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Age‐dependent sexual dimorphism in hippocampal cornu ammonis‐1 perineuronal net expression in rats

INTRODUCTION: Perineuronal nets (PNNs) are extracellular matrices that encompass parvalbumin‐expressing parvalbumin positive (PVALB+) fast‐spiking inhibitory interneurons where they protect and stabilize afferent synapses. Recent observations that gonadal hormones influence PVALB+ neuron development...

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Autores principales: Griffiths, Brian B., Madden, Amanda M. K., Edwards, Kimbra A., Zup, Susan L., Stary, Creed M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6520292/
https://www.ncbi.nlm.nih.gov/pubmed/30912298
http://dx.doi.org/10.1002/brb3.1265
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author Griffiths, Brian B.
Madden, Amanda M. K.
Edwards, Kimbra A.
Zup, Susan L.
Stary, Creed M.
author_facet Griffiths, Brian B.
Madden, Amanda M. K.
Edwards, Kimbra A.
Zup, Susan L.
Stary, Creed M.
author_sort Griffiths, Brian B.
collection PubMed
description INTRODUCTION: Perineuronal nets (PNNs) are extracellular matrices that encompass parvalbumin‐expressing parvalbumin positive (PVALB+) fast‐spiking inhibitory interneurons where they protect and stabilize afferent synapses. Recent observations that gonadal hormones influence PVALB+ neuron development suggest that PNN regulation may be sexually dimorphic. Sex differences in PNN abundance and complexity have been reported in sexually dimorphic nuclei in zebra finch brains; however, corresponding differences in mammalian brains have not been investigated. METHODS: In this study we assessed the number of cortical and hippocampal PNNs in juvenile and young adult male and female rats using fluorescent immunohistochemistry for PVALB and the PNN marker Wisteria Floribunda Lectin. RESULTS: We report here that PNNs are numerous and well developed in hippocampal cornu ammonis‐1 of adult males but are lower in juvenile and possibly adult females. No significant differences were observed between sexes in cornu ammonis‐3 or adjacent neocortex. There was an observed developmental difference in the neocortex as juveniles had more PVALB+ cells, but fewer PNN+ cells, than adults. CONCLUSIONS: Because PNNs are integral for several hippocampal‐mediated learning and memory tasks, these observations have potential sex‐dependent translational implications for clinical strategies targeting cognitive dysfunction.
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spelling pubmed-65202922019-05-23 Age‐dependent sexual dimorphism in hippocampal cornu ammonis‐1 perineuronal net expression in rats Griffiths, Brian B. Madden, Amanda M. K. Edwards, Kimbra A. Zup, Susan L. Stary, Creed M. Brain Behav Original Research INTRODUCTION: Perineuronal nets (PNNs) are extracellular matrices that encompass parvalbumin‐expressing parvalbumin positive (PVALB+) fast‐spiking inhibitory interneurons where they protect and stabilize afferent synapses. Recent observations that gonadal hormones influence PVALB+ neuron development suggest that PNN regulation may be sexually dimorphic. Sex differences in PNN abundance and complexity have been reported in sexually dimorphic nuclei in zebra finch brains; however, corresponding differences in mammalian brains have not been investigated. METHODS: In this study we assessed the number of cortical and hippocampal PNNs in juvenile and young adult male and female rats using fluorescent immunohistochemistry for PVALB and the PNN marker Wisteria Floribunda Lectin. RESULTS: We report here that PNNs are numerous and well developed in hippocampal cornu ammonis‐1 of adult males but are lower in juvenile and possibly adult females. No significant differences were observed between sexes in cornu ammonis‐3 or adjacent neocortex. There was an observed developmental difference in the neocortex as juveniles had more PVALB+ cells, but fewer PNN+ cells, than adults. CONCLUSIONS: Because PNNs are integral for several hippocampal‐mediated learning and memory tasks, these observations have potential sex‐dependent translational implications for clinical strategies targeting cognitive dysfunction. John Wiley and Sons Inc. 2019-03-25 /pmc/articles/PMC6520292/ /pubmed/30912298 http://dx.doi.org/10.1002/brb3.1265 Text en © 2019 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Griffiths, Brian B.
Madden, Amanda M. K.
Edwards, Kimbra A.
Zup, Susan L.
Stary, Creed M.
Age‐dependent sexual dimorphism in hippocampal cornu ammonis‐1 perineuronal net expression in rats
title Age‐dependent sexual dimorphism in hippocampal cornu ammonis‐1 perineuronal net expression in rats
title_full Age‐dependent sexual dimorphism in hippocampal cornu ammonis‐1 perineuronal net expression in rats
title_fullStr Age‐dependent sexual dimorphism in hippocampal cornu ammonis‐1 perineuronal net expression in rats
title_full_unstemmed Age‐dependent sexual dimorphism in hippocampal cornu ammonis‐1 perineuronal net expression in rats
title_short Age‐dependent sexual dimorphism in hippocampal cornu ammonis‐1 perineuronal net expression in rats
title_sort age‐dependent sexual dimorphism in hippocampal cornu ammonis‐1 perineuronal net expression in rats
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6520292/
https://www.ncbi.nlm.nih.gov/pubmed/30912298
http://dx.doi.org/10.1002/brb3.1265
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