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A brain for all seasons: An in vivo MRI perspective on songbirds

Seasonality in songbirds includes not only reproduction but also seasonal changes in singing behavior and its neural substrate, the song control system (SCS). Prior research mainly focused on the role of sex steroids on this seasonal SCS neuroplasticity in males. In this review, we summarize the adv...

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Autores principales: Orije, Jasmien Ellen Maria Jozef, Van der Linden, Annemie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804379/
https://www.ncbi.nlm.nih.gov/pubmed/35989548
http://dx.doi.org/10.1002/jez.2650
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author Orije, Jasmien Ellen Maria Jozef
Van der Linden, Annemie
author_facet Orije, Jasmien Ellen Maria Jozef
Van der Linden, Annemie
author_sort Orije, Jasmien Ellen Maria Jozef
collection PubMed
description Seasonality in songbirds includes not only reproduction but also seasonal changes in singing behavior and its neural substrate, the song control system (SCS). Prior research mainly focused on the role of sex steroids on this seasonal SCS neuroplasticity in males. In this review, we summarize the advances made in the field of seasonal neuroplasticity by applying in vivo magnetic resonance imaging (MRI) in male and female starlings, analyzing the entire brain, monitoring birds longitudinally and determining the neuronal correlates of seasonal variations in plasma hormone levels and song behavior. The first MRI studies in songbirds used manganese enhanced MRI to visualize the SCS in a living bird and validated previously described brain volume changes related to different seasons and testosterone. MRI studies with testosterone implantation established how the consequential boost in singing was correlated to structural changes in the SCS, indicating activity‐induced neuroplasticity as song proficiency increased. Next, diffusion tensor MRI explored seasonal neuroplasticity in the entire brain, focusing on networks beyond the SCS, revealing that other sensory systems and even the cerebellum, which is important for the integration of sensory perception and song behavior, experience neuroplasticity starting in the photosensitive period. Functional MRI showed that olfactory, and auditory processing was modulated by the seasons. The convergence of seasonal variations in so many sensory and sensorimotor systems resembles multisensory neuroplasticity during the critical period early in life. This sheds new light on seasonal songbirds as a model for unlocking the brain by recreating seasonally the permissive circumstances for heightened neuroplasticity.
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spelling pubmed-98043792023-01-03 A brain for all seasons: An in vivo MRI perspective on songbirds Orije, Jasmien Ellen Maria Jozef Van der Linden, Annemie J Exp Zool A Ecol Integr Physiol Reviews Seasonality in songbirds includes not only reproduction but also seasonal changes in singing behavior and its neural substrate, the song control system (SCS). Prior research mainly focused on the role of sex steroids on this seasonal SCS neuroplasticity in males. In this review, we summarize the advances made in the field of seasonal neuroplasticity by applying in vivo magnetic resonance imaging (MRI) in male and female starlings, analyzing the entire brain, monitoring birds longitudinally and determining the neuronal correlates of seasonal variations in plasma hormone levels and song behavior. The first MRI studies in songbirds used manganese enhanced MRI to visualize the SCS in a living bird and validated previously described brain volume changes related to different seasons and testosterone. MRI studies with testosterone implantation established how the consequential boost in singing was correlated to structural changes in the SCS, indicating activity‐induced neuroplasticity as song proficiency increased. Next, diffusion tensor MRI explored seasonal neuroplasticity in the entire brain, focusing on networks beyond the SCS, revealing that other sensory systems and even the cerebellum, which is important for the integration of sensory perception and song behavior, experience neuroplasticity starting in the photosensitive period. Functional MRI showed that olfactory, and auditory processing was modulated by the seasons. The convergence of seasonal variations in so many sensory and sensorimotor systems resembles multisensory neuroplasticity during the critical period early in life. This sheds new light on seasonal songbirds as a model for unlocking the brain by recreating seasonally the permissive circumstances for heightened neuroplasticity. John Wiley and Sons Inc. 2022-08-21 2022-12-01 /pmc/articles/PMC9804379/ /pubmed/35989548 http://dx.doi.org/10.1002/jez.2650 Text en © 2022 The Authors. Journal of Experimental Zoology Part A: Ecological Genetics and Physiology published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Reviews
Orije, Jasmien Ellen Maria Jozef
Van der Linden, Annemie
A brain for all seasons: An in vivo MRI perspective on songbirds
title A brain for all seasons: An in vivo MRI perspective on songbirds
title_full A brain for all seasons: An in vivo MRI perspective on songbirds
title_fullStr A brain for all seasons: An in vivo MRI perspective on songbirds
title_full_unstemmed A brain for all seasons: An in vivo MRI perspective on songbirds
title_short A brain for all seasons: An in vivo MRI perspective on songbirds
title_sort brain for all seasons: an in vivo mri perspective on songbirds
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804379/
https://www.ncbi.nlm.nih.gov/pubmed/35989548
http://dx.doi.org/10.1002/jez.2650
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