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Spatial contribution of hippocampal BOLD activation in high-resolution fMRI
While the vascular origin of the BOLD-fMRI signal is established, the exact neurovascular coupling events contributing to this signal are still incompletely understood. Furthermore, the hippocampal spatial properties of the BOLD activation are not elucidated, although electrophysiology approaches ha...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6395694/ https://www.ncbi.nlm.nih.gov/pubmed/30816226 http://dx.doi.org/10.1038/s41598-019-39614-3 |
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author | Abe, Yoshifumi Tsurugizawa, Tomokazu Le Bihan, Denis Ciobanu, Luisa |
author_facet | Abe, Yoshifumi Tsurugizawa, Tomokazu Le Bihan, Denis Ciobanu, Luisa |
author_sort | Abe, Yoshifumi |
collection | PubMed |
description | While the vascular origin of the BOLD-fMRI signal is established, the exact neurovascular coupling events contributing to this signal are still incompletely understood. Furthermore, the hippocampal spatial properties of the BOLD activation are not elucidated, although electrophysiology approaches have already revealed the precise spatial patterns of neural activity. High magnetic field fMRI offers improved contrast and allows for a better correlation with the underlying neuronal activity because of the increased contribution to the BOLD signal of small blood vessels. Here, we take advantage of these two benefits to investigate the spatial characteristics of the hippocampal activation in a rat model before and after changing the hippocampal plasticity by long-term potentiation (LTP). We found that the hippocampal BOLD signals evoked by electrical stimulation at the perforant pathway increased more at the radiatum layer of the hippocampal CA1 region than at the pyramidal cell layer. The return to the baseline of the hippocampal BOLD activation was prolonged after LTP induction compared with that before most likely due vascular or neurovascular coupling changes. Based on these results, we conclude that high resolution BOLD-fMRI allows the segregation of hippocampal subfields probably based on their underlying vascular or neurovascular coupling features. |
format | Online Article Text |
id | pubmed-6395694 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63956942019-03-04 Spatial contribution of hippocampal BOLD activation in high-resolution fMRI Abe, Yoshifumi Tsurugizawa, Tomokazu Le Bihan, Denis Ciobanu, Luisa Sci Rep Article While the vascular origin of the BOLD-fMRI signal is established, the exact neurovascular coupling events contributing to this signal are still incompletely understood. Furthermore, the hippocampal spatial properties of the BOLD activation are not elucidated, although electrophysiology approaches have already revealed the precise spatial patterns of neural activity. High magnetic field fMRI offers improved contrast and allows for a better correlation with the underlying neuronal activity because of the increased contribution to the BOLD signal of small blood vessels. Here, we take advantage of these two benefits to investigate the spatial characteristics of the hippocampal activation in a rat model before and after changing the hippocampal plasticity by long-term potentiation (LTP). We found that the hippocampal BOLD signals evoked by electrical stimulation at the perforant pathway increased more at the radiatum layer of the hippocampal CA1 region than at the pyramidal cell layer. The return to the baseline of the hippocampal BOLD activation was prolonged after LTP induction compared with that before most likely due vascular or neurovascular coupling changes. Based on these results, we conclude that high resolution BOLD-fMRI allows the segregation of hippocampal subfields probably based on their underlying vascular or neurovascular coupling features. Nature Publishing Group UK 2019-02-28 /pmc/articles/PMC6395694/ /pubmed/30816226 http://dx.doi.org/10.1038/s41598-019-39614-3 Text en © The Author(s) 2019 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/. |
spellingShingle | Article Abe, Yoshifumi Tsurugizawa, Tomokazu Le Bihan, Denis Ciobanu, Luisa Spatial contribution of hippocampal BOLD activation in high-resolution fMRI |
title | Spatial contribution of hippocampal BOLD activation in high-resolution fMRI |
title_full | Spatial contribution of hippocampal BOLD activation in high-resolution fMRI |
title_fullStr | Spatial contribution of hippocampal BOLD activation in high-resolution fMRI |
title_full_unstemmed | Spatial contribution of hippocampal BOLD activation in high-resolution fMRI |
title_short | Spatial contribution of hippocampal BOLD activation in high-resolution fMRI |
title_sort | spatial contribution of hippocampal bold activation in high-resolution fmri |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6395694/ https://www.ncbi.nlm.nih.gov/pubmed/30816226 http://dx.doi.org/10.1038/s41598-019-39614-3 |
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