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Increased excitatory to inhibitory synaptic ratio in parietal cortex samples from individuals with Alzheimer’s disease
Synaptic disturbances in excitatory to inhibitory (E/I) balance in forebrain circuits are thought to contribute to the progression of Alzheimer’s disease (AD) and dementia, although direct evidence for such imbalance in humans is lacking. We assessed anatomical and electrophysiological synaptic E/I...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8110554/ https://www.ncbi.nlm.nih.gov/pubmed/33972518 http://dx.doi.org/10.1038/s41467-021-22742-8 |
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author | Lauterborn, Julie C. Scaduto, Pietro Cox, Conor D. Schulmann, Anton Lynch, Gary Gall, Christine M. Keene, C. Dirk Limon, Agenor |
author_facet | Lauterborn, Julie C. Scaduto, Pietro Cox, Conor D. Schulmann, Anton Lynch, Gary Gall, Christine M. Keene, C. Dirk Limon, Agenor |
author_sort | Lauterborn, Julie C. |
collection | PubMed |
description | Synaptic disturbances in excitatory to inhibitory (E/I) balance in forebrain circuits are thought to contribute to the progression of Alzheimer’s disease (AD) and dementia, although direct evidence for such imbalance in humans is lacking. We assessed anatomical and electrophysiological synaptic E/I ratios in post-mortem parietal cortex samples from middle-aged individuals with AD (early-onset) or Down syndrome (DS) by fluorescence deconvolution tomography and microtransplantation of synaptic membranes. Both approaches revealed significantly elevated E/I ratios for AD, but not DS, versus controls. Gene expression studies in an independent AD cohort also demonstrated elevated E/I ratios in individuals with AD as compared to controls. These findings provide evidence of a marked pro-excitatory perturbation of synaptic E/I balance in AD parietal cortex, a region within the default mode network that is overly active in the disorder, and support the hypothesis that E/I imbalances disrupt cognition-related shifts in cortical activity which contribute to the intellectual decline in AD. |
format | Online Article Text |
id | pubmed-8110554 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81105542021-05-11 Increased excitatory to inhibitory synaptic ratio in parietal cortex samples from individuals with Alzheimer’s disease Lauterborn, Julie C. Scaduto, Pietro Cox, Conor D. Schulmann, Anton Lynch, Gary Gall, Christine M. Keene, C. Dirk Limon, Agenor Nat Commun Article Synaptic disturbances in excitatory to inhibitory (E/I) balance in forebrain circuits are thought to contribute to the progression of Alzheimer’s disease (AD) and dementia, although direct evidence for such imbalance in humans is lacking. We assessed anatomical and electrophysiological synaptic E/I ratios in post-mortem parietal cortex samples from middle-aged individuals with AD (early-onset) or Down syndrome (DS) by fluorescence deconvolution tomography and microtransplantation of synaptic membranes. Both approaches revealed significantly elevated E/I ratios for AD, but not DS, versus controls. Gene expression studies in an independent AD cohort also demonstrated elevated E/I ratios in individuals with AD as compared to controls. These findings provide evidence of a marked pro-excitatory perturbation of synaptic E/I balance in AD parietal cortex, a region within the default mode network that is overly active in the disorder, and support the hypothesis that E/I imbalances disrupt cognition-related shifts in cortical activity which contribute to the intellectual decline in AD. Nature Publishing Group UK 2021-05-10 /pmc/articles/PMC8110554/ /pubmed/33972518 http://dx.doi.org/10.1038/s41467-021-22742-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Lauterborn, Julie C. Scaduto, Pietro Cox, Conor D. Schulmann, Anton Lynch, Gary Gall, Christine M. Keene, C. Dirk Limon, Agenor Increased excitatory to inhibitory synaptic ratio in parietal cortex samples from individuals with Alzheimer’s disease |
title | Increased excitatory to inhibitory synaptic ratio in parietal cortex samples from individuals with Alzheimer’s disease |
title_full | Increased excitatory to inhibitory synaptic ratio in parietal cortex samples from individuals with Alzheimer’s disease |
title_fullStr | Increased excitatory to inhibitory synaptic ratio in parietal cortex samples from individuals with Alzheimer’s disease |
title_full_unstemmed | Increased excitatory to inhibitory synaptic ratio in parietal cortex samples from individuals with Alzheimer’s disease |
title_short | Increased excitatory to inhibitory synaptic ratio in parietal cortex samples from individuals with Alzheimer’s disease |
title_sort | increased excitatory to inhibitory synaptic ratio in parietal cortex samples from individuals with alzheimer’s disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8110554/ https://www.ncbi.nlm.nih.gov/pubmed/33972518 http://dx.doi.org/10.1038/s41467-021-22742-8 |
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