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Abnormal Capillary Vasodynamics Contribute to Ictal Neurodegeneration in Epilepsy

Seizure-driven brain damage in epilepsy accumulates over time, especially in the hippocampus, which can lead to sclerosis, cognitive decline, and death. Excitotoxicity is the prevalent model to explain ictal neurodegeneration. Current labeling technologies cannot distinguish between excitotoxicity a...

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Autores principales: Leal-Campanario, Rocio, Alarcon-Martinez, Luis, Rieiro, Hector, Martinez-Conde, Susana, Alarcon-Martinez, Tugba, Zhao, Xiuli, LaMee, Jonathan, Popp, Pamela J. Osborn, Calhoun, Michael E., Arribas, Juan I., Schlegel, Alexander A., Stasi, Leandro L. Di, Rho, Jong M., Inge, Landon, Otero-Millan, Jorge, Treiman, David M., Macknik, Stephen L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5327474/
https://www.ncbi.nlm.nih.gov/pubmed/28240297
http://dx.doi.org/10.1038/srep43276
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author Leal-Campanario, Rocio
Alarcon-Martinez, Luis
Rieiro, Hector
Martinez-Conde, Susana
Alarcon-Martinez, Tugba
Zhao, Xiuli
LaMee, Jonathan
Popp, Pamela J. Osborn
Calhoun, Michael E.
Arribas, Juan I.
Schlegel, Alexander A.
Stasi, Leandro L. Di
Rho, Jong M.
Inge, Landon
Otero-Millan, Jorge
Treiman, David M.
Macknik, Stephen L.
author_facet Leal-Campanario, Rocio
Alarcon-Martinez, Luis
Rieiro, Hector
Martinez-Conde, Susana
Alarcon-Martinez, Tugba
Zhao, Xiuli
LaMee, Jonathan
Popp, Pamela J. Osborn
Calhoun, Michael E.
Arribas, Juan I.
Schlegel, Alexander A.
Stasi, Leandro L. Di
Rho, Jong M.
Inge, Landon
Otero-Millan, Jorge
Treiman, David M.
Macknik, Stephen L.
author_sort Leal-Campanario, Rocio
collection PubMed
description Seizure-driven brain damage in epilepsy accumulates over time, especially in the hippocampus, which can lead to sclerosis, cognitive decline, and death. Excitotoxicity is the prevalent model to explain ictal neurodegeneration. Current labeling technologies cannot distinguish between excitotoxicity and hypoxia, however, because they share common molecular mechanisms. This leaves open the possibility that undetected ischemic hypoxia, due to ictal blood flow restriction, could contribute to neurodegeneration previously ascribed to excitotoxicity. We tested this possibility with Confocal Laser Endomicroscopy (CLE) and novel stereological analyses in several models of epileptic mice. We found a higher number and magnitude of NG2+ mural-cell mediated capillary constrictions in the hippocampus of epileptic mice than in that of normal mice, in addition to spatial coupling between capillary constrictions and oxidative stressed neurons and neurodegeneration. These results reveal a role for hypoxia driven by capillary blood flow restriction in ictal neurodegeneration.
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spelling pubmed-53274742017-03-03 Abnormal Capillary Vasodynamics Contribute to Ictal Neurodegeneration in Epilepsy Leal-Campanario, Rocio Alarcon-Martinez, Luis Rieiro, Hector Martinez-Conde, Susana Alarcon-Martinez, Tugba Zhao, Xiuli LaMee, Jonathan Popp, Pamela J. Osborn Calhoun, Michael E. Arribas, Juan I. Schlegel, Alexander A. Stasi, Leandro L. Di Rho, Jong M. Inge, Landon Otero-Millan, Jorge Treiman, David M. Macknik, Stephen L. Sci Rep Article Seizure-driven brain damage in epilepsy accumulates over time, especially in the hippocampus, which can lead to sclerosis, cognitive decline, and death. Excitotoxicity is the prevalent model to explain ictal neurodegeneration. Current labeling technologies cannot distinguish between excitotoxicity and hypoxia, however, because they share common molecular mechanisms. This leaves open the possibility that undetected ischemic hypoxia, due to ictal blood flow restriction, could contribute to neurodegeneration previously ascribed to excitotoxicity. We tested this possibility with Confocal Laser Endomicroscopy (CLE) and novel stereological analyses in several models of epileptic mice. We found a higher number and magnitude of NG2+ mural-cell mediated capillary constrictions in the hippocampus of epileptic mice than in that of normal mice, in addition to spatial coupling between capillary constrictions and oxidative stressed neurons and neurodegeneration. These results reveal a role for hypoxia driven by capillary blood flow restriction in ictal neurodegeneration. Nature Publishing Group 2017-02-27 /pmc/articles/PMC5327474/ /pubmed/28240297 http://dx.doi.org/10.1038/srep43276 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Leal-Campanario, Rocio
Alarcon-Martinez, Luis
Rieiro, Hector
Martinez-Conde, Susana
Alarcon-Martinez, Tugba
Zhao, Xiuli
LaMee, Jonathan
Popp, Pamela J. Osborn
Calhoun, Michael E.
Arribas, Juan I.
Schlegel, Alexander A.
Stasi, Leandro L. Di
Rho, Jong M.
Inge, Landon
Otero-Millan, Jorge
Treiman, David M.
Macknik, Stephen L.
Abnormal Capillary Vasodynamics Contribute to Ictal Neurodegeneration in Epilepsy
title Abnormal Capillary Vasodynamics Contribute to Ictal Neurodegeneration in Epilepsy
title_full Abnormal Capillary Vasodynamics Contribute to Ictal Neurodegeneration in Epilepsy
title_fullStr Abnormal Capillary Vasodynamics Contribute to Ictal Neurodegeneration in Epilepsy
title_full_unstemmed Abnormal Capillary Vasodynamics Contribute to Ictal Neurodegeneration in Epilepsy
title_short Abnormal Capillary Vasodynamics Contribute to Ictal Neurodegeneration in Epilepsy
title_sort abnormal capillary vasodynamics contribute to ictal neurodegeneration in epilepsy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5327474/
https://www.ncbi.nlm.nih.gov/pubmed/28240297
http://dx.doi.org/10.1038/srep43276
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