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Low-intensity ultrasound restores long-term potentiation and memory in senescent mice through pleiotropic mechanisms including NMDAR signaling
Advanced physiological aging is associated with impaired cognitive performance and the inability to induce long-term potentiation (LTP), an electrophysiological correlate of memory. Here, we demonstrate in the physiologically aged, senescent mouse brain that scanning ultrasound combined with microbu...
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/PMC8760044/ https://www.ncbi.nlm.nih.gov/pubmed/34040151 http://dx.doi.org/10.1038/s41380-021-01129-7 |
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author | Blackmore, Daniel G. Turpin, Fabrice Palliyaguru, Tishila Evans, Harrison T. Chicoteau, Antony Lee, Wendy Pelekanos, Matthew Nguyen, Nghia Song, Jae Sullivan, Robert K. P. Sah, Pankaj Bartlett, Perry F. Götz, Jürgen |
author_facet | Blackmore, Daniel G. Turpin, Fabrice Palliyaguru, Tishila Evans, Harrison T. Chicoteau, Antony Lee, Wendy Pelekanos, Matthew Nguyen, Nghia Song, Jae Sullivan, Robert K. P. Sah, Pankaj Bartlett, Perry F. Götz, Jürgen |
author_sort | Blackmore, Daniel G. |
collection | PubMed |
description | Advanced physiological aging is associated with impaired cognitive performance and the inability to induce long-term potentiation (LTP), an electrophysiological correlate of memory. Here, we demonstrate in the physiologically aged, senescent mouse brain that scanning ultrasound combined with microbubbles (SUS(+MB)), by transiently opening the blood–brain barrier, fully restores LTP induction in the dentate gyrus of the hippocampus. Intriguingly, SUS treatment without microbubbles (SUS(only)), i.e., without the uptake of blood-borne factors, proved even more effective, not only restoring LTP, but also ameliorating the spatial learning deficits of the aged mice. This functional improvement is accompanied by an altered milieu of the aged hippocampus, including a lower density of perineuronal nets, increased neurogenesis, and synaptic signaling, which collectively results in improved spatial learning. We therefore conclude that therapeutic ultrasound is a non-invasive, pleiotropic modality that may enhance cognition in elderly humans. |
format | Online Article Text |
id | pubmed-8760044 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-87600442022-01-26 Low-intensity ultrasound restores long-term potentiation and memory in senescent mice through pleiotropic mechanisms including NMDAR signaling Blackmore, Daniel G. Turpin, Fabrice Palliyaguru, Tishila Evans, Harrison T. Chicoteau, Antony Lee, Wendy Pelekanos, Matthew Nguyen, Nghia Song, Jae Sullivan, Robert K. P. Sah, Pankaj Bartlett, Perry F. Götz, Jürgen Mol Psychiatry Article Advanced physiological aging is associated with impaired cognitive performance and the inability to induce long-term potentiation (LTP), an electrophysiological correlate of memory. Here, we demonstrate in the physiologically aged, senescent mouse brain that scanning ultrasound combined with microbubbles (SUS(+MB)), by transiently opening the blood–brain barrier, fully restores LTP induction in the dentate gyrus of the hippocampus. Intriguingly, SUS treatment without microbubbles (SUS(only)), i.e., without the uptake of blood-borne factors, proved even more effective, not only restoring LTP, but also ameliorating the spatial learning deficits of the aged mice. This functional improvement is accompanied by an altered milieu of the aged hippocampus, including a lower density of perineuronal nets, increased neurogenesis, and synaptic signaling, which collectively results in improved spatial learning. We therefore conclude that therapeutic ultrasound is a non-invasive, pleiotropic modality that may enhance cognition in elderly humans. Nature Publishing Group UK 2021-05-27 2021 /pmc/articles/PMC8760044/ /pubmed/34040151 http://dx.doi.org/10.1038/s41380-021-01129-7 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 Blackmore, Daniel G. Turpin, Fabrice Palliyaguru, Tishila Evans, Harrison T. Chicoteau, Antony Lee, Wendy Pelekanos, Matthew Nguyen, Nghia Song, Jae Sullivan, Robert K. P. Sah, Pankaj Bartlett, Perry F. Götz, Jürgen Low-intensity ultrasound restores long-term potentiation and memory in senescent mice through pleiotropic mechanisms including NMDAR signaling |
title | Low-intensity ultrasound restores long-term potentiation and memory in senescent mice through pleiotropic mechanisms including NMDAR signaling |
title_full | Low-intensity ultrasound restores long-term potentiation and memory in senescent mice through pleiotropic mechanisms including NMDAR signaling |
title_fullStr | Low-intensity ultrasound restores long-term potentiation and memory in senescent mice through pleiotropic mechanisms including NMDAR signaling |
title_full_unstemmed | Low-intensity ultrasound restores long-term potentiation and memory in senescent mice through pleiotropic mechanisms including NMDAR signaling |
title_short | Low-intensity ultrasound restores long-term potentiation and memory in senescent mice through pleiotropic mechanisms including NMDAR signaling |
title_sort | low-intensity ultrasound restores long-term potentiation and memory in senescent mice through pleiotropic mechanisms including nmdar signaling |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8760044/ https://www.ncbi.nlm.nih.gov/pubmed/34040151 http://dx.doi.org/10.1038/s41380-021-01129-7 |
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