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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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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. |
format | Online Article Text |
id | pubmed-8219385 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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