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Reorganization of supramammillary–hippocampal pathways in the rat pilocarpine model of temporal lobe epilepsy: evidence for axon terminal sprouting

In mesial temporal lobe epilepsy (MTLE), spontaneous seizures likely originate from a multi-structural epileptogenic zone, including several regions of the limbic system connected to the hippocampal formation. In this study, we investigate the structural connectivity between the supramammillary nucl...

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Autores principales: Soussi, Rabia, Boulland, Jean-Luc, Bassot, Emilie, Bras, Hélène, Coulon, Patrice, Chaudhry, Farrukh Abbas, Storm-Mathisen, Jon, Ferhat, Lotfi, Esclapez, Monique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4481331/
https://www.ncbi.nlm.nih.gov/pubmed/24889162
http://dx.doi.org/10.1007/s00429-014-0800-2
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author Soussi, Rabia
Boulland, Jean-Luc
Bassot, Emilie
Bras, Hélène
Coulon, Patrice
Chaudhry, Farrukh Abbas
Storm-Mathisen, Jon
Ferhat, Lotfi
Esclapez, Monique
author_facet Soussi, Rabia
Boulland, Jean-Luc
Bassot, Emilie
Bras, Hélène
Coulon, Patrice
Chaudhry, Farrukh Abbas
Storm-Mathisen, Jon
Ferhat, Lotfi
Esclapez, Monique
author_sort Soussi, Rabia
collection PubMed
description In mesial temporal lobe epilepsy (MTLE), spontaneous seizures likely originate from a multi-structural epileptogenic zone, including several regions of the limbic system connected to the hippocampal formation. In this study, we investigate the structural connectivity between the supramammillary nucleus (SuM) and the dentate gyrus (DG) in the model of MTLE induced by pilocarpine in the rat. This hypothalamic nucleus, which provides major extracortical projections to the hippocampal formation, plays a key role in the regulation of several hippocampus-dependent activities, including theta rhythms, memory function and emotional behavior, such as stress and anxiety, functions that are known to be altered in MTLE. Our findings demonstrate a marked reorganization of DG afferents originating from the SuM in pilocarpine-treated rats. This reorganization, which starts during the latent period, is massive when animals become epileptic and continue to evolve during epilepsy. It is characterized by an aberrant distribution and an increased number of axon terminals from neurons of both lateral and medial regions of the SuM, invading the entire inner molecular layer of the DG. This reorganization, which reflects an axon terminal sprouting from SuM neurons, could contribute to trigger spontaneous seizures within an altered hippocampal intrinsic circuitry.
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spelling pubmed-44813312015-07-02 Reorganization of supramammillary–hippocampal pathways in the rat pilocarpine model of temporal lobe epilepsy: evidence for axon terminal sprouting Soussi, Rabia Boulland, Jean-Luc Bassot, Emilie Bras, Hélène Coulon, Patrice Chaudhry, Farrukh Abbas Storm-Mathisen, Jon Ferhat, Lotfi Esclapez, Monique Brain Struct Funct Original Article In mesial temporal lobe epilepsy (MTLE), spontaneous seizures likely originate from a multi-structural epileptogenic zone, including several regions of the limbic system connected to the hippocampal formation. In this study, we investigate the structural connectivity between the supramammillary nucleus (SuM) and the dentate gyrus (DG) in the model of MTLE induced by pilocarpine in the rat. This hypothalamic nucleus, which provides major extracortical projections to the hippocampal formation, plays a key role in the regulation of several hippocampus-dependent activities, including theta rhythms, memory function and emotional behavior, such as stress and anxiety, functions that are known to be altered in MTLE. Our findings demonstrate a marked reorganization of DG afferents originating from the SuM in pilocarpine-treated rats. This reorganization, which starts during the latent period, is massive when animals become epileptic and continue to evolve during epilepsy. It is characterized by an aberrant distribution and an increased number of axon terminals from neurons of both lateral and medial regions of the SuM, invading the entire inner molecular layer of the DG. This reorganization, which reflects an axon terminal sprouting from SuM neurons, could contribute to trigger spontaneous seizures within an altered hippocampal intrinsic circuitry. Springer Berlin Heidelberg 2014-06-03 2015 /pmc/articles/PMC4481331/ /pubmed/24889162 http://dx.doi.org/10.1007/s00429-014-0800-2 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Article
Soussi, Rabia
Boulland, Jean-Luc
Bassot, Emilie
Bras, Hélène
Coulon, Patrice
Chaudhry, Farrukh Abbas
Storm-Mathisen, Jon
Ferhat, Lotfi
Esclapez, Monique
Reorganization of supramammillary–hippocampal pathways in the rat pilocarpine model of temporal lobe epilepsy: evidence for axon terminal sprouting
title Reorganization of supramammillary–hippocampal pathways in the rat pilocarpine model of temporal lobe epilepsy: evidence for axon terminal sprouting
title_full Reorganization of supramammillary–hippocampal pathways in the rat pilocarpine model of temporal lobe epilepsy: evidence for axon terminal sprouting
title_fullStr Reorganization of supramammillary–hippocampal pathways in the rat pilocarpine model of temporal lobe epilepsy: evidence for axon terminal sprouting
title_full_unstemmed Reorganization of supramammillary–hippocampal pathways in the rat pilocarpine model of temporal lobe epilepsy: evidence for axon terminal sprouting
title_short Reorganization of supramammillary–hippocampal pathways in the rat pilocarpine model of temporal lobe epilepsy: evidence for axon terminal sprouting
title_sort reorganization of supramammillary–hippocampal pathways in the rat pilocarpine model of temporal lobe epilepsy: evidence for axon terminal sprouting
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4481331/
https://www.ncbi.nlm.nih.gov/pubmed/24889162
http://dx.doi.org/10.1007/s00429-014-0800-2
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