - Zhang, Ying
AU - Yao, Lin
AU - Yang, Fen
AU - Yang, Shanshan
AU - Edathodathil, Akshay
AU - Xi, Wang
AU - Roe, Anna Wang
AU - Li, Peng
N1 - Funding Information:
This work was supported by the Zhejiang Provincial Natural Science Foundation of China (LR19F050002) (to P.L.), the National Key Research and Development Program of China 2018YFA0701400 (to A.W.R.), the National Natural Science Foundation of China (81430010 and 31627802) (to A.W.R.), the Key Research and Development Program of Zhejiang province (2020C03004) (to A.W.R.), Zhejiang Lab (2018EB0ZX01) (to P.L.), the Fundamental Research Funds for the Central Universities (2018FZA5003) (to P.L.). We thank Song Xuemei and Hu Jiaming for technical assistance.
Publisher Copyright:
© The Authors. Published by SPIE under a Creative Commons Attribution 4.0 Unported License. Distribution or reproduction of this work in whole or in part requires full attribution of the original publication, including its DOI.
PY - 2020/1/1
Y1 - 2020/1/1
N2 - Significance: Current approaches to stimulating and recording from the brain have combined electrical or optogenetic stimulation with recording approaches, such as two-photon, electrophysiology (EP), and optical intrinsic signal imaging (OISI). However, we lack a label-free, all-optical approach with high spatial and temporal resolution. Aim: To develop a label-free, all-optical method that simultaneously manipulates and images brain function using pulsed near-infrared light (INS) and functional optical coherence tomography (fOCT), respectively. Approach: We built a coregistered INS, fOCT, and OISI system. OISI and EP recordings were employed to validate the fOCT signals. Results: The fOCT signal was reliable and regional, and the area of fOCT signal corresponded with the INS-activated region. The fOCT signal was in synchrony with the INS onset time with a delay of âˆ1/430 ms. The magnitude of fOCT signal exhibited a linear correlation with the INS radiant exposure. The significant correlation between the fOCT signal and INS was further supported by OISI and EP recordings. Conclusions: The proposed fiber-based, all-optical INS-fOCT method allows simultaneous stimulation and mapping without the risk of interchannel cross-talk and the requirement of contrast injection and viral transfection and offers a deep penetration depth and high resolution.
AB - Significance: Current approaches to stimulating and recording from the brain have combined electrical or optogenetic stimulation with recording approaches, such as two-photon, electrophysiology (EP), and optical intrinsic signal imaging (OISI). However, we lack a label-free, all-optical approach with high spatial and temporal resolution. Aim: To develop a label-free, all-optical method that simultaneously manipulates and images brain function using pulsed near-infrared light (INS) and functional optical coherence tomography (fOCT), respectively. Approach: We built a coregistered INS, fOCT, and OISI system. OISI and EP recordings were employed to validate the fOCT signals. Results: The fOCT signal was reliable and regional, and the area of fOCT signal corresponded with the INS-activated region. The fOCT signal was in synchrony with the INS onset time with a delay of âˆ1/430 ms. The magnitude of fOCT signal exhibited a linear correlation with the INS radiant exposure. The significant correlation between the fOCT signal and INS was further supported by OISI and EP recordings. Conclusions: The proposed fiber-based, all-optical INS-fOCT method allows simultaneous stimulation and mapping without the risk of interchannel cross-talk and the requirement of contrast injection and viral transfection and offers a deep penetration depth and high resolution.
KW - functional imaging
KW - functional optical coherence tomography
KW - infrared neural stimulation
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U2 - 10.1117/1.NPh.7.1.015014
DO - 10.1117/1.NPh.7.1.015014
M3 - Article
AN - SCOPUS:85083240668
SN - 2329-4248
VL - 7
JO - Neurophotonics
JF - Neurophotonics
IS - 1
M1 - 015014
ER -