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Two-Photon Imaging with Diffractive Optical Elements

Two-photon imaging has become a useful tool for optical monitoring of neural circuits, but it requires high laser power and serial scanning of each pixel in a sample. This results in slow imaging rates, limiting the measurements of fast signals such as neuronal activity. To improve the speed and sig...

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Detalles Bibliográficos
Autores principales: Watson, Brendon O., Nikolenko, Volodymyr, Yuste, Rafael
Formato: Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2715267/
https://www.ncbi.nlm.nih.gov/pubmed/19636390
http://dx.doi.org/10.3389/neuro.04.006.2009
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author Watson, Brendon O.
Nikolenko, Volodymyr
Yuste, Rafael
author_facet Watson, Brendon O.
Nikolenko, Volodymyr
Yuste, Rafael
author_sort Watson, Brendon O.
collection PubMed
description Two-photon imaging has become a useful tool for optical monitoring of neural circuits, but it requires high laser power and serial scanning of each pixel in a sample. This results in slow imaging rates, limiting the measurements of fast signals such as neuronal activity. To improve the speed and signal-to-noise ratio of two-photon imaging, we introduce a simple modification of a two-photon microscope, using a diffractive optical element (DOE) which splits the laser beam into several beamlets that can simultaneously scan the sample. We demonstrate the advantages of DOE scanning by enhancing the speed and sensitivity of two-photon calcium imaging of action potentials in neurons from neocortical brain slices. DOE scanning can easily improve the detection of time-varying signals in two-photon and other non-linear microscopic techniques.
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spelling pubmed-27152672009-07-27 Two-Photon Imaging with Diffractive Optical Elements Watson, Brendon O. Nikolenko, Volodymyr Yuste, Rafael Front Neural Circuits Neuroscience Two-photon imaging has become a useful tool for optical monitoring of neural circuits, but it requires high laser power and serial scanning of each pixel in a sample. This results in slow imaging rates, limiting the measurements of fast signals such as neuronal activity. To improve the speed and signal-to-noise ratio of two-photon imaging, we introduce a simple modification of a two-photon microscope, using a diffractive optical element (DOE) which splits the laser beam into several beamlets that can simultaneously scan the sample. We demonstrate the advantages of DOE scanning by enhancing the speed and sensitivity of two-photon calcium imaging of action potentials in neurons from neocortical brain slices. DOE scanning can easily improve the detection of time-varying signals in two-photon and other non-linear microscopic techniques. Frontiers Research Foundation 2009-07-06 /pmc/articles/PMC2715267/ /pubmed/19636390 http://dx.doi.org/10.3389/neuro.04.006.2009 Text en Copyright © 2009 Watson, Nikolenko and Yuste. http://www.frontiersin.org/licenseagreement This is an open-access article subject to an exclusive license agreement between the authors and the Frontiers Research Foundation, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited.
spellingShingle Neuroscience
Watson, Brendon O.
Nikolenko, Volodymyr
Yuste, Rafael
Two-Photon Imaging with Diffractive Optical Elements
title Two-Photon Imaging with Diffractive Optical Elements
title_full Two-Photon Imaging with Diffractive Optical Elements
title_fullStr Two-Photon Imaging with Diffractive Optical Elements
title_full_unstemmed Two-Photon Imaging with Diffractive Optical Elements
title_short Two-Photon Imaging with Diffractive Optical Elements
title_sort two-photon imaging with diffractive optical elements
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2715267/
https://www.ncbi.nlm.nih.gov/pubmed/19636390
http://dx.doi.org/10.3389/neuro.04.006.2009
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