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Neural circuits underlying habituation of visually evoked escape behaviors in larval zebrafish
Larval zebrafish that are exposed repeatedly to dark looming stimuli will quickly habituate to these aversive signals and cease to respond with their stereotypical escape swims. A dark looming stimulus can be separated into two independent components: one that is characterized by an overall spatial...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10014075/ https://www.ncbi.nlm.nih.gov/pubmed/36916795 http://dx.doi.org/10.7554/eLife.82916 |
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author | Fotowat, Haleh Engert, Florian |
author_facet | Fotowat, Haleh Engert, Florian |
author_sort | Fotowat, Haleh |
collection | PubMed |
description | Larval zebrafish that are exposed repeatedly to dark looming stimuli will quickly habituate to these aversive signals and cease to respond with their stereotypical escape swims. A dark looming stimulus can be separated into two independent components: one that is characterized by an overall spatial expansion, where overall luminance is maintained at the same level, and a second, that represents an overall dimming within the whole visual field in the absence of any motion energy. Using specific stimulation patterns that isolate these independent components, we first extracted the behavioral algorithms that dictate how these separate information channels interact with each other and across the two eyes during the habituation process. Concurrent brain wide imaging experiments then permitted the construction of circuit models that suggest the existence of two separate neural pathways. The first is a looming channel which responds specifically to expanding edges presented to the contralateral eye and relays that information to the brain stem escape network to generate directed escapes. The second is a dimming-specific channel that could be either monocular or binocularly responsive, and that appears to specifically inhibit escape response when activated. We propose that this second channel is under strong contextual modulation and that it is primarily responsible for the incremental silencing of successive dark looming-evoked escapes. |
format | Online Article Text |
id | pubmed-10014075 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-100140752023-03-15 Neural circuits underlying habituation of visually evoked escape behaviors in larval zebrafish Fotowat, Haleh Engert, Florian eLife Neuroscience Larval zebrafish that are exposed repeatedly to dark looming stimuli will quickly habituate to these aversive signals and cease to respond with their stereotypical escape swims. A dark looming stimulus can be separated into two independent components: one that is characterized by an overall spatial expansion, where overall luminance is maintained at the same level, and a second, that represents an overall dimming within the whole visual field in the absence of any motion energy. Using specific stimulation patterns that isolate these independent components, we first extracted the behavioral algorithms that dictate how these separate information channels interact with each other and across the two eyes during the habituation process. Concurrent brain wide imaging experiments then permitted the construction of circuit models that suggest the existence of two separate neural pathways. The first is a looming channel which responds specifically to expanding edges presented to the contralateral eye and relays that information to the brain stem escape network to generate directed escapes. The second is a dimming-specific channel that could be either monocular or binocularly responsive, and that appears to specifically inhibit escape response when activated. We propose that this second channel is under strong contextual modulation and that it is primarily responsible for the incremental silencing of successive dark looming-evoked escapes. eLife Sciences Publications, Ltd 2023-03-14 /pmc/articles/PMC10014075/ /pubmed/36916795 http://dx.doi.org/10.7554/eLife.82916 Text en © 2023, Fotowat and Engert https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Fotowat, Haleh Engert, Florian Neural circuits underlying habituation of visually evoked escape behaviors in larval zebrafish |
title | Neural circuits underlying habituation of visually evoked escape behaviors in larval zebrafish |
title_full | Neural circuits underlying habituation of visually evoked escape behaviors in larval zebrafish |
title_fullStr | Neural circuits underlying habituation of visually evoked escape behaviors in larval zebrafish |
title_full_unstemmed | Neural circuits underlying habituation of visually evoked escape behaviors in larval zebrafish |
title_short | Neural circuits underlying habituation of visually evoked escape behaviors in larval zebrafish |
title_sort | neural circuits underlying habituation of visually evoked escape behaviors in larval zebrafish |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10014075/ https://www.ncbi.nlm.nih.gov/pubmed/36916795 http://dx.doi.org/10.7554/eLife.82916 |
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