Cargando…

4-dimensional functional profiling in the convulsant-treated larval zebrafish brain

Functional neuroimaging, using genetically-encoded Ca(2+) sensors in larval zebrafish, offers a powerful combination of high spatiotemporal resolution and higher vertebrate relevance for quantitative neuropharmacological profiling. Here we use zebrafish larvae with pan-neuronal expression of GCaMP6s...

Descripción completa

Detalles Bibliográficos
Autores principales: Winter, Matthew J., Windell, Dylan, Metz, Jeremy, Matthews, Peter, Pinion, Joe, Brown, Jonathan T., Hetheridge, Malcolm J., Ball, Jonathan S., Owen, Stewart F., Redfern, Will S., Moger, Julian, Randall, Andrew D., Tyler, Charles R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5529444/
https://www.ncbi.nlm.nih.gov/pubmed/28747660
http://dx.doi.org/10.1038/s41598-017-06646-6
_version_ 1783253123442147328
author Winter, Matthew J.
Windell, Dylan
Metz, Jeremy
Matthews, Peter
Pinion, Joe
Brown, Jonathan T.
Hetheridge, Malcolm J.
Ball, Jonathan S.
Owen, Stewart F.
Redfern, Will S.
Moger, Julian
Randall, Andrew D.
Tyler, Charles R.
author_facet Winter, Matthew J.
Windell, Dylan
Metz, Jeremy
Matthews, Peter
Pinion, Joe
Brown, Jonathan T.
Hetheridge, Malcolm J.
Ball, Jonathan S.
Owen, Stewart F.
Redfern, Will S.
Moger, Julian
Randall, Andrew D.
Tyler, Charles R.
author_sort Winter, Matthew J.
collection PubMed
description Functional neuroimaging, using genetically-encoded Ca(2+) sensors in larval zebrafish, offers a powerful combination of high spatiotemporal resolution and higher vertebrate relevance for quantitative neuropharmacological profiling. Here we use zebrafish larvae with pan-neuronal expression of GCaMP6s, combined with light sheet microscopy and a novel image processing pipeline, for the 4D profiling of chemoconvulsant action in multiple brain regions. In untreated larvae, regions associated with autonomic functionality, sensory processing and stress-responsiveness, consistently exhibited elevated spontaneous activity. The application of drugs targeting different convulsant mechanisms (4-Aminopyridine, Pentylenetetrazole, Pilocarpine and Strychnine) resulted in distinct spatiotemporal patterns of activity. These activity patterns showed some interesting parallels with what is known of the distribution of their respective molecular targets, but crucially also revealed system-wide neural circuit responses to stimulation or suppression. Drug concentration-response curves of neural activity were identified in a number of anatomically-defined zebrafish brain regions, and in vivo larval electrophysiology, also conducted in 4dpf larvae, provided additional measures of neural activity. Our quantification of network-wide chemoconvulsant drug activity in the whole zebrafish brain illustrates the power of this approach for neuropharmacological profiling in applications ranging from accelerating studies of drug safety and efficacy, to identifying pharmacologically-altered networks in zebrafish models of human neurological disorders.
format Online
Article
Text
id pubmed-5529444
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-55294442017-08-02 4-dimensional functional profiling in the convulsant-treated larval zebrafish brain Winter, Matthew J. Windell, Dylan Metz, Jeremy Matthews, Peter Pinion, Joe Brown, Jonathan T. Hetheridge, Malcolm J. Ball, Jonathan S. Owen, Stewart F. Redfern, Will S. Moger, Julian Randall, Andrew D. Tyler, Charles R. Sci Rep Article Functional neuroimaging, using genetically-encoded Ca(2+) sensors in larval zebrafish, offers a powerful combination of high spatiotemporal resolution and higher vertebrate relevance for quantitative neuropharmacological profiling. Here we use zebrafish larvae with pan-neuronal expression