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Microbial memories: Sex‐dependent impact of the gut microbiome on hippocampal plasticity

Germ‐free rodents, raised in the absence of a measurable gut microbiome, have been a key model to study the microbiome‐gut‐brain axis. Germ‐free mice exhibit marked behavioural and neurochemical differences to their conventionally raised counterparts. It is as yet unclear how these neurochemical dif...

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Autores principales: Darch, Henry T., Collins, Michael K., O’Riordan, Kenneth J., Cryan, John F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8451864/
https://www.ncbi.nlm.nih.gov/pubmed/33458858
http://dx.doi.org/10.1111/ejn.15119
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author Darch, Henry T.
Collins, Michael K.
O’Riordan, Kenneth J.
Cryan, John F.
author_facet Darch, Henry T.
Collins, Michael K.
O’Riordan, Kenneth J.
Cryan, John F.
author_sort Darch, Henry T.
collection PubMed
description Germ‐free rodents, raised in the absence of a measurable gut microbiome, have been a key model to study the microbiome‐gut‐brain axis. Germ‐free mice exhibit marked behavioural and neurochemical differences to their conventionally raised counterparts. It is as yet unclear how these neurochemical differences lead to the behavioural differences. Here, we test the electrophysiological properties of hippocampal plasticity in adult germ‐free mice and compare them to conventionally raised counterparts. Whilst basal synaptic efficacy and pre‐synaptic short‐term plasticity appear normal, we find a striking alteration of hippocampal long‐term potentiation specifically in male germ‐free slices. However, the spike output of these neurons remains normal along with altered input‐output coupling, potentially indicating homeostatic compensatory mechanisms, or an altered excitation/inhibition balance. To our knowledge this is the first time the electrophysiological properties of the hippocampus have been assessed in a microbiome deficient animal. Our data indicate that the absence of a microbiome alters integration of dendritic signalling in the CA1 region in mice.
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spelling pubmed-84518642021-09-27 Microbial memories: Sex‐dependent impact of the gut microbiome on hippocampal plasticity Darch, Henry T. Collins, Michael K. O’Riordan, Kenneth J. Cryan, John F. Eur J Neurosci Molecular and Synaptic Mechanisms Germ‐free rodents, raised in the absence of a measurable gut microbiome, have been a key model to study the microbiome‐gut‐brain axis. Germ‐free mice exhibit marked behavioural and neurochemical differences to their conventionally raised counterparts. It is as yet unclear how these neurochemical differences lead to the behavioural differences. Here, we test the electrophysiological properties of hippocampal plasticity in adult germ‐free mice and compare them to conventionally raised counterparts. Whilst basal synaptic efficacy and pre‐synaptic short‐term plasticity appear normal, we find a striking alteration of hippocampal long‐term potentiation specifically in male germ‐free slices. However, the spike output of these neurons remains normal along with altered input‐output coupling, potentially indicating homeostatic compensatory mechanisms, or an altered excitation/inhibition balance. To our knowledge this is the first time the electrophysiological properties of the hippocampus have been assessed in a microbiome deficient animal. Our data indicate that the absence of a microbiome alters integration of dendritic signalling in the CA1 region in mice. John Wiley and Sons Inc. 2021-02-01 2021-08 /pmc/articles/PMC8451864/ /pubmed/33458858 http://dx.doi.org/10.1111/ejn.15119 Text en © 2021 The Authors. European Journal of Neuroscience published by Federation of European Neuroscience Societies and John Wiley & Sons Ltd. 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 Molecular and Synaptic Mechanisms
Darch, Henry T.
Collins, Michael K.
O’Riordan, Kenneth J.
Cryan, John F.
Microbial memories: Sex‐dependent impact of the gut microbiome on hippocampal plasticity
title Microbial memories: Sex‐dependent impact of the gut microbiome on hippocampal plasticity
title_full Microbial memories: Sex‐dependent impact of the gut microbiome on hippocampal plasticity
title_fullStr Microbial memories: Sex‐dependent impact of the gut microbiome on hippocampal plasticity
title_full_unstemmed Microbial memories: Sex‐dependent impact of the gut microbiome on hippocampal plasticity
title_short Microbial memories: Sex‐dependent impact of the gut microbiome on hippocampal plasticity
title_sort microbial memories: sex‐dependent impact of the gut microbiome on hippocampal plasticity
topic Molecular and Synaptic Mechanisms
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8451864/
https://www.ncbi.nlm.nih.gov/pubmed/33458858
http://dx.doi.org/10.1111/ejn.15119
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