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Calcium imaging of infrared-stimulated activity in rodent brain

Identifieur interne : 000327 ( Pmc/Corpus ); précédent : 000326; suivant : 000328

Calcium imaging of infrared-stimulated activity in rodent brain

Auteurs : Jonathan Matthew Cayce ; Matthew B. Bouchard ; Mykyta M. Chernov ; Brenda R. Chen ; Lauren E. Grosberg ; E. Duco Jansen ; Elizabeth M. C. Hillman ; Anita Mahadevan-Jansen

Source :

RBID : PMC:4014070

Abstract

Summary

Infrared neural stimulation (INS) is a promising neurostimulation technique that can activate neural tissue with high spatial precision and without the need for exogenous agents. However, little is understood about how infrared light interacts with neural tissue on a cellular level, particularly within the living brain. In this study, we use calcium sensitive dye imaging on macroscopic and microscopic scales to explore the spatiotemporal effects of INS on cortical calcium dynamics. The INS-evoked calcium signal that was observed exhibited a fast and slow component suggesting activation of multiple cellular mechanisms. The slow component of the evoked signal exhibited wave-like properties suggesting network activation, and was verified to originate from astrocytes through pharmacology and 2-photon imaging. We also provide evidence that the fast calcium signal may have been evoked through modulation of glutamate transients. This study demonstrates that pulsed infrared light can induce intracellular calcium modulations in both astrocytes and neurons, providing new insights into the mechanisms of action of INS in the brain.


Url:
DOI: 10.1016/j.ceca.2014.01.004
PubMed: 24674600
PubMed Central: 4014070

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PMC:4014070

Le document en format XML

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<title>Summary</title>
<p id="P3">Infrared neural stimulation (INS) is a promising neurostimulation technique that can activate neural tissue with high spatial precision and without the need for exogenous agents. However, little is understood about how infrared light interacts with neural tissue on a cellular level, particularly within the living brain. In this study, we use calcium sensitive dye imaging on macroscopic and microscopic scales to explore the spatiotemporal effects of INS on cortical calcium dynamics. The INS-evoked calcium signal that was observed exhibited a fast and slow component suggesting activation of multiple cellular mechanisms. The slow component of the evoked signal exhibited wave-like properties suggesting network activation, and was verified to originate from astrocytes through pharmacology and 2-photon imaging. We also provide evidence that the fast calcium signal may have been evoked through modulation of glutamate transients. This study demonstrates that pulsed infrared light can induce intracellular calcium modulations in both astrocytes and neurons, providing new insights into the mechanisms of action of INS in the brain.</p>
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<given-names>Jonathan Matthew</given-names>
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Department of Biomedical Engineering, Vanderbilt University, Station B, Box 351631, Nashville, TN 37235</aff>
<aff id="A2">
<label>2</label>
Laboratory for Functional Optical Imaging, Departments of Biomedical Engineering and Radiology, Columbia University, 120th Street and Amsterdam Ave New York, NY 10027</aff>
<author-notes>
<corresp id="FN1">Corresponding Author: Dr. Anita Mahadevan-Jansen, Station B, Box 351631, Nashville, TN 37235,
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, 615-343-4787</corresp>
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<copyright-statement>© 2014 Elsevier Ltd. All rights reserved.</copyright-statement>
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<abstract>
<title>Summary</title>
<p id="P3">Infrared neural stimulation (INS) is a promising neurostimulation technique that can activate neural tissue with high spatial precision and without the need for exogenous agents. However, little is understood about how infrared light interacts with neural tissue on a cellular level, particularly within the living brain. In this study, we use calcium sensitive dye imaging on macroscopic and microscopic scales to explore the spatiotemporal effects of INS on cortical calcium dynamics. The INS-evoked calcium signal that was observed exhibited a fast and slow component suggesting activation of multiple cellular mechanisms. The slow component of the evoked signal exhibited wave-like properties suggesting network activation, and was verified to originate from astrocytes through pharmacology and 2-photon imaging. We also provide evidence that the fast calcium signal may have been evoked through modulation of glutamate transients. This study demonstrates that pulsed infrared light can induce intracellular calcium modulations in both astrocytes and neurons, providing new insights into the mechanisms of action of INS in the brain.</p>
</abstract>
<kwd-group>
<kwd>infrared neural stimulation</kwd>
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<kwd>somatosensory cortex</kwd>
<kwd>optical imaging</kwd>
<kwd>calcium dye imaging</kwd>
<kwd>neurons</kwd>
<kwd>astrocytes</kwd>
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