Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Fotowat, Haleh, Engert, Florian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2023
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
_version_ 1784906919351156736
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
work_keys_str_mv AT fotowathaleh neuralcircuitsunderlyinghabituationofvisuallyevokedescapebehaviorsinlarvalzebrafish
AT engertflorian neuralcircuitsunderlyinghabituationofvisuallyevokedescapebehaviorsinlarvalzebrafish