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Sex-specific divergent maturational trajectories in the postnatal rat basolateral amygdala

In rodents and humans, the basolateral amygdala (BLA), essential for emotional behaviors, is profoundly reorganized during adolescence. We compared in both sexes the morphology, neuronal, and synaptic properties of BLA neurons in rats at puberty and adulthood. BLA neurons were more excitable in male...

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Detalles Bibliográficos
Autores principales: Guily, Pauline, Lassalle, Olivier, Chavis, Pascale, Manzoni, Olivier J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8841815/
https://www.ncbi.nlm.nih.gov/pubmed/35198880
http://dx.doi.org/10.1016/j.isci.2022.103815
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author Guily, Pauline
Lassalle, Olivier
Chavis, Pascale
Manzoni, Olivier J.
author_facet Guily, Pauline
Lassalle, Olivier
Chavis, Pascale
Manzoni, Olivier J.
author_sort Guily, Pauline
collection PubMed
description In rodents and humans, the basolateral amygdala (BLA), essential for emotional behaviors, is profoundly reorganized during adolescence. We compared in both sexes the morphology, neuronal, and synaptic properties of BLA neurons in rats at puberty and adulthood. BLA neurons were more excitable in males than in females at adulthood. At pubescence, male action potentials were smaller and shorter than females’ while fast afterhyperpolarizations were larger in males. During postnatal maturation, spine length increased and decreased in females and males, respectively, while there was a reduction in spine head size in females. Excitatory synaptic properties, estimated from stimuli-response relationships, spontaneous post-synaptic currents, and AMPA/NMDA ratio also displayed sex-specific maturational differences. Finally, the developmental courses of long-term potentiation and depression were sexually dimorphic. These data reveal divergent maturational trajectories in the BLA of male and female rats and suggest sex-specific substrates to the BLA linked behaviors at adolescence and adulthood.
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spelling pubmed-88418152022-02-22 Sex-specific divergent maturational trajectories in the postnatal rat basolateral amygdala Guily, Pauline Lassalle, Olivier Chavis, Pascale Manzoni, Olivier J. iScience Article In rodents and humans, the basolateral amygdala (BLA), essential for emotional behaviors, is profoundly reorganized during adolescence. We compared in both sexes the morphology, neuronal, and synaptic properties of BLA neurons in rats at puberty and adulthood. BLA neurons were more excitable in males than in females at adulthood. At pubescence, male action potentials were smaller and shorter than females’ while fast afterhyperpolarizations were larger in males. During postnatal maturation, spine length increased and decreased in females and males, respectively, while there was a reduction in spine head size in females. Excitatory synaptic properties, estimated from stimuli-response relationships, spontaneous post-synaptic currents, and AMPA/NMDA ratio also displayed sex-specific maturational differences. Finally, the developmental courses of long-term potentiation and depression were sexually dimorphic. These data reveal divergent maturational trajectories in the BLA of male and female rats and suggest sex-specific substrates to the BLA linked behaviors at adolescence and adulthood. Elsevier 2022-01-25 /pmc/articles/PMC8841815/ /pubmed/35198880 http://dx.doi.org/10.1016/j.isci.2022.103815 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Guily, Pauline
Lassalle, Olivier
Chavis, Pascale
Manzoni, Olivier J.
Sex-specific divergent maturational trajectories in the postnatal rat basolateral amygdala
title Sex-specific divergent maturational trajectories in the postnatal rat basolateral amygdala
title_full Sex-specific divergent maturational trajectories in the postnatal rat basolateral amygdala
title_fullStr Sex-specific divergent maturational trajectories in the postnatal rat basolateral amygdala
title_full_unstemmed Sex-specific divergent maturational trajectories in the postnatal rat basolateral amygdala
title_short Sex-specific divergent maturational trajectories in the postnatal rat basolateral amygdala
title_sort sex-specific divergent maturational trajectories in the postnatal rat basolateral amygdala
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8841815/
https://www.ncbi.nlm.nih.gov/pubmed/35198880
http://dx.doi.org/10.1016/j.isci.2022.103815
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