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Calcium imaging of infrared-stimulated activity in rodent brain.
Cayce, Jonathan Matthew; Bouchard, Matthew B; Chernov, Mykyta M; Chen, Brenda R; Grosberg, Lauren E; Jansen, E Duco; Hillman, Elizabeth M C; Mahadevan-Jansen, Anita.
Afiliación
  • Cayce JM; Department of Biomedical Engineering, Vanderbilt University, Station B, Box 351631, Nashville TN 37235, United States.
  • Bouchard MB; Laboratory for Functional Optical Imaging, Departments of Biomedical Engineering and Radiology, Columbia University, 120th Street and Amsterdam Avenue, New York, NY 10027, United States.
  • Chernov MM; Department of Biomedical Engineering, Vanderbilt University, Station B, Box 351631, Nashville TN 37235, United States.
  • Chen BR; Laboratory for Functional Optical Imaging, Departments of Biomedical Engineering and Radiology, Columbia University, 120th Street and Amsterdam Avenue, New York, NY 10027, United States.
  • Grosberg LE; Laboratory for Functional Optical Imaging, Departments of Biomedical Engineering and Radiology, Columbia University, 120th Street and Amsterdam Avenue, New York, NY 10027, United States.
  • Jansen ED; Department of Biomedical Engineering, Vanderbilt University, Station B, Box 351631, Nashville TN 37235, United States.
  • Hillman EM; Laboratory for Functional Optical Imaging, Departments of Biomedical Engineering and Radiology, Columbia University, 120th Street and Amsterdam Avenue, New York, NY 10027, United States.
  • Mahadevan-Jansen A; Department of Biomedical Engineering, Vanderbilt University, Station B, Box 351631, Nashville TN 37235, United States. Electronic address: anita.mahadevan-jansen@vanderbilt.edu.
Cell Calcium ; 55(4): 183-90, 2014 Apr.
Article en En | MEDLINE | ID: mdl-24674600
ABSTRACT
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.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Encéfalo / Calcio Límite: Animals Idioma: En Revista: Cell Calcium Año: 2014 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Encéfalo / Calcio Límite: Animals Idioma: En Revista: Cell Calcium Año: 2014 Tipo del documento: Article País de afiliación: Estados Unidos