of GCaMP6s, combined with light sheet microscopy and a novel image processing pipeline, for the 4D profiling of chemoconvulsant action in multiple brain regions. In untreated larvae, regions associated with autonomic functionality, sensory processing and stress-responsiveness, consistently exhibited elevated spontaneous activity. The application of drugs targeting different convulsant mechanisms (4-Aminopyridine, Pentylenetetrazole, Pilocarpine and Strychnine) resulted in distinct spatiotemporal patterns of activity. These activity patterns showed some interesting parallels with what is known of the distribution of their respective molecular targets, but crucially also revealed system-wide neural circuit responses to stimulation or suppression. Drug concentration-response curves of neural activity were identified in a number of anatomically-defined zebrafish brain regions, and in vivo larval electrophysiology, also conducted in 4dpf larvae, provided additional measures of neural activity. Our quantification of network-wide chemoconvulsant drug activity in the whole zebrafish brain illustrates the power of this approach for neuropharmacological profiling in applications ranging from accelerating studies of drug safety and efficacy, to identifying pharmacologically-altered networks in zebrafish models of human neurological disorders. Nature Publishing Group UK 2017-07-26 /pmc/articles/PMC5529444/ /pubmed/28747660 http://dx.doi.org/10.1038/s41598-017-06646-6 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
Winter, Matthew J.
Windell, Dylan
Metz, Jeremy
Matthews, Peter
Pinion, Joe
Brown, Jonathan T.
Hetheridge, Malcolm J.
Ball, Jonathan S.
Owen, Stewart F.
Redfern, Will S.
Moger, Julian
Randall, Andrew D.
Tyler, Charles R.
4-dimensional functional profiling in the convulsant-treated larval zebrafish brain
title 4-dimensional functional profiling in the convulsant-treated larval zebrafish brain
title_full 4-dimensional functional profiling in the convulsant-treated larval zebrafish brain
title_fullStr 4-dimensional functional profiling in the convulsant-treated larval zebrafish brain
title_full_unstemmed 4-dimensional functional profiling in the convulsant-treated larval zebrafish brain
title_short 4-dimensional functional profiling in the convulsant-treated larval zebrafish brain
title_sort 4-dimensional functional profiling in the convulsant-treated larval zebrafish brain
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5529444/
https://www.ncbi.nlm.nih.gov/pubmed/28747660
http://dx.doi.org/10.1038/s41598-017-06646-6
work_keys_str_mv AT wintermatthewj 4dimensionalfunctionalprofilingintheconvulsanttreatedlarvalzebrafishbrain
AT windelldylan 4dimensionalfunctionalprofilingintheconvulsanttreatedlarvalzebrafishbrain
AT metzjeremy 4dimensionalfunctionalprofilingintheconvulsanttreatedlarvalzebrafishbrain
AT matthewspeter 4dimensionalfunctionalprofilingintheconvulsanttreatedlarvalzebrafishbrain
AT pinionjoe 4dimensionalfunctionalprofilingintheconvulsanttreatedlarvalzebrafishbrain
AT brownjonathant 4dimensionalfunctionalprofilingintheconvulsanttreatedlarvalzebrafishbrain
AT hetheridgemalcolmj 4dimensionalfunctionalprofilingintheconvulsanttreatedlarvalzebrafishbrain
AT balljonathans 4dimensionalfunctionalprofilingintheconvulsanttreatedlarvalzebrafishbrain
AT owenstewartf 4dimensionalfunctionalprofilingintheconvulsanttreatedlarvalzebrafishbrain
AT redfernwills 4dimensionalfunctionalprofilingintheconvulsanttreatedlarvalzebrafishbrain
AT mogerjulian 4dimensionalfunctionalprofilingintheconvulsanttreatedlarvalzebrafishbrain
AT randallandrewd 4dimensionalfunctionalprofilingintheconvulsanttreatedlarvalzebrafishbrain
AT tylercharlesr 4dimensionalfunctionalprofilingintheconvulsanttreatedlarvalzebrafishbrain