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Optical mapping of neuronal activity during seizures in zebrafish
Mapping neuronal activity during the onset and propagation of epileptic seizures can provide a better understanding of the mechanisms underlying this pathology and improve our approaches to the development of new drugs. Recently, zebrafish has become an important model for studying epilepsy both in...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5465210/ https://www.ncbi.nlm.nih.gov/pubmed/28596596 http://dx.doi.org/10.1038/s41598-017-03087-z |
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author | Turrini, L. Fornetto, C. Marchetto, G. Müllenbroich, M. C. Tiso, N. Vettori, A. Resta, F. Masi, A. Mannaioni, G. Pavone, F. S. Vanzi, F. |
author_facet | Turrini, L. Fornetto, C. Marchetto, G. Müllenbroich, M. C. Tiso, N. Vettori, A. Resta, F. Masi, A. Mannaioni, G. Pavone, F. S. Vanzi, F. |
author_sort | Turrini, L. |
collection | PubMed |
description | Mapping neuronal activity during the onset and propagation of epileptic seizures can provide a better understanding of the mechanisms underlying this pathology and improve our approaches to the development of new drugs. Recently, zebrafish has become an important model for studying epilepsy both in basic research and in drug discovery. Here, we employed a transgenic line with pan-neuronal expression of the genetically-encoded calcium indicator GCaMP6s to measure neuronal activity in zebrafish larvae during seizures induced by pentylenetretrazole (PTZ). With this approach, we mapped neuronal activity in different areas of the larval brain, demonstrating the high sensitivity of this method to different levels of alteration, as induced by increasing PTZ concentrations, and the rescuing effect of an anti-epileptic drug. We also present simultaneous measurements of brain and locomotor activity, as well as a high-throughput assay, demonstrating that GCaMP measurements can complement behavioural assays for the detection of subclinical epileptic seizures, thus enabling future investigations on human hypomorphic mutations and more effective drug screening methods. Notably, the methodology described here can be easily applied to the study of many human neuropathologies modelled in zebrafish, allowing a simple and yet detailed investigation of brain activity alterations associated with the pathological phenotype. |
format | Online Article Text |
id | pubmed-5465210 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54652102017-06-14 Optical mapping of neuronal activity during seizures in zebrafish Turrini, L. Fornetto, C. Marchetto, G. Müllenbroich, M. C. Tiso, N. Vettori, A. Resta, F. Masi, A. Mannaioni, G. Pavone, F. S. Vanzi, F. Sci Rep Article Mapping neuronal activity during the onset and propagation of epileptic seizures can provide a better understanding of the mechanisms underlying this pathology and improve our approaches to the development of new drugs. Recently, zebrafish has become an important model for studying epilepsy both in basic research and in drug discovery. Here, we employed a transgenic line with pan-neuronal expression of the genetically-encoded calcium indicator GCaMP6s to measure neuronal activity in zebrafish larvae during seizures induced by pentylenetretrazole (PTZ). With this approach, we mapped neuronal activity in different areas of the larval brain, demonstrating the high sensitivity of this method to different levels of alteration, as induced by increasing PTZ concentrations, and the rescuing effect of an anti-epileptic drug. We also present simultaneous measurements of brain and locomotor activity, as well as a high-throughput assay, demonstrating that GCaMP measurements can complement behavioural assays for the detection of subclinical epileptic seizures, thus enabling future investigations on human hypomorphic mutations and more effective drug screening methods. Notably, the methodology described here can be easily applied to the study of many human neuropathologies modelled in zebrafish, allowing a simple and yet detailed investigation of brain activity alterations associated with the pathological phenotype. Nature Publishing Group UK 2017-06-08 /pmc/articles/PMC5465210/ /pubmed/28596596 http://dx.doi.org/10.1038/s41598-017-03087-z Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Turrini, L. Fornetto, C. Marchetto, G. Müllenbroich, M. C. Tiso, N. Vettori, A. Resta, F. Masi, A. Mannaioni, G. Pavone, F. S. Vanzi, F. Optical mapping of neuronal activity during seizures in zebrafish |
title | Optical mapping of neuronal activity during seizures in zebrafish |
title_full | Optical mapping of neuronal activity during seizures in zebrafish |
title_fullStr | Optical mapping of neuronal activity during seizures in zebrafish |
title_full_unstemmed | Optical mapping of neuronal activity during seizures in zebrafish |
title_short | Optical mapping of neuronal activity during seizures in zebrafish |
title_sort | optical mapping of neuronal activity during seizures in zebrafish |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5465210/ https://www.ncbi.nlm.nih.gov/pubmed/28596596 http://dx.doi.org/10.1038/s41598-017-03087-z |
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