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Photorelease of GABA with Visible Light Using an Inorganic Caging Group

We describe the selective photorelease of γ-amino butyric acid (GABA) with a novel caged-GABA compound that uses a ruthenium complex as photosensor. This compound (“RuBi-GABA”) can be excited with visible wavelengths, providing greater tissue penetration, less photo-toxicity, and faster photorelease...

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Detalles Bibliográficos
Autores principales: Rial Verde, Emiliano M., Zayat, Leonardo, Etchenique, Roberto, Yuste, Rafael
Formato: Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2567106/
https://www.ncbi.nlm.nih.gov/pubmed/18946542
http://dx.doi.org/10.3389/neuro.04.002.2008
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author Rial Verde, Emiliano M.
Zayat, Leonardo
Etchenique, Roberto
Yuste, Rafael
author_facet Rial Verde, Emiliano M.
Zayat, Leonardo
Etchenique, Roberto
Yuste, Rafael
author_sort Rial Verde, Emiliano M.
collection PubMed
description We describe the selective photorelease of γ-amino butyric acid (GABA) with a novel caged-GABA compound that uses a ruthenium complex as photosensor. This compound (“RuBi-GABA”) can be excited with visible wavelengths, providing greater tissue penetration, less photo-toxicity, and faster photorelease kinetics than currently used UV light-sensitive caged compounds. Using pyramidal neurons from neocortical brain slices, we show that RuBi-GABA uncaging induces GABA-A receptor-mediated responses, has no detectable side effects on endogenous GABAergic and glutamatergic receptors and generates responses with kinetics and spatial resolution comparable to the best caged GABA compounds presently available. Finally, we illustrate two potential applications of RuBi-GABA uncaging: GABA receptor mapping, and optical silencing of neuronal firing.
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spelling pubmed-25671062008-10-22 Photorelease of GABA with Visible Light Using an Inorganic Caging Group Rial Verde, Emiliano M. Zayat, Leonardo Etchenique, Roberto Yuste, Rafael Front Neural Circuits Neuroscience We describe the selective photorelease of γ-amino butyric acid (GABA) with a novel caged-GABA compound that uses a ruthenium complex as photosensor. This compound (“RuBi-GABA”) can be excited with visible wavelengths, providing greater tissue penetration, less photo-toxicity, and faster photorelease kinetics than currently used UV light-sensitive caged compounds. Using pyramidal neurons from neocortical brain slices, we show that RuBi-GABA uncaging induces GABA-A receptor-mediated responses, has no detectable side effects on endogenous GABAergic and glutamatergic receptors and generates responses with kinetics and spatial resolution comparable to the best caged GABA compounds presently available. Finally, we illustrate two potential applications of RuBi-GABA uncaging: GABA receptor mapping, and optical silencing of neuronal firing. Frontiers Research Foundation 2008-08-13 /pmc/articles/PMC2567106/ /pubmed/18946542 http://dx.doi.org/10.3389/neuro.04.002.2008 Text en Copyright © 2008 Rial Verde, Zayat, Etchenique 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
Rial Verde, Emiliano M.
Zayat, Leonardo
Etchenique, Roberto
Yuste, Rafael
Photorelease of GABA with Visible Light Using an Inorganic Caging Group
title Photorelease of GABA with Visible Light Using an Inorganic Caging Group
title_full Photorelease of GABA with Visible Light Using an Inorganic Caging Group
title_fullStr Photorelease of GABA with Visible Light Using an Inorganic Caging Group
title_full_unstemmed Photorelease of GABA with Visible Light Using an Inorganic Caging Group
title_short Photorelease of GABA with Visible Light Using an Inorganic Caging Group
title_sort photorelease of gaba with visible light using an inorganic caging group
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2567106/
https://www.ncbi.nlm.nih.gov/pubmed/18946542
http://dx.doi.org/10.3389/neuro.04.002.2008
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