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Regulation of mouse exploratory behaviour by irradiance and cone-opponent signals

BACKGROUND: Animal survival depends on the ability to adjust behaviour according to environmental conditions. The circadian system plays a key role in this capability, with diel changes in the quantity (irradiance) and spectral content (‘colour’) of ambient illumination providing signals of time-of-...

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Autores principales: Tamayo, E., Mouland, J. W., Lucas, R. J., Brown, T. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10441731/
https://www.ncbi.nlm.nih.gov/pubmed/37605163
http://dx.doi.org/10.1186/s12915-023-01663-6
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author Tamayo, E.
Mouland, J. W.
Lucas, R. J.
Brown, T. M.
author_facet Tamayo, E.
Mouland, J. W.
Lucas, R. J.
Brown, T. M.
author_sort Tamayo, E.
collection PubMed
description BACKGROUND: Animal survival depends on the ability to adjust behaviour according to environmental conditions. The circadian system plays a key role in this capability, with diel changes in the quantity (irradiance) and spectral content (‘colour’) of ambient illumination providing signals of time-of-day that regulate the timing of rest and activity. Light also exerts much more immediate effects on behaviour, however, that are equally important in shaping daily activity patterns. Hence, nocturnal mammals will actively avoid light and dramatically reduce their activity when light cannot be avoided. The sensory mechanisms underlying these acute effects of light are incompletely understood, particularly the importance of colour. RESULTS: To define sensory mechanisms controlling mouse behaviour, we used photoreceptor-isolating stimuli and mice with altered cone spectral sensitivity (Opn1mwR), lacking melanopsin (Opn1mwR; Opn4(−/−)) or cone phototransduction (Cnga3(−/−)) in assays of light-avoidance and activity suppression. In addition to roles for melanopsin-dependent irradiance signals, we find a major influence of spectral content in both cases. Hence, remarkably, selective increases in S-cone irradiance (producing a blue-shift in spectrum replicating twilight) drive light-seeking behaviour and promote activity. These effects are opposed by signals from longer-wavelength sensitive cones, indicating a true spectrally-opponent mechanism. Using c-Fos-mapping and multielectrode electrophysiology, we further show these effects are associated with a selective cone-opponent modulation of neural activity in the key brain site implicated in acute effects of light on behaviour, the subparaventricular zone. CONCLUSIONS: Collectively, these data reveal a mechanism whereby blue-shifts in the spectrum of environmental illumination, such as during twilight, promote mouse exploratory behaviour. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-023-01663-6.
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spelling pubmed-104417312023-08-22 Regulation of mouse exploratory behaviour by irradiance and cone-opponent signals Tamayo, E. Mouland, J. W. Lucas, R. J. Brown, T. M. BMC Biol Research Article BACKGROUND: Animal survival depends on the ability to adjust behaviour according to environmental conditions. The circadian system plays a key role in this capability, with diel changes in the quantity (irradiance) and spectral content (‘colour’) of ambient illumination providing signals of time-of-day that regulate the timing of rest and activity. Light also exerts much more immediate effects on behaviour, however, that are equally important in shaping daily activity patterns. Hence, nocturnal mammals will actively avoid light and dramatically reduce their activity when light cannot be avoided. The sensory mechanisms underlying these acute effects of light are incompletely understood, particularly the importance of colour. RESULTS: To define sensory mechanisms controlling mouse behaviour, we used photoreceptor-isolating stimuli and mice with altered cone spectral sensitivity (Opn1mwR), lacking melanopsin (Opn1mwR; Opn4(−/−)) or cone phototransduction (Cnga3(−/−)) in assays of light-avoidance and activity suppression. In addition to roles for melanopsin-dependent irradiance signals, we find a major influence of spectral content in both cases. Hence, remarkably, selective increases in S-cone irradiance (producing a blue-shift in spectrum replicating twilight) drive light-seeking behaviour and promote activity. These effects are opposed by signals from longer-wavelength sensitive cones, indicating a true spectrally-opponent mechanism. Using c-Fos-mapping and multielectrode electrophysiology, we further show these effects are associated with a selective cone-opponent modulation of neural activity in the key brain site implicated in acute effects of light on behaviour, the subparaventricular zone. CONCLUSIONS: Collectively, these data reveal a mechanism whereby blue-shifts in the spectrum of environmental illumination, such as during twilight, promote mouse exploratory behaviour. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-023-01663-6. BioMed Central 2023-08-21 /pmc/articles/PMC10441731/ /pubmed/37605163 http://dx.doi.org/10.1186/s12915-023-01663-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Tamayo, E.
Mouland, J. W.
Lucas, R. J.
Brown, T. M.
Regulation of mouse exploratory behaviour by irradiance and cone-opponent signals
title Regulation of mouse exploratory behaviour by irradiance and cone-opponent signals
title_full Regulation of mouse exploratory behaviour by irradiance and cone-opponent signals
title_fullStr Regulation of mouse exploratory behaviour by irradiance and cone-opponent signals
title_full_unstemmed Regulation of mouse exploratory behaviour by irradiance and cone-opponent signals
title_short Regulation of mouse exploratory behaviour by irradiance and cone-opponent signals
title_sort regulation of mouse exploratory behaviour by irradiance and cone-opponent signals
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10441731/
https://www.ncbi.nlm.nih.gov/pubmed/37605163
http://dx.doi.org/10.1186/s12915-023-01663-6
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