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Uncovering a ‘sensitive window’ of multisensory and motor neuroplasticity in the cerebrum and cerebellum of male and female starlings

Traditionally, research unraveling seasonal neuroplasticity in songbirds has focused on the male song control system and testosterone. We longitudinally monitored the song behavior and neuroplasticity in male and female starlings during multiple photoperiods using Diffusion Tensor and Fixel-Based te...

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Autores principales: Orije, Jasmien, Cardon, Emilie, Hamaide, Julie, Jonckers, Elisabeth, Darras, Veerle M, Verhoye, Marleen, Van der Linden, Annemie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8219385/
https://www.ncbi.nlm.nih.gov/pubmed/34096502
http://dx.doi.org/10.7554/eLife.66777
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author Orije, Jasmien
Cardon, Emilie
Hamaide, Julie
Jonckers, Elisabeth
Darras, Veerle M
Verhoye, Marleen
Van der Linden, Annemie
author_facet Orije, Jasmien
Cardon, Emilie
Hamaide, Julie
Jonckers, Elisabeth
Darras, Veerle M
Verhoye, Marleen
Van der Linden, Annemie
author_sort Orije, Jasmien
collection PubMed
description Traditionally, research unraveling seasonal neuroplasticity in songbirds has focused on the male song control system and testosterone. We longitudinally monitored the song behavior and neuroplasticity in male and female starlings during multiple photoperiods using Diffusion Tensor and Fixel-Based techniques. These exploratory data-driven whole-brain methods resulted in a population-based tractogram confirming microstructural sexual dimorphisms in the song control system. Furthermore, male brains showed hemispheric asymmetries in the pallium, whereas females had higher interhemispheric connectivity, which could not be attributed to brain size differences. Only females with large brains sing but differ from males in their song behavior by showing involvement of the hippocampus. Both sexes experienced multisensory neuroplasticity in the song control, auditory and visual system, and cerebellum, mainly during the photosensitive period. This period with low gonadal hormone levels might represent a ‘sensitive window’ during which different sensory and motor systems in the cerebrum and cerebellum can be seasonally re-shaped in both sexes.
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spelling pubmed-82193852021-06-23 Uncovering a ‘sensitive window’ of multisensory and motor neuroplasticity in the cerebrum and cerebellum of male and female starlings Orije, Jasmien Cardon, Emilie Hamaide, Julie Jonckers, Elisabeth Darras, Veerle M Verhoye, Marleen Van der Linden, Annemie eLife Neuroscience Traditionally, research unraveling seasonal neuroplasticity in songbirds has focused on the male song control system and testosterone. We longitudinally monitored the song behavior and neuroplasticity in male and female starlings during multiple photoperiods using Diffusion Tensor and Fixel-Based techniques. These exploratory data-driven whole-brain methods resulted in a population-based tractogram confirming microstructural sexual dimorphisms in the song control system. Furthermore, male brains showed hemispheric asymmetries in the pallium, whereas females had higher interhemispheric connectivity, which could not be attributed to brain size differences. Only females with large brains sing but differ from males in their song behavior by showing involvement of the hippocampus. Both sexes experienced multisensory neuroplasticity in the song control, auditory and visual system, and cerebellum, mainly during the photosensitive period. This period with low gonadal hormone levels might represent a ‘sensitive window’ during which different sensory and motor systems in the cerebrum and cerebellum can be seasonally re-shaped in both sexes. eLife Sciences Publications, Ltd 2021-06-07 /pmc/articles/PMC8219385/ /pubmed/34096502 http://dx.doi.org/10.7554/eLife.66777 Text en © 2021, Orije et al 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
Orije, Jasmien
Cardon, Emilie
Hamaide, Julie
Jonckers, Elisabeth
Darras, Veerle M
Verhoye, Marleen
Van der Linden, Annemie
Uncovering a ‘sensitive window’ of multisensory and motor neuroplasticity in the cerebrum and cerebellum of male and female starlings
title Uncovering a ‘sensitive window’ of multisensory and motor neuroplasticity in the cerebrum and cerebellum of male and female starlings
title_full Uncovering a ‘sensitive window’ of multisensory and motor neuroplasticity in the cerebrum and cerebellum of male and female starlings
title_fullStr Uncovering a ‘sensitive window’ of multisensory and motor neuroplasticity in the cerebrum and cerebellum of male and female starlings
title_full_unstemmed Uncovering a ‘sensitive window’ of multisensory and motor neuroplasticity in the cerebrum and cerebellum of male and female starlings
title_short Uncovering a ‘sensitive window’ of multisensory and motor neuroplasticity in the cerebrum and cerebellum of male and female starlings
title_sort uncovering a ‘sensitive window’ of multisensory and motor neuroplasticity in the cerebrum and cerebellum of male and female starlings
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8219385/
https://www.ncbi.nlm.nih.gov/pubmed/34096502
http://dx.doi.org/10.7554/eLife.66777
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