Abstract
Over the past decade, optical methods have emerged for modulating brain functions as an alternative to electrical stimulation. Among various optical techniques, infrared neural stimulation has been effective via a thermal mechanism enabling focused and noninvasive stimulation without any genetic manipulation, but it results in bulk heating of neural tissue. Recently, it has been shown that neural cells can be activated more efficiently by pulsed near-infrared (NIR) light delivered to gold nanorods (GNRs) near the neural cells. Despite its potential, however, the biophysical mechanism underlying this GNR-enhanced NIR stimulation has not been clearly explained yet. Here, we propose an integrative and quantitative model to elucidate the mechanism by modeling heat generated from interaction between NIR light and GNRs, the temperature-dependent ion channels (transient receptor potential vanilloid 1; TRPV1) in the neuronal membrane, and a heat-induced capacitive current through the membrane. Our results show that NIR pulses induce abrupt temperature elevation near the neuronal membrane and lead to both the TRPV1-channel and capacitive currents. Both current sources synergistically increase the membrane potential and elicit an action potential, and which mechanism is dominant depends on conditions such as the laser pulse duration and TRPV1 channel density. Although the TRPV1 mechanism dominates in most cases we tested, the capacitive current makes a larger contribution when a very short laser pulse is illuminated on neural cells with relatively low TRPV1 channel densities.
Original language | English |
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Pages (from-to) | 1481-1497 |
Number of pages | 17 |
Journal | Biophysical Journal |
Volume | 115 |
Issue number | 8 |
DOIs | |
State | Published - 16 Oct 2018 |
Bibliographical note
Funding Information:This work was supported by National Institutes of Health/National Institute of Biomedical Imaging and Bioengineering R00-EB014879 , the Brain Korea 21 Plus Project , the Department of Electrical and Computer Engineering, Seoul National University in 2018 , and a grant to Control of Animal Brain using MEMS Chip funded by Defense Acquisition Program Administration ( UD170030ID ). This work was also supported in part by the National Research Foundation of Korea ( 2017R1A2B4012428 ) and the Bio & Medical Technology Development Program and Global Frontier Project of the National Research Foundation of Korea funded by the Ministry of Science & ICT ( CISS-2012M3A6A054204 , NRF-2017M3A9E2062685 , 2018M3C1B8016147 ).
Funding Information:
This work was supported by National Institutes of Health/National Institute of Biomedical Imaging and Bioengineering R00-EB014879, the Brain Korea 21 Plus Project, the Department of Electrical and Computer Engineering, Seoul National University in 2018, and a grant to Control of Animal Brain using MEMS Chip funded by Defense Acquisition Program Administration (UD170030ID). This work was also supported in part by the National Research Foundation of Korea (2017R1A2B4012428) and the Bio & Medical Technology Development Program and Global Frontier Project of the National Research Foundation of Korea funded by the Ministry of Science & ICT (CISS-2012M3A6A054204, NRF-2017M3A9E2062685, 2018M3C1B8016147).
Publisher Copyright:
© 2018 Biophysical Society